Pancreatic ductal adenocarcinoma (PDAC), a highly invasive tumor that arises from the epithelial cells lining the pancreatic duct and constitutes ~80–90% of total pancreatic cancer (PC) cases (1,2). According to the GLOBOCAN 2022 data, there were a total of 510,566 newly diagnosed cases of PC worldwide in 2022, positioning it as the twelfth most prevalent malignancy globally (3). Due to its insidious onset, diagnosing early stages of PDAC presents challenges. Most patients with this condition typically experience upper abdominal discomfort or exhibit initial symptoms such as dull pain and swelling.

Currently, the diagnosis of PDAC primarily relies on imaging examinations, complemented by the detection of serum biomarker carbohydrate antigen 19-9 (CA19-9) (4). The clinical diagnosis of PDAC often occurs at an advanced or even metastatic stage, primarily due to its low specificity and aggressive progression (5). The lack of efficacious targeted drugs further contributes to the suboptimal clinical diagnosis and prognosis of PDAC. Therefore, it is imperative to enhance early diagnostic and therapeutic approaches in order to improve the overall prognosis of PDAC (6). The activation of proto-oncogenes has been increasingly found to induce cancer cells to release a higher quantity of exosomes compared with healthy cells. This phenomenon significantly impacts the progression of PDAC through its transmission in both the tumor microenvironment (TME) and the entire body (7,8). Therefore, exosomes could be considered as promising diagnostic biomarkers for tumors, including PDAC (9–11).

Studies have explored the utility of exosomal markers such as B7-H4, Plectin-1, SATB2, Glypican-1 and microRNAs (miRNAs or miRs) in diagnosing PDAC and other related neoplasms (11–14). These exosomal markers have demonstrated potential in distinguishing between different types of PC, aiding in the accurate identification of malignant pancreatic intraductal papillary mucinous neoplasms and cholangiocarcinoma (15). Despite the challenges in validation, the use of exosomes as non-invasive diagnostic biomarkers is essential for the early detection of PDAC, a disease often diagnosed late due to its asymptomatic nature (16,17).

The ability of exosomes to transfer chemical agents has garnered significant interest across various fields. A study conducted by Zheng et al (18) demonstrated the protective effects of transplantation of mesenchymal stem cell-derived exosomes against Dox-induced cardiomyopathy. Chen et al (19) proposed that plant exosome-like nanovesicles (PENVs) and artificial PENV-derived nano-vectors hold immense potential for efficient delivery of therapeutic small RNA in mammalian systems, thereby showcasing promising prospects for future clinical applications. A previous study by Tamura et al (20) on the Myristoylated Alanine-Rich C-kinase Substrate (MARCKS)-ED-photodoxaz system presents a novel and promising approach for cancer treatment through targeted manipulation of exosomes and utilization of photochemistry. Kreger et al (21) reported that enrichment of Survivin in breast cancer (BRCA) cell-derived exosomes treated with Paclitaxel (PTX) promotes cellular survival and enhances resistance to chemotherapy. Additionally, engineered exosomes have been found to possess the ability to directly target cancer cells by transporting gemcitabine (GEM), PTX and other chemical agents (22). Overall, the literature suggests that exosomes possess the capability to transfer various molecules between cells, highlighting their potential in fields such as immunology, imaging and targeted therapy (23).

At present, there have been some reviews on the exosomes and PC (24–36). A review from Ariston Gabriel et al (31) in 2020 emphasizes the crucial significance of exosomes in both PC early diagnosis and treatment through involving in metastasis, cell proliferation, epithelial-mesenchymal transition (EMT), angiogenesis and TME of PC (31). In 2023, Fang et al (32) presented a comprehensive analysis elucidating the involvement of tumor-derived exosomes in various aspects of PC progression, including developing, progressing, diagnosing, monitoring and treating. Furthermore, the study of Bunduc et al (33) on utilizing exosomes for prognostic assessment in PDAC provides valuable perspectives. Expanding upon these findings, the classification of exosomes and their diverse mechanisms for diagnostic purposes are further reviewed, and the latest advancements in utilizing exosomes for the diagnosis and monitoring of PDAC are elaborated. Different from previous reviews that provide an overall summary of the role of exosomes in PC proliferation, invasion and metastasis, the present review lays out the roles of different types of bioactive molecules carried by exosomes including mRNA, miRNA, long non-coding RNA (lncRNA), circular RNA (circRNA), DNA and protein in early screening of PDAC. Additionally, the present review delves into the potential clinical applications of exosomes as efficacious drug delivery tools and the newly discovered bacterial exosomes are discussed. The current analysis further enhances this perspective by elucidating the early diagnosis and treatment potential of exosomes, thereby providing a comprehensive overview of recent advancements in utilizing exosomes for PDAC diagnosis and treatment.

Extracellular vesicles (EVs) are a type of cell-secreted vesicles with a membrane structure, which can be categorized into three main groups based on their size, biological characteristics and formation process: Exosomes, microvesicles and apoptotic bodies (37,38). Exosomes typically refer to microvesicles with a diameter ranging from 30 to 150 nm that are formed through the fusion of multivesicular bodies (MVBs) with the cell membrane. In general, exosome biogenesis occurs through endosomal secretion in the early stages, facilitated by cytoplasmic membrane invagination within endocytic vesicles and subsequent multiplication during small body engulfment due to gradual lipid membrane fusion, resulting in the formation of early endosomes. During the process of endosome maturation, intracellular materials continue to be internalized by the cell membrane, leading to the formation of multiple luminal vesicles (ILVs), which eventually transform into MVBs. Finally, MVBs give rise to exosomes through their fusion with the plasma membrane and subsequent exocytosis of ILVs towards the extracellular space (39–41).

