Dysregulation of the PI3K/Akt signalling pathway is characteristic of carcinogenesis, and activation of this signalling pathway enhances cancer cell proliferation, angiogenesis and resistance to chemotherapy and immunotherapy (33). PI3K can be activated by tyrosine kinases to produce phosphatidylinositol-3,4,5-trisphosphate (PIP3) in the plasma membrane. Phosphatase and tensin homolog (PTEN) is a tumour suppressor, and PIP3 is dephosphorylated by PTEN and reduced to PIP2, thus preventing the activation of Akt. If the inhibition of PTEN expression leads to Akt activation, it causes the activation of mTOR signalling and the inhibition of pro-apoptotic gene expression, which promotes tumour growth and proliferation and inhibits apoptosis (34).

By targeting PTEN and activating the PI3K/Akt signalling pathway, miRNA-21 can lead to uncontrolled proliferation of tumour cells and promote tumour cell migration, metastasis, inhibition of apoptosis and drug resistance (35). This approach can make the treatment of lung cancer more challenging. Inhibitors of miRNA-21 can inhibit PI3K/Akt and thus prevent metastasis and invasion, and promote apoptosis in lung cancer. The underlying mechanism involves miRNA-21 targeting the apoptosis-stimulating protein 2 of p53 (ASPP2) (36). The inhibition of miRNA-21 expression can inhibit PI3K/Akt signaling and thus make lung cancer cells more sensitive to radiotherapy (37). Additionally, the lncRNA CASC2, in combination with miRNA-21, can increase PTEN expression, inhibit the PI3K/Akt signalling pathway and promote cisplatin-induced apoptosis in lung cancer cells (38). Overall, miRNA-21 can activate the PI3K/Akt pathway to promote lung cancer progression.

The MEK/ERK signalling pathway is a classical MAPK signalling pathway that involves the classical Ras/Raf/MEK/ERK pathway with Ras/Raf proteins and the activation of ERK upon phosphorylation of MEK, which is involved in mitotic signalling and regulates cell proliferation, differentiation, migration, apoptosis and drug resistance (39). Upregulation of MEK/ERK can lead to the progression of different types of cancers (40). Researchers have also investigated the targeting of other components of the MEK/ERK signalling pathway for therapeutic intervention. Examples include targeting upstream EGFR family members and the RAF/MEK/ERK pathway regulators Src homologous protein tyrosine phosphatase 2 and son of sevenless homolog 1 (41).

Trametinib is a Food and Drug Administration (FDA)-approved ERK inhibitor and is also approved in combination with dabrafenib for treating patients with BRAF V600E-mutated NSCLC (42). Trametinib inhibits miRNA-21 expression, promotes the expression of the downstream target gene programmed cell death factor 4 (PDCD4), downregulates MEK1/2 and ERK1/2 expression, inhibits the MEK/ERK pathway and restores the sensitivity of ositinib-resistant NSCLC cells to ositinib (43).

The cytokine TGF-β has three isoforms: TGF-β1, TGF-β2 and TGF-β3. SMAD is an intracellular protein and downstream target of TGF-β that transduces extracellular signals from cell surface receptors and participates in the regulation of cellular processes such as proliferation, motility and differentiation (44). The SMAD family has eight members, which include receptor activated Smad1, 2, 3, 5 and 8, comediator Smad 4, and inhibitory SMAD6 and SMAD7. Inhibitory SMAD7 can negatively regulate the TGF-β/SMAD signalling pathway via feedback, which in turn blocks the biological effects of TGF-β (45).

Activation of the TGF-β/SMAD signalling pathway often promotes angiogenesis and triggers epithelial-to-mesenchymal transition (EMT), which leads to a loss of polarity and adhesion properties of cells, thereby promoting cell invasion and metastasis (46). Studies have reported that miRNA-21 can activate the TGF-β/SMAD signalling pathway by inhibiting the expression of SMAD7, leading to the upregulation of the expression of the mesenchymal markers Nanog, CD44, Sox2 and Snail, triggering EMT, which allows human bronchial cells to acquire tumour-initiating stem cell-like features, which in turn promotes transformation into a lung tumor-like phenotype (45).

