Role of interleukin‑32 in cancer biology (Review)
- Authors:
- Published online on: May 7, 2018 https://doi.org/10.3892/ol.2018.8649
- Pages: 41-47
Abstract
Introduction
Inflammation serves a pivotal role in carcinogenesis and the promotion, malignant conversion and migration of malignant tumours (1). It has been established that inflammatory conditions in certain organs increase the risk of cancer. Tumour-associated inflammation also enables cancer cells to escape from the surveillance of adaptive immunity and diminishes the cellular response to chemotherapeutic drugs (2). Therefore, inflammation is considered a hallmark of cancer (2,3). Studies have revealed the molecular and cellular pathways that are vital for linking inflammation and cancer (1). The effect of immune cells on tumour cells partly depends on the production of cytokines, chemokines, growth factors and reactive oxygen species. Pro- and anti-tumorigenic effects are exerted by tumour-associated cytokines; interleukin (IL)-1, IL-6 and IL-8 have been revealed to promote carcinogenesis and tumour growth and invasion (4–6). By contrast, IL-10 and IL-27 induce apoptosis in cancer cells and prevent the development of cancer (7,8). The pro-inflammatory cytokine IL-32 has also been implicated in the development of various types of cancer, including hepatocellular carcinoma, pancreatic cancer, oesophageal cancer, lung cancer, gastric cancer, colon cancer, breast cancer and cutaneous T-cell lymphoma (9–16).
IL-32 was first identified as natural killer cell transcript 4 (NK4) as it was detected in activated natural killer cells and T cells (17). The biological function of IL-32 remained unknown until 2005 when Kim et al (18) demonstrated for the first time that recombinant NK4 could induce several pro-inflammatory cytokines, including tumour necrosis factor (TNF)-α and IL-8 (18). IL-32 is located at human chromosome 16p13.3 and contains eight small exons. According to the GenBank Database, IL-32 has more than nine isoforms, which are transformed into four major splice variants: IL-32α, IL-32β, IL-32γ and IL-32δ (19). Among the variants, IL-32β appears the most abundant and IL32γ is the most broadly studied (20,21). Furthermore, IL-32γ can be spliced into IL-32β in vitro and in vivo. The overexpression of splice-resistant IL-32γ in THP1 cells or rheumatoid arthritis (RA) synovial fibroblasts revealed a greater induction of IL-6 and C-X-C motif chemokine ligand 8 than in the same models overexpressing IL-32β (22). In addition to inducing cytokine production, the transient overexpression of endogenous IL-32β or IL-32γ resulted in cell death, whereas IL-32α overexpression failed to induce cell death (23). Notably, restoring the IL-8 survival-signalling pathway by co-overexpressing C-X-C motif chemokine receptor 1 with IL-32β or IL-32γ in 293 cells prevented IL-32β but not IL-32γ from inducing cell death (23). These studies indicated functional differences between these diverse splice variants. The biological properties of each isoform have been described in several reports (24–26). IL-32α increases IL-6 expression in THP-1 promonocytic cells (27). This result was also supported by a report that revealed that IL-32α induced IL-6 production by inhibiting B-cell lymphoma 6 (28). However, IL-32θ-expressing THP-1 cells revealed a reduced expression of C-C motif chemokine ligand 5 (29). These studies suggested that IL-32 functions as an intracellular mediator of inflammation. Additionally, numerous studies have provided evidence that IL-32 has diverse functions due to the intracellular interactions of its isoforms (26,30).
IL-32γ, originally known as NK4, was anticipated to be a secreted protein because it contains a signal peptide sequence and lacks a transmembrane region (18). Kim et al (18) demonstrated that induced the overexpression of either IL-32α or IL-32β resulted in the secretion of their proteins and stimulated peripheral blood mononuclear cells (PBMCs), NK cells and A549 cells to release IL-32. Another study revealed that IL-32 was secreted from T cells undergoing apoptosis (20). By contrast, Heinhuis et al (22) reported that the overexpression of spliced or splice-resistant IL-32γ led to the secretion of IL-32 but did not result in the release of intracellular lactate dehydrogenase (22). Taken together, these results suggested that endogenous IL-32 can be secreted via non-classical and classical secretory pathways (31). A definitive receptor has not been discovered for IL-32, but proteinase 3 has been recently recognized as a specific IL-32 binding protein (32). Furthermore, IL-32 can bind the extracellular domain of integrins, which might act as receptors through the focal adhesion kinase 1 (FAK-1) signalling pathway (33). As an extracellular protein, IL-32 has been revealed to serve a crucial role in the process of monocyte differentiation into macrophage-like cells with phagocytic capacities (34). More recently, IL-32 was reported to promote monocyte differentiation into CD1c+ dendritic cells and CD163+CD68+ macrophages (35). Therefore, IL-32 not only induces the production of pro-inflammatory cytokines but also directly affects the development and maturation of specific immune cells. IL-32 is also involved in numerous inflammatory and infectious diseases, including rheumatoid arthritis, chronic obstructive pulmonary disease, mycobacterium tuberculosis infections and inflammatory bowel disease (36–39).