The secretion and release of exosomes is a precisely regulated process, with the involvement of various proteins such as Alix and TSG101 in exosome formation (42). Additionally, due to their role in signal transmission, the surface of exosomes typically contains four transmembrane proteins, including CD9, CD63 and CD81 (43). In addition to specific proteins, the phospholipid bilayer membrane of exosomes primarily comprises lipids and phospholipids, which are abundant in substances such as cholesterol, ceramide and sphingomyelin (44). The interaction between exosomes and cell surface receptors typically occurs through transmembrane proteins or lipid ligands, facilitating the delivery of exosomes and their internal proteins or nucleic acids to recipient cells via endocytosis (45). Therefore, exosomes play a crucial role in intercellular communication and are indispensable for the development and progression of diseases (23,46). Moreover, exosomes are abundantly present in various body fluids (47,48). It has been confirmed that all cells have the ability to secrete exosomes (49). Cancer cells in patients with PDAC can transmit bioactive molecules through exosomes, thereby disrupting the gene expression signals of neighboring stroma or epithelium and other healthy cells. Compared with individuals without cancer, cancer cells in patients with PDAC have the ability to produce a significant quantity of diverse exosomes. Once identified, isolated and characterized using conventional methods, these exosomes can serve as potential biomarkers (50,51).

Recent advancements in exosome research have diversified the techniques available for isolation and purification, each with distinct advantages and limitations influencing their suitability for clinical applications. The conventional method for exosome purification is differential centrifugation, which has been considered the ‘gold standard’. However, Lobb et al (52) demonstrated that a combination of ultrafiltration and size exclusion chromatography (SEC) can achieve comparable particle purity to density gradient purification and efficiently isolate a large quantity of exosomes from both cell culture media and human plasma. Tang et al (53) reported that ultracentrifugation exhibits the lowest yield and recovery but offers the highest protein purity compared with the other two exosome isolation methods (ExoQuick and Total Exosome Isolation Reagent). Vaswani et al (54) developed a robust protocol combining ultracentrifugation and SEC for isolating exosomes from human and bovine milk. Additionally, Tayebi et al (55) introduced an innovative approach in exosome research by integrating affinity-based methods with passive microfluidic particle trapping techniques. They utilized streptavidin-coated microbeads and biotinylated antibodies for targeted exosome capture, thereby enhancing isolation specificity. This method significantly reduces background noise during fluorescence-based quantification, though its dependency on specific antigen-antibody interactions may limit broader applicability. The diversity of these methodologies illustrates the ongoing evolution of exosome isolation and purification techniques, each contributing uniquely to the field's understanding and potential clinical applications.

TME plays a pivotal role in the progression of cancer and the failure of therapy (56). Tumor-associated macrophages (TAMs) are recruited to the TME and have been demonstrated to exert influence on cancer progression (57). Exosomes, nano-sized bio-vesicles released into bodily fluids, have been implicated in shaping the TME and contributing to cancer advancement (58). Macrophage-derived exosomal miR-501-3p has been shown to promote PDAC progression (59). A previous study has demonstrated the presence of glypican-1 (GPC1) positive exosomes in the serum of patients diagnosed with PDAC, exhibiting remarkable specificity and sensitivity. Moreover, these exosomes have shown potential in distinguishing individuals with benign pancreatic diseases or healthy subjects from those afflicted by both early and late-stage PDAC (22). Furthermore, TAMs are resident innate immune cells within the TME that actively contribute to tumor development and progression (60). The metabolic regulation governing heterogeneity among TAMs and their modulation by the TME remain areas necessitating further investigation (61). Overall, exosomes derived from macrophages play a significant role in shaping PDAC advancement as well as influencing dynamics within the TME itself (57,59). Extensive prior research has demonstrated that macrophages and fibroblasts within the TME participate in various stages of tumor development through diverse pathways (62). By engaging in bidirectional signaling with tumor cells and other cells via cancer-associated fibroblast (CAF)-derived cytokines, chemokines, growth factors and exosomes within the TME, CAFs not only promote tumor proliferation but also induce immune evasion of cancer cells. Exosomes derived from macrophages play a crucial role in the progression of PDAC and contribute to the dynamics of the TME by promoting M2 macrophage polarization. Exosomes originating from lung tumor cells, hepatocellular carcinoma (HCC) cells and Schistosoma japonicum adult worms have demonstrated their ability to modulate transcriptional and bioenergetic profiles of macrophages, inducing their polarization towards an M2 phenotype (63,64). These findings provide compelling evidence for a novel function played by exosomes in driving M2 macrophage polarization, thereby offering promising therapeutic targets for immunotherapy against lung cancer, HCC and PDAC (65,66). These findings underscore both the potential of targeting exosomes and TAMs for cancer therapy as well as emphasize the importance of comprehending their roles in driving cancer progression (67,68).

Furthermore, exosomes have the ability to transport and deliver diverse biological substances (69,70), thereby specifically targeting cancer cells or genes implicated in PDAC development. Consequently, engineered exosomes carrying specific targeted genes can be harnessed for the treatment of PDAC, thus playing a pivotal role in its therapeutic approach (71).

Exosomes have emerged as a promising non-viral delivery system for CRISPR/Cas9 gene editing in PDAC. McAndrews et al (72) demonstrated the ability of exosomes to encapsulate CRISPR/Cas9 plasmid DNA and efficiently deliver it to recipient cancer cells, thereby inducing targeted gene deletion. This approach has been shown to effectively suppress proliferation and inhibit tumor growth in preclinical models of PDAC. The objective of Su et al (73) was to elucidate the mechanisms underlying exosome-mediated intercellular communication between PC (Panc-1) cells and macrophages (J771.A1) using a Transwell co-culture system. Based on these findings, targeted genetic therapies aimed at selectively manipulating the content of tumor cell-derived exosomes, exhibiting significant potential for cancer therapy.

Exosomal heat shock protein 60 plays a pivotal role in intercellular communication, particularly in the progression of cancer (74). It holds potential clinical applications as a biomarker for diagnostics, prognostic assessment, and monitoring disease progression and treatment response in cancer. Moreover, heat shock protein 70 is upregulated in PDAC cells and inhibits caspase-dependent apoptosis, thereby facilitating cell survival (75). Heat Shock Factor 1, a protein that governs the heat shock response pathway, represents a promising target for drug intervention in cancer and proteinopathy with significant implications for therapeutic strategies and prognoses (76).