The group members of the Hippo signaling pathway include transcriptional coactivators containing PDZ-binding motifs (TAZ), large tumor suppressor genes 1/2 (LATS1/2), mammalian sterile lineage 20-like kinase 1/2 and Yes-associated proteins (YAP). Among them, activating YAP/TAZ phosphorylation plays a major role in various functions of the Hippo/YAP signalling pathway. When the Hippo signalling pathway is activated, YAP and TAZ are phosphorylated by LATS1/2 and then restricted to the cytoplasm and degraded by 14-3-3 proteins; these changes inhibit the oncogenic effects of YAP/TAZ. However, when the Hippo signalling pathway is inhibited, unphosphorylated YAP/TAZ is transferred to the nucleus and binds to the TEA structural domains 1-4 to regulate the transcription of relevant target genes, thus exerting a cancer-promoting effect. In NSCLC, activation of the Hippo signalling pathway and a reduction in YAP phosphorylation can inhibit the proliferation and migration of NSCLC cells (47). Notably, miRNA-21 can target kidney and brain expressed protein to inhibit the Hippo signalling pathway and promote lung cancer proliferation, invasion and metastasis (48).

The protein complex NF-κB is an important regulator of cellular inflammation, metabolism, immunity and cell survival (49). It contains dimeric proteins formed by two subunits, p50 and p65. Normally, NF-κB is bound to its inhibitor IκB and is enclosed in the cytoplasm. When stimulated by intracellular and extracellular stimuli, IκB kinase is activated, leading to phosphorylation and degradation of IκB, which promotes the release of NF-κB and its entry into the nucleus to play a gene-regulatory role and participate in the induction of inflammation, cell proliferation, and apoptosis (50). In cancer, NF-κB is abnormally activated, leading to a sustained inflammatory response, promotion of angiogenesis and immune evasion, creating a sustained favourable tumor microenvironment for tumour cells (51).

Notably, miRNA-21 can activate the NF-κB pathway by targeting negative regulators of the NF-κB pathway, thereby activating the NF-κB pathway. For instance, miRNA-21 targets PTEN, activates the NF-κB pathway, promotes the expression of the proinflammatory factors interleukin (IL)-6 and IL-8, and inhibits the expression of cleaved caspase-3, which provides lung cancer cells with a sustained inflammatory microenvironment and inhibits apoptosis (52). Studies have shown that miRNA-21 can target PTEN, promote NF-κB and promote cisplatin resistance in lung cancer cells (53). Thus, miRNA-21 can promote lung cancer progression by activating the NF-κB pathway.

STAT3 is a member of the STAT family of proteins that are implicated in physiological processes such as cell proliferation, differentiation, apoptosis and angiogenesis. The Janus protein tyrosine kinase (JAK)/STAT signalling pathway mediates STAT3 activation (54). The JAK/STAT signalling pathway comprises mainly the JAK family, STAT and receptor tyrosine kinases. The JAK family contains JAK1, JAK2, JAK3 and selective tyrosine kinase 2, which binds noncovalently to cytokine receptors, triggering the phosphorylation of resting STAT monomers in the cytoplasm and leading to homodimerization or heterodimerisation of STAT. The altered STAT translocates to the nucleus and acts as a transcription factor to regulate gene transcription, which is associated with cell differentiation, proliferation and apoptosis (55). Src-homology domain 2-containing protein tyrosine phosphatase 1 (SHP-1), SHP-2 and suppressor of cytokine signal transduction (SOCS) family proteins are negative regulators of the JAK/STAT signalling pathway. In cancer, miRNA-21 can activate the JAK/STAT pathway by downregulating the expression of SOCS1 (56). Additionally, miRNA-21 targets PDCD4, downregulates SHP-1 expression and activates STAT3 expression, which in turn helps arsenic induce bronchial epithelial cells to undergo malignant transformation and acquire cancer stem cell stemness (57).