IL-32 expression in cancer
A number of studies on a diverse range of tumour types have investigated the clinical significance of IL-32 expression as a prognostic factor. A higher expression of IL-32 in cancerous tissues of the human liver, pancreas, oesophagus, lung and stomach has been revealed in comparison with the expression in normal tissue or serum (Table I) (9–11,13,40). The expression of IL-32α was upregulated in tissues and serum from patients with hepatocellular carcinoma (HCC) (9). Additionally, surgical tissues from patients with pancreatic cancer revealed significantly higher expression levels of IL-32 compared with that of healthy pancreatic or normal tissues (10). Immunohistochemical studies of oesophageal cancer tissues have revealed that oesophageal cancer cells stain positively for IL-32, whereas normal oesophageal cells display minimal staining (11). In human lung cancer, Sorrentino and Sorrentino et al (40) reported that high IL-32 expression was present in adenocarcinoma (AC), large-cell carcinoma and small cell lung cancer but not in squamous-cell carcinoma (SCC). Notably, in the present study, IL-32 expression was associated with a poor clinical outcome. These results are in line with those of a study that revealed that IL-32 is associated with tumour cell invasion and metastasis in primary lung adenocarcinoma (12). Furthermore, the positive correlation between IL-32 and cancer invasion that was demonstrated in lung cancer was also reported in gastric and breast cancer (13,15). Tsai et al (13) demonstrated that the overexpression of IL-32 in gastric cancer appeared to correlate with the aggressiveness of cancer and a poor prognosis. In a study that involved breast cancer, a positive link was demonstrated between IL-32 expression and tumour size, the number of lymph node metastases and tumour stage (15). However, there remains controversy regarding the expression and action of IL-32 in tumours. A recent report noted that, although cervical cancer tissues expressed a higher level of IL-32, the expression of IL-32 was not correlated with patient mortality (41). In chronic myelomonocytic leukaemia, IL-32 expression was lower than in healthy donors. Furthermore, IL-32 expression in stromal cells from the bone marrow of patients with leukaemia served an important role in inducing apoptosis in leukaemia cells (42).
In these studies, IL-32 served either an oncogenic or a tumour suppressive role, likely due to disparities in the predominant IL-32 isoform expressed in the tumour tissue. Genetic variations among different ethnic groups and the different clinical stages of tumours may also contribute to these contradictory results. The expression of IL-32 may be a valuable independent prognostic tumour marker for overall survival rates and the degree of metastasis in patients with various forms of cancer.
The role of IL-32 in cancer
The mitogenic properties of IL-32
IL-32 has been demonstrated to be involved in cancer development. A recent report noted that IL-32 can act as an important growth factor for human cutaneous T-cell lymphoma (CTCL) cells (16). The study revealed that IL-32 accelerated the proliferation of CTCL cell lines in a dose-dependent manner. Furthermore, the exposure of certain CTCL cell lines to anti-IL-32 antibodies in culture inhibited cell proliferation. These results indicated that IL-32 may be involved in the pathogenesis of CTCL as an autocrine growth factor. Similarly, extracellular IL-32 has also been proposed to act as a mitogenic factor in breast cancer (43). Our group recently revealed that IL-32 promoted multiple myeloma cell growth through inducing the production of IL-6 in bone marrow stromal cells (44). Intracellular IL-32 also affects tumour growth. In hepatocellular carcinoma cells transfected with IL-32 small interfering RNA (siRNA), intrinsic apoptosis was increased and cell growth was decreased compared with the level of these activities in the control siRNA-transfected cells (9). These results are consistent with those of one previous study demonstrating that IL-32 suppression abated anti-apoptotic protein expression in pancreatic cancer cells (10).
Contrary to the oncogenic role of IL-32 in cancer cell proliferation and death, a number of reports have demonstrated that IL-32 inhibits the proliferation of several types of cancer, including colon cancer, prostate cancer and melanoma (45,46). Induction of IL-32 expression inhibited the growth of colon cancer cells, while suppression of endogenous IL-32 was reported to reverse this inhibitory effect. This observation was also reproduced in prostate cancer and melanoma cells (45,46).
In addition to its role in tumour proliferation, IL-32 has also been linked to antitumour activities that are dependent on the influence of other cytokines and immune cells. Chronic myeloid leukaemia cell lines that overexpressed IL-32, upregulated the expression of Fas and UL16-binding protein 2 (47). In accordance with the results of the present study, Park et al (48) indicated that enforced overexpression of IL-32 in colon cancer cells potentiated the inhibitory effect of TNF-α and promoted the apoptosis of colon cancer cells. Other studies have demonstrated that the inhibitory growth effects of IL-32 were partly dependent on lymphocytes, dendritic cells and other cytokines (46,49).
These results indicated contradictory functions of IL-32 on tumour growth. It is possible that alternative splicing of IL-32 leads to discrepancies in functional studies. Heinhuis et al (23) revealed that 293 cells overexpressing IL-32β or IL-32γ underwent cell death, while human mammalian cell lines expressing high levels of IL-32α did not. These opposing functions have also been reported in the alternative splice variants of IL-6 and IL-24 (50,51). One function of IL-6 is to promote cell proliferation, but an alternatively spliced IL-6 variant can counteract this effect. Similarly, IL-24-induced cell death can be blocked by an IL-24 splice variant.