In a study conducted by Jin et al (77), it was discovered that exosomal ZIP4 promotes the growth of PDAC and serves as a novel diagnostic biomarker for this disease. Another study by Castillo et al (78) involved a comprehensive profiling of the ‘surfaceome’ of PDAC exosomes to identify surface proteins that could facilitate the enrichment of cancer-derived exosomes in liquid biopsies for subsequent molecular profiling. These studies suggest that utilizing small molecule inhibitors delivered via exosomes may offer potential therapeutic and diagnostic options for PDAC.

Exosomal nanoparticles secreted by human pancreatic tumor cell lines exert an inhibitory effect on tumor cell proliferation through the mitochondria-dependent apoptotic pathway, mediated by the activation of phosphatase and tensin homolog deleted on chromosome 10 (PTEN) and glycogen synthase kinase-3β (GSK-3β) (79). The interaction between exosomal nanoparticles and cells is considered to involve membrane lipid rafts. This interaction leads to a downregulation in the expression of hairy and enhancer-of-split homolog-1 (Hes-1), a key intranuclear target of the Notch-1 signaling pathway, as well as induction of apoptosis following G0/G1 phase cell cycle arrest (80,81). Unexpectedly, blocking presenilin results in PTEN and GSK-3β activation. Conversely, inhibition of either PTEN or GSK-3β increases Hes-1 expression and partially counteracts the proliferation inhibition induced by exosomal nanoparticles, highlighting reciprocal regulations between Notch signaling and PTEN/GSK-3β (82).

The present review focuses on the latest advancements concerning exosomes in early screening and treatment of PDAC. The aforementioned exosomes-related content was summarized to explain the roles of exosomes (Fig. 1).

A wide range of studies have consistently demonstrated that exosomes participate in cellular processes such as cell migration, invasion, immune regulation, angiogenesis and cancer cell metastasis (83–85). During PDAC progression, malignant tumor cells release exosomes that exhibit a dual function. They not only facilitate cancer growth but also stimulate fibroblasts within the TME, resulting in alterations in immune cell subtypes among host cells (86,87). Consequently, this process hampers effective targeting of immunocytes towards cancer cells while simultaneously upregulating immunocyte apoptosis' levels.

On the one hand, exosomes that promote the progression of PDAC may serve as specific diagnostic markers and therapeutic targets. Jin et al (77) discovered that exosomes derived from PC-1.0 (a highly malignant pancreatic cell line) cells can be internalized by and enhance the proliferation, migration and invasion abilities of PC-1 (a moderately malignant PC line) cells. Wang et al (88) found that hypoxic exosomes derived from PC cells activate macrophages to adopt the M2 phenotype in a HIF1α or HIF2α-dependent manner, thereby facilitating the migration, invasion and EMT of PC cells. Chiba et al (89) demonstrated through in vitro analyses that exosomes released from PC (PK-45H) cells induce various gene expressions in human umbilical vein endothelial cells (89). These findings suggest that exosomes released from PC cells may serve as novel promoters of angiogenesis. Furthermore, exosomes play a crucial role in the TME and mediate communication between PDAC cells and matrix components such as pancreatic stellate cells, regulating the progression of PDAC (90). Zhou et al (91) confirmed that exosomes derived from PDAC cells can stimulate lymphangiogenesis both in vitro and in vivo. This mechanism is related to downregulation of ABHD11 antisense RNA 1 expression in lymphatic endothelial cells and enhancement of their proliferative capacity, migratory potential and tube formation ability (91).

On the other hand, exosomes that inhibit the progression of PDAC could also be utilized as carriers for drug delivery. For instance, exosomal miR-485-3p derived from pancreatic ductal epithelial cells suppresses PDAC metastasis by targeting p21-activated kinase-1 (92). The miR let-7b-5p is highly enriched in exosomes derived from NK cells and actively contributes to their antitumor effects against PDAC cells (93). In addition, exosomal miR-3607-3p derived from natural killer cells inhibits the progression of PDAC by targeting IL-26 (94). The downregulation of lncRNA SBF2-AS1 in M2 macrophage-derived exosomes leads to an increase in miR-122-5p, which restricts X-linked inhibitor of apoptosis protein and limits the development of PDAC (95). The suppression of pancreatic ductal cell carcinoma is achieved by human umbilical cord mesenchymal stem cell-derived exosomes carrying hsa-miRNA-128-3p, which exert their inhibitory effects on Galectin-3 (96). The specific mechanism underlying the dual nature of exosomes remains to be elucidated, potentially attributed to their diverse origins.

The early stage of PDAC, characterized by a high degree of malignancy, often presents without evident clinical manifestations. As the disease progresses, patients commonly experience symptoms such as unexplained weight loss, tenderness in the upper abdomen and jaundice. Consequently, clinicians typically rely on these symptomatic presentations for diagnosing PDAC (97,98).

In clinical practice, following the assessment of genetic history and conducting a physical examination, clinicians commonly utilize blood tumor markers for the diagnosis of PDAC. Prominent diagnostic markers include CA19-9, carcinoembryonic antigen (CEA) and CA125. Among these, CA19-9 exhibits a specificity ranging from 80–90% in patients with PDAC and is considered the most sensitive tumor marker for diagnosing PDAC (99,100). However, based on scientific research, it has been observed that the CA19-9 biomarker may produce false positive outcomes in conditions such as cholangitis, inflammation and biliary tract obstruction, thereby compromising its accuracy in indicating the presence of a tumor (101). Moreover, ~15–25% of patients with early-stage PDAC exhibit CA19-9 levels below the clinical threshold of 37 U/ml (102), while Lewis antigen-negative individuals within the general population (5–10%) do not produce CA19-9 at all (102). Furthermore, achieving early detection and prompt treatment through these aforementioned methods remains challenging due to the relatively concealed pathogenesis of most cases (103). According to research findings, a significant proportion of patients receive their diagnosis when the disease has already progressed to either the intermediate or advanced stages. Consequently, there is a risk of overlooking potential opportunities for administering optimal treatment by relying solely on conventional diagnostic methods (104). Therefore, in accordance with the recommendations outlined in the latest literature, comprehensive diagnosis of PDAC includes utilization of the CA19-9 marker alongside histopathology, imaging techniques and other biomarkers (105,106). Recent studies have indicated that PDAC occurrence involves multitude cytokines, including miRNA, mRNA, DNA and exosomes (107,108). Given their detectability during PDAC development, exosomes hold great potential as diagnostic biomarkers for this disease (109).