The cell cycle leads to cell proliferation, allowing cells to grow, replicate genetic material and divide. The cell cycle has four main phases: Gap 1 (G1), DNA replication (S), G2 and mitosis (M). Alterations in the mechanisms of the cell cycle constitute one of the main pathways by which normal cell proliferation is transformed into uncontrolled cell division and, ultimately, carcinogenesis and cancer progression (70). Cell cycle proteins and cyclin-dependent kinases (CDK) are key regulators that influence the progression of the cell cycle (71). Targeting key regulators of the cell cycle in cancer is an effective approach to treat tumors. Overexpression of miRNA-21 increases the expression of the cell cycle protein D1 and the cell cycle protein E1, which in turn promotes the proliferation of lung cancer cells (72). Xia et al (73) reported that the expression of anti-miRNA-21 significantly decreased the expression of cell division cycle 2 and cell cycle protein B1 in lung cancer, which in turn increased the number of cells in G2/M phase and decreased the number of cells in S phase. Zhong et al (74) reported that downregulation of miRNA-21 expression resulted in arrest of lung cancer cells in G2/M phase, which inhibited cell proliferation. By contrast, overexpression of miRNA-21 increased the number of tumor cells in S-phase, which promoted cell proliferation. The underlying mechanism was related to the fact that miRNA-21 can target human mutS homolog 2 (74). Similarly, Li et al (61) found that the expression of miRNA-21 increased considerably after plasmid transfection, leading to a decrease in the G2-phase population of cells and an increase in the S-phase population. These changes imply that the lung cancer cells were still undergoing DNA replication and cell proliferation (61). Jin and Yu (60) reported that Hypoxic lung cancer cell-derived exosomal miRNA-21 can mediates macrophage M2 polarization and promotes lung cancer cell proliferation by target interferon-regulatory factors 1. Circ_0001287 can upregulate PTEN expression by sponging miRNA-21, which in turn inhibits the proliferation of lung cancer cells, whereas overexpression of miRNA-21 reversed this process (64). These studies indicate that increasing the expression of miRNA-21 promotes the proliferation of lung cancer cells.

Lung cancer is a highly malignant and lethal cancer associated with cell invasion and metastasis. Metastasis of tumour cells to distant sites leads to severe organ failure at secondary sites, where epithelial-mesenchymal transition (EMT) is an important route to promote the invasion and metastasis of lung cancer (75). The occurrence of EMT causes the cells to change from a non-motile epithelial state to a motile mesenchymal state, which increases the malignant characteristics of the tumour cells. Among them, the expression of epithelial marker E-cadherin decreases, whereas the expression of mesenchymal markers such as N-cadherin and waveform protein increases (76). Additionally, tumor cell invasion and metastasis are also associated with an increase in the expression of matrix metalloproteinase (MMP), which promotes tumor cell invasion and metastasis by facilitating the degradation of the extracellular matrix (77). Sinomenine downregulates miRNA-21 expression, which in turn increases E-cadherin expression, reversing the induction of cysteine-rich protein with kazal motifs (RECK), tissue inhibitor of metalloproteinase 1 (TIMP1) and TIMP2 expression, inhibits the expression of MMP2, MMP9, waveform protein and CD147 (which can activate MMP proteins), and thus reduces the invasive ability of lung cancer cells. The underlying mechanism is related to the targeting of the downstream target gene RECK by miRNA-21 (78). RECK can negatively regulate EMT and the MMP and reduce the invasion and metastasis of cancer (79). Lung cancer tumor spheroids are enriched with miRNA-21, which can promote macrophage polarisation and EMT, accelerate ERK/STAT3 signalling and thus promote lung cancer cell metastasis to the brain (80). Xia et al (66) found that the lncRNA PLAC2 can act as a sponge for miRNA-21 and downregulate the expression of miRNA-21 to promote PTEN expression, which in turn inhibits the migration and invasion of lung cancer cells, whereas overexpression of miRNA-21 can reverse the inhibitory effect of the lncRNA PLAC2 on lung cancer cells. The combined effect of downregulation of miRNA-21 expression and upregulation of let-7 (one of the two earliest discovered miRNA) was superior to single regulation in inhibiting the invasion and migration of lung cancer cells. The combined effect of the two is also a direction of research on cancer treatment in the future (81). These studies suggest that high expression of miRNA-21 promotes metastasis and invasion of lung cancer.