The levels of exosomes were quantified in patients with PDAC, and the results revealed a statistically significant elevation compared with that observed in healthy controls. Additionally, there was a positive correlation between exosome levels and elevated serum CEA concentrations. Further analysis revealed a significant association between higher exosome levels, lower tumor differentiation and shorter overall survival (110). Exosome levels in PDAC vary across different stages and are correlated with disease severity (111). Significant variations in exosomal miR-10b levels among different stages of PDAC have been previously demonstrated (112). Furthermore, exosome-mediated communication contributes to the development of liver metastases in PDAC. However, comprehensive demonstration and validation are still required to establish the diagnostic validity and accuracy of exosomes for PDAC (113).

Simultaneously, bioactive molecules carried by PDAC promote cell migration and invasion (45,114); upon absorption by cancer cells, the physiological state of these cells undergoes changes leading to metastasis and spread to other parts of the body (115). Therefore, different types of bioactive molecules carried by exosomes including mRNA, miRNA, lncRNA, circRNA, DNA and protein can partially reflect the extent of tumor lesions in patients with PDAC; thus they can serve as biomarkers for early liquid biopsy screening for PDAC (33,116–118).

The optimal treatment for PDAC is surgical intervention; however, a significant proportion of patients with PDAC (~80%) fail to meet the necessary criteria for surgery, necessitating reliance on conservative pharmacotherapy instead (141,142). Currently, primary treatment options for PDAC are GEM in combination with albumin-bound PTX, GnP, FOLFIRINOX [a regimen comprising 5-fluorouracil (5-FU), leucovorin, irinotecan and oxaliplatin], and modified FOLFIRINOX (mFOLFIRINOX). The Phase III trial demonstrated that the combination of nanoparticle albumin-bound PTX and GEM significantly enhanced overall survival, progression-free survival, and response rate in patients with PDAC. However, it was associated with an increased occurrence of peripheral neuropathy and myelosuppression (143). Conroy et al (144) revealed that FOLFIRINOX exhibited a significant survival benefit compared with GEM, albeit with an increased incidence of adverse effects. Furthermore, another study highlighted that the administration of mFOLFIRINOX, as opposed to FOLFIRINOX, may lead to a reduced frequency of Grade 3 or 4 non-hematological adverse events while maintaining a comparable response rate (145).

In the NCCN 2023 guidelines for PDAC, the aforementioned traditional therapies remain commonly used, while new immunotherapy and targeted therapy options have been proposed, including the KRAS inhibitor sotorasib and BRCA inhibitor olaparib (146–148). Although not included in the list of recommended therapies, exosome therapy has shown promise in prolonging survival through its effects on immune response, angiogenesis, drug resistance of tumor cells and other mechanisms.

In PDAC, mutations in KRAS are frequently observed and have been shown to promote aggressive phenotypes (149,150). In the CodeBreaK 100 trial conducted by Strickler et al (147), the administration of KRAS G12D inhibitor sotorasib primarily resulted in mild adverse reactions among heavily pretreated populations, with safety outcomes consistent with previous reports from the same trial. KRAS mutations play a crucial role in promoting lymphangiogenesis through exosomes in PC (151). Chang et al (152) presented a comprehensive investigation into the role of exosomes in facilitating cell survival driven by KRAS mutations, revealing that KRAS-mutant cells secrete exosomes enriched with the anti-apoptotic protein Survivin. This enrichment not only enhances the survival of neighboring cells but also contributes to the overall therapeutic resistance observed in KRAS-mutant tumors. Their findings suggest that these exosomes act as mediators of intercellular communication, promoting a supportive microenvironment for tumor growth and survival. Furthermore, combining exosomes with other therapies can modulate the pathological progression of PDAC and improve treatment effectiveness. The combination of nano-liposomal irinotecan with FU and folinic acid significantly enhances survival and quality of life in patients with metastatic PDAC post-GEM therapy, highlighting its efficacy and favorable safety profile (153–155).

Several studies have demonstrated that exosomes derived from various cell sources, including immune cells and mesenchymal stem cells, are capable of carrying and delivering a diverse range of biological substances. Additionally, they can specifically target PDAC cells or participate in the progression of PDAC. This phenomenon significantly influences the advancement and invasiveness of PDAC, underscoring its crucial role in the treatment of this disease. Exosomes originating from immune cells such as dendritic cells, T cells and B cells primarily serve vital functions in facilitating the transfer of proteins, nucleic acids and lipids between cells while contributing to intercellular communication and immune regulation (156,157). Meanwhile, exosomes have been demonstrated to possess unique bioactive molecules such as major histocompatibility complex (MHC) and costimulatory molecules, which play a crucial role in mediating immune responses against cancer (158). Current studies have demonstrated that immune exosomes primarily impact the progression of PDAC by modulating immune responses within the TME. In addition to being secreted by PDAC cells, a majority of existing research (159,160) indicates that exosomes are commonly released by mesenchymal stem cells, which possess convenient accessibility and exhibit both immunogenic and immunomodulatory properties (161). Moreover, several studies have demonstrated the active migration of mesenchymal stem cells to sites of inflammation and their ability to modulate immune responses. Furthermore, it has been observed that paracrine exosomes predominantly convey biological information rather than direct cell contact (162,163). For example, umbilical cord stem cells possess robust potential in regulating tissue differentiation and regeneration due to their strong stem cell capacity (164). The exosomes can additionally regulate the TME by exerting regulatory control over angiogenesis and proliferation of PDAC cells within the TME (165). Adipose mesenchymal stem cells are more likely to play a pivotal role in immunomodulation and anti-inflammatory processes, as their exosomes have the ability to regulate the expression of interleukin 6, interleukin 10, and tumour necrosis factor alpha, thereby participating in immune modulation and inflammation regulation in vivo (166,167). For instance, Liu et al (168) demonstrated that exosomes derived from adipose-derived mesenchymal stem cells can mitigate oxidative stress, inflammation and infiltration of microglial cells through the activation of the silent information regulator sirtuin 1 pathway. Therefore, exosomes derived from diverse cellular origins exert a regulatory influence on the progression of PDAC by modulating angiogenesis and mitigating the inflammatory response.

Exosomes derived from antigen-presenting cells, such as dendritic cells and macrophages, play a pivotal role in transporting and presenting functional MHC peptide complexes to modulate antigen-specific T cell responses. This underscores their protective function in attenuating inflammation or enhancing immune responses (169). In the context of cancer vaccine development, computational structural modeling has been employed to predict immunogenic neoepitopes for cancer vaccines, with a specific focus on targeting neoantigens predicted using MHC binding algorithms (170).

Tumor cells typically require the production of angiogenic growth factors to establish their vascular network, among which cytokines such as vascular endothelial-derived growth factor (VEGF), and roundabout guidance receptor 1 (ROBO1) play crucial roles in the process of angiogenesis within PDAC (171–174). Lee et al (175) and Pakravan et al (176) reported that exosomes derived from mesenchymal stromal cells (MSCs) can selectively target tumor cells by utilizing miR-16 or miR-100, thereby modulating the mechanistic target of rapamycin/hypoxia inducible factor 1-alpha signaling pathway to suppress intracellular VEGF expression and consequently attenuate the angiogenic potential of tumor cells.

In addition to MSCs, exosomes derived from PDAC cells may also possess corresponding anti-angiogenic mechanisms. Research has demonstrated that miR-29b originating from PDAC cells can downregulate VEGF expression and diminish the migration rate and angiogenesis capability of vascular endothelial cells, primarily by suppressing ROBO1 and SLIT-ROBO Rho GTPase-activating protein 2, thereby attenuating the angiogenesis induced by PDAC cells (173).

The TME is a complex and diverse ecosystem comprising cancer cells, fibroblasts, adipocytes, endothelial cells and mesenchymal stem cells (177). The exosomes can also be derived from CAFs and other stromal cells within the TME (62). CAFs, a heterogeneous stromal cell population with diverse cellular origins, phenotypes and functions, represent one of the significant sources of exosomes within the TME (178,179). For example, CAFs can utilize the miR-135b5p/Forkhead box transcription factor O1 axis to promote the formation of new blood vessels for cancer cells (180). Additionally, CAFs have the ability to induce expression of lnc HOTAIR, which facilitates tumor metastasis by promoting EMT (181,182). Moreover, exosomes derived from CAFs enhance tumor drug resistance and self-renewal capabilities of cancer stem cells by providing them with mitochondrial genomes that improve oxidative phosphorylation and mitochondrial metabolism (183). These exosomes also contain essential metabolites such as amino acids, lipids and tricarboxylic acid cycle intermediates that are utilized by cancer cells during periods of nutritional deficiency or stress. Furthermore, CAFs contribute to tumor resistance against anticancer treatments through their secretion of multiple exosomes (184). For instance, these exosomes can activate retinoic acid inducible gene 1 protein signaling in cancer cells or stimulate NOTCH3 signaling on cancer cells via Jagged 1 present on CAFs. The collaboration between these pathways ultimately leads to enhanced resistance against radiation therapy and chemotherapy (185). By targeting the aforementioned mechanisms, pharmaceutical interventions can be developed for the treatment of PDAC.

Specialized adipocytes known as cancer-associated adipocytes (CAAs) play a significant role in various tumor types, including BRCA, ovarian cancer, PDAC, kidney, gastric and colon cancers (186). These CAAs interact with tumor cells, leading to alterations in their properties and functions. The impact of specific miRNAs, such as miR-144, miR-126 and miR-155, present in exosomes on tumor growth, has been observed to be mediated through their targeted influence on adipocytes (187). Moreover, in the presence of tumor cells, adipocytes upregulate exosomal miRNA-155 levels to attract macrophages and facilitate their differentiation into TAMs that support tumor growth (188–190). Additionally, CAA secretion of visfatin has been shown to induce M2 phenotype polarization in macrophages that promotes malignancy and enhances glycolysis.

The exosomes can also originate from normal fibroblast-like mesenchymal cells and bear distinct markers of PDAC tumor cells (191,192). Therefore, exosomes within the TME can originate from a diverse range of cellular sources, extending beyond MSCs and PDAC cells, including CAFs, CAA and tumor-associated endothelial cells (193). Exosomes from these sources have been shown to be related to cancer metabolism and drug resistance in pan-cancer studies, and it may be possible to diagnose PDAC cells drug resistance through them, but the specific mechanism has not been clearly studied (10,194).