Apoptosis is the main form of programmed cell death. In cancer, cell-autonomous apoptosis constitutes a common tumor suppressor mechanism, and the induction of apoptosis in tumor cells is the primary method of cancer treatment (82). Apoptosis is mainly mediated by the death receptor-mediated extrinsic pathway, the mitochondria-mediated intrinsic pathway and the endoplasmic reticulum stress-mediated apoptotic pathway, which are mainly mediated by the B-cell lymphoma 2 (Bcl-2) family, the cysteinyl aspartate specific proteinase (Caspase) family, the Fas ligand and Fas receptor, and the tumor necrosis factor (TNF) receptor and TNF ligand binding, which are involved in the apoptotic process of the above pathway (83). Wu et al (29) reported that the lncRNA CASC2 promoted p53 protein and Bcl-2 associated X protein (Bax) expression and inhibited Bcl-2 expression by binding to miRNA-21, which in turn promoted apoptosis in lung cancer cells, and overexpression of miRNA-21 reversed this process. A similar study showed that direct inhibition of miRNA-21 expression in lung cancer cells promotes Bax expression and inhibits Bcl-2 expression, which in turn induces apoptosis (81). Ge et al (84) developed an antisense oligonucleotide drug that targets and inhibits the expression of miRNA-21 and subsequently promotes the expression of caspase-3 and caspase-8, which in turn promotes apoptosis in lung cancer cells. This, in turn, promoted apoptosis in lung cancer cells. Zhou et al (36) reported that miRNA-21 inhibitors can inhibit the PI3K/Akt/NF-κB signalling pathway, which promoted the expression of caspase-3, caspase-8 and caspase-9 and induced apoptosis in lung cancer cells, and the mechanism was related to the targeting of miRNA-21 to ASPP2. To summarize, downregulating miRNA-21 expression can promote apoptosis in lung cancer cells.

Malignant cells require nutrients to survive and proliferate. Rapidly growing tumors are heavily vascularised, whereas dormant tumours are not. Hence, tumor angiogenesis needs to be initiated for tumor progression (85). Vascular endothelial-derived growth factor (VEGF) is a key angiogenic factor in tumors and is involved in the initial stages of tumor development, progression and metastasis. Therefore, VEGF and its receptor-mediated signaling pathways have become important therapeutic targets for the treatment of various cancers (85). Liu et al (86) found that knocking down STAT3 in human bronchial epithelial cells inhibited the expression of miRNA-21, and inhibiting miRNA-21 expression reduced VEGF levels, which in turn inhibited angiogenesis and the malignant transformation of human bronchial epithelial cells. Zhao et al (87) reported that during the transformation of human bronchial epithelial cells into tumor cells induced by arsenite (a carcinogen), miRNA-21 and VEGF expression are elevated; however, downregulation of miRNA-21 expression suppressed the expression of VEGF, suggesting that arsenite exerts a protumor angiogenic effect through miRNA-21 expression. Dong et al (88) noted that the lung cancer cells in the miRNA-21-inhibited group rarely formed tubes and had shorter tube lengths and fewer junctions; however, the lung cancer cells in the negative control and mock groups had dense and uniform lumens, suggesting that miRNA-21 is closely associated with promoting angiogenesis in lung cancer.

Certain patients with lung cancer are diagnosed in the middle-to-late stage or after metastasis has occurred, as the disease remains inconspicuous for a long time. After such a late diagnosis, the opportunity for surgery is lost and conservative treatment becomes the main treatment method, involving chemotherapy, radiotherapy and targeted therapy (89). However, the five-year survival rate of patients receiving conservative treatment is <20% (5). The underlying reasons for these poor prognostic outcomes are related to drug resistance, increased adverse effects and poor response to radiotherapy. Certain studies found that miRNA-21 was associated with resistance to chemotherapy, radiotherapy and targeted therapy in lung cancer cells (38,90-93). The roles of miRNA-21 in the chemotherapy, radiotherapy and targeted therapy of lung cancer are presented in Table II.

The IC₅₀ values of carboplatin and paclitaxel were lower in A549 cells with miRNA-21 knockdown than in lung cancer A549 cells without miRNA-21 knockdown. This suggested that knockdown of miRNA-21 expression promotes the sensitivity of lung cancer cells to carboplatin and paclitaxel (59). Extracellular vesicles are nanoscale vesicles that can be used to deliver miRNA. Extracellular vesicles in lung cancer metastatic soft brain membranes can deliver miRNA-21 to lung cancer cells and are highly expressed, with suppressed expression of PTEN and PDCD4 but increased phosphorylated Akt protein levels. This, in turn, promotes methotrexate resistance in leptomeningeal metastasis lung cancer cells (90). Additionally, the lncRNA CASC2 binds to miRNA-21 and miRNA-18, promotes PTEN expression and inhibits the PTEN/PI3K/Akt pathway, which in turn increases the sensitivity of NSCLC to cisplatin (38). Liang et al (63) reported that the lncRNA ASBEL and the lncRNA Erbb4-IR can promote the expression of leucine zipper transcription factor-like 1, a downstream target gene of miRNA-21, and increase the sensitivity of lung cancer cells to gemcitabine and cisplatin, whereas the chemosensitivity-promoting effects of the lncRNA ASBEL and the lncRNA Erbb4-IR were attenuated when cells were transfected with miRNA-21 mimics. Perftoran (perfluorodecalin), an artificial oxygen carrier, can attenuate the hypoxia resistance of lung cancer cells to carboplatin by inhibiting miRNA-21 expression (94). Thus, miRNA-21 can reduce the sensitivity of lung cancer cells to chemotherapeutic drugs through multiple pathways. The combination of miRNA-21 with chemotherapeutic drugs may be a way to improve the efficacy of chemotherapy for treating lung cancer in the future.