The progression of PDAC is intricately linked to the migration, invasion and metastasis of PDAC cells (195). A disintegrin and metalloproteinase domain-containing 9 protein is a relevant protein implicated in the advancement, metastasis and unfavorable prognosis of tumors (196). Shang et al (197) discovered that miR-1231 was commonly employed as one of the diagnostic markers for early-stage PDAC progression in previous studies. However, their animal experiments revealed that MSC exosomes carrying miR-1231 exerted a negative regulatory effect on the migration, invasion and adhesion of PDAC cells, thereby effectively inhibiting PDAC activity (197). The study conducted by Yao et al (198) proposed that circular RNA present in mesenchymal stem cell exosomes may play a pivotal role in the progression of PDAC. Through comprehensive transcriptome gene sequencing and heat map analysis, circ-0030167 was found to specifically target the expression of WNT inhibitory factor-1 in PDAC cells by interacting with miR-338-5p, thereby effectively suppressing the aberrant activation of the Wnt signaling pathway. Consequently, this regulatory mechanism exerts inhibitory effects on both proliferation and migration processes in PDAC cells.

Once tumor cells develop drug resistance, the effectiveness of chemotherapy drugs will be significantly diminished. Preliminary experiments have indicated that the drug resistance in tumor cells is associated with the activation of calmodulin-dependent kinases/Raf/MEK/ERK signaling pathway, and in vivo exosomes derived from MSCs may play a crucial role in the mechanism underlying tumor cell dormancy (199–201). The findings of Ono et al (202) demonstrated that MSCs exosomes transferred miR-23b to tumor cells, thereby inducing tumor dormancy through the inhibition of MARCKS expression. These results are consistent with those reported by Yang et al (203). They suggested that in vivo, MSCs could induce tumor cell quiescence and enhance drug resistance through dormancy, highlighting the significance of exosomes as crucial targets for reducing tumor drug resistance. Expanding on this hypothesis, Fu et al (204 and Fan et al (205) conducted in vitro experiments to validate the substantial impact of exosome miR-520-5p and Ephrin type-A receptor 2 (EphA2) on GEM resistance and transfer of drug resistance in PDAC cells. However, ongoing exosome research focused on exosomes aimed at mitigating drug resistance in PDAC necessitates further elucidation of the influence of drug resistance and its generation mechanism.

The precise targeting capabilities of exosomes suggest potential for personalized treatment strategies in PDAC. For instance, an optimized approach to exploit variable biomarker expressions is being developed in PDAC using a specialized formulation of exosomes loaded with erastin, which selectively targets triple-negative BRCA cells by leveraging the overexpression of folate receptors (206,207).

Exosomes derived from cancer cells have been employed not only for efficient drug delivery but also as nanoanalytical contrast agents, particularly in the diagnosis and monitoring of PDAC. Comparative investigations conducted on other gastrointestinal malignancies reveal a significant underutilization of such diagnostic applications in gastric and colon cancers, where research predominantly focuses on fundamental cellular interactions and molecular cargo analysis (208).

Furthermore, the novel use of milk-derived exosomes for the oral delivery of hydrophobic drugs represents a significant breakthrough with potential applications in gastrointestinal cancer treatments (209). In PDAC, where invasive interventions are prevalent, the development of oral exosome-based therapies could profoundly transform treatment strategies by offering less invasive and more patient-centric alternatives.

While significant progress has been made in exosome research for PDAC, there is a pressing need for more extensive investigations into diagnostic and therapeutic applications in other gastrointestinal cancers. The distinct challenges posed by PDAC, characterized by its aggressive nature and often late-stage diagnosis, necessitate tailored approaches that may not be directly applicable to less aggressive or differently behaving tumors. Nevertheless, the fundamental principles derived from exosome research can inform broader strategies in gastrointestinal oncology, fostering interdisciplinary innovations and potentially identifying universal or cancer-specific therapeutic targets.

To enrich the discourse on the role of exosomes in the prognosis of PDAC, a comprehensive compilation about various exosomal markers and their associated biological processes is presented in Table II. For instance, exosomes derived from PC cells exhibit markers such as c-Met and PD-L1, which are implicated in promoting invasive expansion and immune evasion, thereby adversely affecting prognosis (210). Additionally, exosomes from malignant ascites of patients with PC, characterized by the presence of CD133 and other cancer stem cell markers, contribute to the establishment of a TME that facilitates tumor growth, metastasis and angiogenesis (211). These processes further induce immune suppression and drug resistance, ultimately impacting patient outcomes.

In the context of blood plasma, exosomal miR-451a has been identified as a significant independent factor for overall survival and disease-free survival in PDAC, regulating key biological processes such as proliferation, invasion and metastasis (212). Similarly, EphA2 found in serum exosomes correlates positively with tumor stage and reduced survival rates, highlighting its role in cancer cell proliferation and invasion (213).

Moreover, the upregulation of miR-23b-3p in serum exosomes from patients with PDAC promotes cell proliferation, migration and invasion, demonstrating its association with CA19-9 levels, a common tumor marker (214). The involvement of miR-3607-3p, enriched in exosomes from natural killer cells, suggests a potential prognostic marker, as low levels of this miRNA are linked to poor prognosis in PDAC (94).

Exosomal miR-222 has been shown to enhance cell proliferation and invasion by downregulating p27 through the miR-222/PPP2R2A/AKT pathway, indicating its relevance in PC incidence and prognosis (215). Additionally, miR-106b and miR-146a contribute to GEM resistance in cancer cells, with miR-146a promoting epithelial cell proliferation and survival upon transfer to recipient cells (216,217).

Finally, the long-term exposure of PDAC cells to GEM leads to the upregulation of miR-155, which promotes anti-apoptosis and exosome secretion, thereby facilitating chemoresistance. This miRNA is also transferred to other PDAC cells, inducing functional changes that may impact treatment outcomes (218). MiR-212-3p in PDAC exosomes has been shown to suppress immune responses by impairing CD4⁺ T cell activation, fostering an immunotolerant microenvironment (219). Furthermore, miR-501-3p, derived from M2 macrophage exosomes, inhibits transforming growth factor beta receptor 3, disrupting the TGF-β signaling pathway and promoting a pro-TME that facilitates PDAC development (220).

To help with a more comprehensive understanding, exosomal markers in the treatment of PDAC have also been summarized in Table III. Notably, exosomes derived from bone marrow mesenchymal stem cells have been shown to effectively deliver chemotherapeutic agents such as oxaliplatin and siRNA to tumors, thereby enhancing antitumor immunity and prolonging the circulation of therapeutic cargo (221). Furthermore, fibroblast-derived exosomes have been implicated in promoting PC cell survival through the release of mRNA and miRNA, with the inhibition of exosome secretion via GW4869 leading to a reversal of drug resistance and suppression of tumor growth (217).

Additionally, miR-1231 from bone marrow mesenchymal stem cells has demonstrated a suppressive impact on PC cell proliferation, migration, invasion and adhesion (197). Autologous exosomes secreted by PC cells have been utilized for targeted delivery of GEM, highlighting the potential of exosomes as vehicles for chemotherapeutic agents (222). The engineering of exosomes to deliver RNA specifically targeting oncogenic KRASG12D has also shown promise in achieving targeted inhibition of PC cells driven by this mutation (223).

Moreover, the combination of tumor-exosome-loaded dendritic cells with cytotoxic drugs has been reported to enhance T cell recovery and improve survival outcomes (224). Chlorin e6-loaded tumor-derived re-assembled exosomes have enabled the integration of photodynamic therapy and immune therapy, resulting in the generation of reactive oxygen species and enhanced cytokine release (225). Ongoing research into exosomal proteins from PANC-1 cells aims to assess their potential in activating dendritic cells and cytokine-induced killer cells, further exploring agonists for their activation (226). Finally, the application of exosomes in the treatment and diagnosis of PDAC was summarized, as depicted in Fig. 2.

The exosomes, serving as endogenous carriers of molecular information between cells, possess the characteristics of small size and excellent biocompatibility (227). Exosomes can serve as a versatile drug carrier capable of encapsulating diverse compounds, including small molecule chemical drugs, proteins and nucleic acids (228,229). The use of exosomes as drug carriers is advantageous due to their ability to preserve the biological activity of drugs within the membrane, while also avoiding any immune response in vivo. This renders them more suitable for delivery compared with traditional nano-delivery carriers such as liposomes, thus making it a prominent area of research in tumor therapy (230,231).

The low immunogenicity and high tissue permeability of exosomes confer significant advantages for the delivery of small molecule drugs, such as siRNA and miRNA. Previous studies have demonstrated that exosomes derived from 293 cells, when loaded with exogenous siRNA, can effectively inhibit tumor cell growth by silencing the human epidermal growth factor receptor 2 gene (232). The study conducted by Zuo et al (233) employed ultrasound for the transfection of miR-34a into exosomes. The findings demonstrated that ExomiR-34a effectively traversed the cell membrane and downregulated the expression of its target gene BCL-2, thereby inducing apoptosis in PDAC cells. Moreover, it significantly impeded tumor proliferation in vivo (233). The miRNA-145-5p functions as a potent tumor suppressor, exhibiting a significant correlation with the extent of macrophage infiltration. Ding et al (234) proposed that its dysregulation is closely associated with aberrant proliferation and invasion of PDAC cells. By constructing vectors for engineering MSC exosomes, exogenous miR-145-5p was utilized in animal experiments pertaining to the progression of PDAC. The findings demonstrated that exosomes containing miR-145-5p significantly impeded the in vivo growth of PDAC cells by inducing cell cycle arrest and augmenting the apoptosis rate of these cells.

Chemical drugs often induce a variety of allergic or complication reactions due to their low targeting efficacy (235). However, MSC exosomes possess inherent tumor-targeting properties derived from their parental cells, and the abundance of proteins on their membrane provides numerous targeting ligands and chemical modification sites for engineering exosomes specifically designed to target tumor cells (236). Therefore, exosomes derived from MSCs present a promising solution to overcome this challenge. Pascucci et al (237) conducted experiments to investigate the therapeutic effects of MSC exosomes loaded with PTX, which were generated through co-culture method. The results demonstrated that PTX-loaded exosomes exhibited a significant inhibitory effect on the proliferation activity of PDAC cells compared with PTX alone. Furthermore, in line with this hypothesis, several studies have also confirmed the efficacy of MSC exosomes loaded with GEM, a standard chemotherapy drug for PDAC. In vitro experiments have revealed a certain degree of growth inhibition in PDAC cells, and from a pharmacological perspective, local administration of MSC exosomes loaded with GEM can significantly enhance drug concentration. Consequently, it is possible to design a more effective targeting strategy for PDAC lesion areas (238). The effect of GEM-loaded MSCs exosomes on systemic toxicity and efficacy was validated by Li et al (222) through the establishment of a PDAC animal model (222). The results demonstrated that EXO-GEM induced minimal harm to mice compared with direct injection of GEM, while significantly suppressing tumor proliferation without any indications of tumor recurrence in mice. Considering the common clinical application of combined therapies involving GEM and PTX, Zhou et al (160) constructed MSCs exosomes loaded with both GEM and PTX for PDAC treatment. Compared with the chemo-drug group, the MSCs exosomes-chemo-drug group exhibited greater persistence and targeting, resulting in higher overall survival rates compared with other control groups.

It is noteworthy that the clearance of exosomes by pancreatic and immune cells can exert an influence on the TME and thereby impact the progression or inhibition of PDAC. This aspect holds particular significance in cases where exosomes are employed as drug delivery vehicles. Kamerkar et al (223) have reported that the presence of CD47 on exosomes hampers their clearance, rendering them more adept at evading phagocytic elimination compared with liposomes. This evasion mechanism is partly mediated by cluster of differentiation 47-signal-regulatory protein alpha interactions on exosomes, which aid in circumventing host immune surveillance signals known as ‘don't eat me’ signals (223). The presence of plasma membrane-like phospholipids and membrane-anchored proteins in exosomes may contribute to their reduced clearance from the circulation (239–241). Although CD47 does not play a significant role in facilitating the entry of exosomes into pancreatic cells, the enhanced macropinocytosis observed in KRAS-mutant cancer cells promotes their uptake of exosomes (242,243). Further investigation is warranted to explore whether exosomes can evade lysosome-dependent degradation of their cargo by utilizing macropinocytosis as an entry mechanism.