Overexpression of miRNA-21 in lung cancer cells inhibits sensitivity of radiotherapy. For instance, the lncRNA growth arrest-specific transcript 5 can act as a sponge for miRNA-21 and inhibit its expression, promoting PTEN expression and inhibiting Akt phosphorylation, which in turn promotes the radiosensitivity of lung cancer cells (91). Zhang et al (92) designed ribonuclease-targeting chimeras that could degrade miRNA-21, and the degradation of miRNA-21 increased the expression of PDCD4, which in turn improved the sensitivity of lung cancer cells to radiation therapy. It has also been reported that circ_0001287 sponges miRNA-21, increases PTEN expression and promotes the radiosensitivity of lung cancer cells (64). In addition, miRNA-21 can promote glycolysis in NSCLC by upregulating the expression of hypoxia-inducible factor 1α, which in turn promotes radioresistance in NSCLC cells (95). These studies illustrate that overexpression of miRNA-21 promotes radioresistance in lung cancer cells. Inhibiting miRNA-21 expression in lung cancer cells may be an effective method to reverse resistance to radioresistance.

Targeted therapy is an important treatment option for patients with advanced lung cancer. EGFR-tyrosine kinase inhibitors (TKIs) are the most widely used targeted drugs for treating lung cancer and can improve patient survival, but resistance to these drugs decreases efficacy and may lead to cancer progression (96). It has been shown that miRNA-21 increased purine metabolism by targeting adenylosuccinate lyase, leading to persistent resistance to oxitinib in lung cancer cells (93). Gefitinib is an EGFR-TKI and miRNA-21 promotes phosphorylation and activation of Akt, facilitating resistance to gefitinib in lung cancer cells (97).

With the advancement in technology, the determination of miRNA-21 has become more precise and sensitive (98,99). Studies have found that miRNA-21 can also be used as a biomarker for lung cancer diagnosis, prognosis and response to treatment. Pang et al (100) revealed that miRNA-21 was highly expressed in the serum of patients with lung cancer and that miRNA-21 can be used as a diagnostic marker for lung cancer, with an area under the curve (AUC) value of 0.901. Based on TNM staging, miRNA-21 expression in patients with stage III and IV lung cancer was significantly higher than that in patients with stage I and II disease. The expression of miRNA-21 in patients with metastasis was significantly higher than that in patients without metastasis. These findings suggest that miRNA-21 can be used as a diagnostic biomarker for lung cancer diagnosis and pathological staging (100). The expression of peripheral blood miRNA-21 and miRNA-486 was highly accurate for early cancer in lung nodules, with an AUC value of 0.855 (101). This can help in the early diagnosis of lung cancer. Liu et al (102) reported that the expression level of exosomal miRNA-21 can distinguish between patients with lung cancer and healthy individuals.

One study reported that plasma miRNA-21 expression was significantly elevated in patients with NSCLC and that high miRNA-21 expression was positively correlated with lung cancer tumour size (103). Another study revealed that extracellular vesicular miRNA-21 expression in lung cancer pleural lavage fluid was correlated with lung cancer pleural infiltration and that miRNA-21 induced peritoneal cavity mesothelial mesenchymal transition, leading to cancer spread (104). High expression of miRNA-21 was associated with poor prognosis in patients with soft meningeal metastases of lung cancer, and miRNA-21 expression was negatively associated with OS in patients with soft meningeal metastases of lung cancer (90). Xu and Shi (105) found an increase in the expression of miRNA-21 in the serum of patients with NSCLC by conducting PCR. Another study revealed that miRNA-21 expression was significantly upregulated in 112 patients with NSCLC recurrence or metastasis (experimental group) compared to 68 control patients with newly diagnosed NSCLC. After a follow-up time of three years, the mortality rate of the experimental group was found to be 91.96%, while the mortality rate of the control group was only 57.35% (105). These findings suggested that miRNA-21 is associated with poor prognosis in patients with NSCLC.