Moreover, comprehensive assessment of the in vivo efficacy and safety of these engineered exosomes involves a diverse range of techniques. These encompass nanoparticle tracking analysis for validating size uniformity and particle concentration, flow cytometry for confirming surface marker expression and ensuring accurate cellular sourcing, as well as in vivo assays for directly measuring therapeutic impact and safety profiles (244). Rigorous testing is essential to advance these platforms towards clinical applications.

Intriguingly, the conventional notion of the pancreas as a sterile environment has been recently challenged by suggesting the presence of bacteria capable of secreting exosomes (245). These bacterial exosomes have emerged as potential contributors to the dynamics of PDAC, exerting influence on tumor progression and drug resistance (246). Despite their significant implications, this microbial aspect remains understudied in relation to PDAC, highlighting a critical gap in current research. Exploring the intricate interplay between bacterial exosomes and pancreatic tumors opens up new avenues for comprehending the multifaceted nature of this malignancy.

From a clinical and anatomical perspective, there is no direct physical connection between the pancreas and the gut microbiota; therefore, the pancreas is considered to be a sterile tissue (247,248). However, microorganisms can migrate to the pancreas through the bile duct in the digestive tract (249,250). Numerous studies have demonstrated a robust correlation between the composition of oral, gastrointestinal, fecal and organ-specific (pancreatic) microbiota and PDAC (251). The development of periodontal disease in the oral cavity has been associated with several key pathogenic bacteria, including Porphyromonas gingivalis, Fusobacterium, Streptococcus mitis and Neisseria elongata (252). The secretion of peptidyl-arginine deiminase by Porphyromonas gingivalis is hypothesized to induce mutations in the KRAS and tumor suppressor p53 genes, thereby degrading arginine metabolism (253). The oral administration of fluorescently-labeled Enterococcus faecalis to wild type mice in an experiment resulted in the observation of fluorescence in the pancreas, indicating bacterial migration from the gastrointestinal tract to the pancreas (254). The ability of bacteria to transfer intracellular materials outside the body via exosomes suggests that targeting bacterial exosomes could be a potential therapeutic approach for treating PDAC (255).

The journey from laboratory discovery to clinical application is always challenging, and this holds true for PDAC-specific exosomes as well. In this arduous process, the initial crucial step involves isolating high-quality PDAC-specific exosomes. Recent advancements in microfluidic technologies have facilitated the efficient capture of exosomes from small blood volumes using highly specific antibodies (34). Although this method has the potential to enable early screening using simple fingertip samples from patients, there are significant challenges in scaling up the technology for clinical use due to its complexity, costliness and requirement for specialized equipment (34).

The second challenge lies in the safety of modified exosomes. Numerous modified exosomes have been utilized for targeted delivery of therapeutic agents such as small molecule drugs, nucleic acids and proteins to cancer cells. A comprehensive assessment of the ethical and legal implications associated with these innovative treatments is imperative to ensure patient safety under appropriate therapeutic conditions. For instance, early clinical trials have demonstrated the potential efficacy of mesenchymal stem cell-derived exosomes loaded with therapeutic siRNA targeting the mutant KRAS-G12D gene for treating metastatic PDAC. However, concerns exist regarding the inadvertent promotion of tumor growth and metastasis by these vesicles (34).

Moreover, there are certain limitations associated with engineering exosomes. Modifications inevitably affect the natural properties and delivery efficacy of exosomes, thus achieving a balance between harnessing their complete therapeutic potential while preserving inherent functionalities remains a key challenge. Additionally, production and purification processes require high efficiency and reproducibility to ensure a pure population of exosomes. However, conventional methods such as differential centrifugation often yield preparations contaminated with protein aggregates and other cellular debris (256). This highlights the necessity of developing advanced and scalable purification techniques that comply with clinical standards. Continuous innovation in exosome isolation and purification technologies, along with comprehensive clinical trials to evaluate the safety and efficacy of exosome-based interventions, is crucial for addressing these challenges and limitations.

In addition to PC, gastrointestinal cancers such as gastric, colorectal and liver cancers have also emerged as significant areas of interest in exosomal research. Numerous miRNAs, lncRNAs, circRNAs and proteins have been identified as potential diagnostic and prognostic biomarkers or therapeutic targets for gastroenterological malignancies (257–259). Due to its high global mortality rate, PC has garnered extensive attention from researchers aiming to develop diverse engineered exosomes that could facilitate the exploration of novel opportunities for generating clinical-grade exosomal technologies and drugs.

Therefore, it is imperative to overcome the challenges and limitations in order to fully exploit the potential of exosomes in PDAC diagnosis and treatment. This will facilitate more efficacious disease management and establish a precedent for broader application of exosomal therapies in the field of oncology.

PDAC is the most prevalent and lethal disease among solid malignant tumors. Conventional tumor drugs used for treatment often lead to drug resistance without any targeted alternatives available, resulting in a challenging situation for PDAC diagnosis and treatment. In addition to replacing existing biomarkers for PDAC diagnosis, exosomes can enhance the accuracy rate by combining detection methods or serving as an auxiliary tool alongside existing techniques such as endoscopy, ultrasound detection and imaging. Moreover, exosomes can differentiate between different stages of PDAC progression based on their content, potentially playing a broader role in clinical diagnosis and treatment. Additionally, due to their intercellular communication capabilities along with their safety profile and targeting abilities, exosomes hold potential as a novel therapeutic option. Their unique lipid structure also enables them to act as efficient drug delivery vehicles that prolong drug action time within the body while reducing toxicity levels when treating PDAC and other cancers. However, current diagnostic and therapeutic applications involving exosomes are still limited to preclinical experimental stages; thus, further comprehensive clinical research studies and trials are warranted. It is anticipated that exosomes will become an effective tool or method for precise diagnosis and treatment of PDAC in the future.