Zhu et al (106) reported that the overall effective rate of treating patients with lung cancer brain metastases via whole-brain radiotherapy combined with intensity-modulated radiotherapy was 86% and the miRNA-21 expression level of the treated patients with lung cancer brain metastases was significantly lower. A low level of miRNA-21 was associated with prolonged OS in treated patients with lung cancer brain metastases and low miRNA-21 expression levels in treated patients were associated with carcinoembryonic antigen, neuron-specific enolase, squamous cell carcinoma antigen and other tumor marker expression levels (106). These findings suggest that the expression level of miRNA-21 can predict the efficacy of whole-brain radiotherapy combined with intensity-modulated radiotherapy (106).

As mentioned earlier, miRNA can be classified into two types: Tumor suppressors and oncogenes. The use of miRNA mimics or inhibitors and techniques to knock down miRNA expression may be an effective therapeutic strategy for treating cancer. In addition, the combination of miRNA mimics or inhibitors with chemotherapy, radiotherapy and targeted therapy can improve therapeutic sensitivity and benefit patients. Furthermore, miRNA-21 is an oncogene and inhibiting the expression of miRNA-21 has therapeutic potential for cancer treatment. CRISPR/Cas9 gene editing technology can identify activated oncogenes, inhibit proliferation and suppress growth in cancer cells by knocking out oncogenes (107). These effects subsequently reduced the proliferation, migration and colony formation of lung cancer cells and improve their sensitivity to carboplatin and paclitaxel (59). Certain cancer therapeutic agents, such as Tanshinone IIA and cryptotanshinone, inhibit the expression of miRNA-21, which in turn inhibits the proliferation and invasion of lung cancer cells via a mechanism related to the downregulation of miRNA-21, which promotes the expression of tight junction proteins (108). Downregulation of miRNA-21 combined with upregulation of let-7 had a stronger inhibitory effect on lung cancer than downregulation of miRNA-21 expression alone (81). These findings provide a new idea for future regulation of the expression of both miRNAs for lung cancer treatment. In addition, miRNA-21 plays a role in promoting therapeutic resistance to various chemotherapeutic agents, targeted drugs and radiotherapy, and the use of miRNA-21 inhibitors in combination with these approaches can increase treatment efficacy.

Strategies to inhibit miRNA-21 in lung cancer also include anti-miRNA-21 oligonucleotides (95), small molecules (109), miRNA sponges (110) and anti-miRNA-21 nanoparticle delivery strategies. Zhang et al (92) used an acidic pH/H₂O₂-activated ribonuclease-targeted chimera that could precisely degrade miRNA-21 expression in lung cancer cells, whereas other control miRNAs were not degraded; the degradation of miRNA-21 promoted PDCD4 expression, thereby increasing the sensitivity of lung cancer cells to radiotherapy and inhibiting tumour growth. Small-molecule inhibitors can induce specific changes in the structure and kinetics of pre-miR-21 by binding to pre-miR-21 and affecting the Dicer enzyme cleavage site, which in turn reduces miRNA-21 expression (109). Numerous lncRNAs, such as the lncRNA ASBEL and the lncRNA Erbb4-IR, can act as sponges for miRNA-21 and inhibit its expression, thereby preventing the progression of lung cancer (63).

A study reported that when QTsome lipid nanoparticles encapsulated with anti-miRNA-21 (QTPlus-AM21) were delivered to lung cancer cells, miRNA-21 expression was strongly inhibited, followed by significant inhibition of lung cancer cell growth in vitro (69). This study also revealed that QTPlus-AM21 promoted the sensitivity of lung cancer cells to erlotinib via a mechanism in which QTPlus-AM21 promoted PTEN expression and inhibited EGFR expression (69). Of note, the delivery of miRNA-21 inhibitors and adriamycin via a calcium phosphate-polymer nanoparticle system caused greater cytotoxicity and promoted the expression of the tumor suppressor PTEN in lung cancer cells compared to that recorded after using adriamycin alone (111). Additionally, co-delivery of anti-miRNA-21 and anti-miRNA-95 by calcium phosphate nanoparticles significantly inhibited lung cancer cell growth and promoted radiation sensitivity (112).