The motogenic properties of IL-32
IL-32 has also been demonstrated to influence tumour cell motility, a critical factor in tumour cell invasion and metastasis. In gastric cancer, Tsai et al (13) established stable IL-32-expressing cell sublines and revealed that all IL-32-overexpressing cells had protrusions at their leading edges with elongated, spindle-like morphology compared with that of the control cells. In addition to these morphological characteristics, IL-32-overexpressing cells displayed significantly higher invasive, metastatic and wound healing capacities compared with those of control cells. Similar observations were also repeatedly obtained in doxycycline-induced IL-32-overexpressing cells. This study also revealed that the underlying mechanism of IL-32-triggered cell invasion was an increase in the expression levels of IL-8, vascular endothelial growth factor (VEGF), matrix metalloproteinase (MMP)2 and MMP9, and activation of protein kinase B (Akt), β-catenin and hypoxia inducible factor 1α (HIF-1α) (13). These findings are in line with those of previous studies, which revealed that the IL-32-acquired invasive and migration phenotype of lung cancer was mediated through the co-expression of IL-8 and VEGF (40).
The involvement of IL-32 in tumour migration and invasion has also been demonstrated in breast cancer (15). Previous study has reported that overexpression of IL-32β increased tumour cell migration and invasion in human breast cancer cells. By contrast, knockdown of IL-32 negated these effects. Additionally, the motogenic effect of IL-32 was stimulated by IL-32β-induced VEGF (15). In addition, Guenin et al (52) demonstrated that IL-32 induced the migration of head and neck squamous cell carcinoma cells by regulating the expression of Snail. In HCC, IL-32α-expressing tumour cells invaded blood vessels, which may suggest an association between IL-32α expression and tumour metastasis (9). More recently, studies have revealed a motogenic effect of IL-32 in osteosarcoma and melanoma (53,54).
Taken together, these results suggested that IL-32 expression increases the migration and invasion capacities of tumour cells. By contrast, a recent study revealed that overexpression of a different IL-32 isoform (IL-32θ) in colon cells displayed a decrease in their invasiveness and in their oncogenic capabilities (55). Therefore, the detrimental role of IL-32 in multiple types of cancer may be clinically relevant.
The angiogenic properties of IL-32
In human pulmonary arterial hypertension and glioblastoma multiforme, hyper-proliferative endothelial cells (ECs) revealed a significant increase in IL-32 expression (56). Furthermore, suppression of IL-32 negatively affected the proliferation of ECs and downregulated expression levels of nitric oxide, IL-8 and MMP-9 in adult and neonatal ECs (56). Functional studies that used co-culture-based angiogenesis assays revealed an IL-32 increased tube formation in a dose-dependent manner. By contrast, an αVβ3 inhibitor attenuated this response and reduced the expression of IL-32γ-induced IL-8. These studies demonstrated that IL-32 promotes angiogenesis partially through the integrin αVβ3. The direct association between IL-32 and tumour angiogenesis remains undetermined, and associated studies are limited. In gastric cancer, IL-32 can induce the expression of IL-8, VEGF, MMP2 and MMP9 (13). Notably, IL-8 is a particularly well-established potent promoter of angiogenesis. IL-32 may indirectly promote tumour angiogenesis via inducing other cytokines and growth factors.
It may be beneficial to evaluate the angiogenic activity of IL-32 in human cancer, as angiogenesis serves a crucial role in the pathogenesis and progression of cancer. In summary, IL-32 is involved in multiple aspects of cancer development, including growth, migration and angiogenesis (Fig. 1).
The mechanisms of IL-32 in cancer
To directly investigate the mechanisms of IL-32-mediated tumour growth and metastasis, various human tumour cell lines have been transfected with the IL-32 gene. The effect of IL-32-transfection on tumour inhibition and promotion depends on the tumour cell type. For example, IL-32β-transfected breast cancer cells demonstrated stronger migration and invasion abilities than those of control tumour cells, and this process was mainly dependent on the IL-32β-VEGF-STAT3 pathway (15). In addition, Tsai et al (13) revealed that ectopic expression of IL-32 in gastric cancer cell lines increased metastatic potential via increased activity of Akt, β-catenin and HIF-1α. Tumour cells were also used to monitor cell survival and tumour development following transfection with IL-32-specific small interfering RNA. In pancreatic cancer, IL-32 suppression markedly stimulated apoptosis by downregulating anti-apoptotic proteins. This finding was confirmed in human HCC (9).
However, in chronic myeloid leukaemia, IL-32-transfected cells were more susceptible to NK cell-mediated killing than control tumour cells (47). In another study, IL-32 overexpression inhibited cancer development in cervical cancer cells compared with mock-control cells (41). Additionally, overexpression of IL-32 in colon and prostate cancer cell lines inhibited tumour growth. It was hypothesised that IL-32 may promote TNF-α-induced cell growth inhibition or induce death through the TNFR1 signalling pathway (14,48). Notably, in vivo tumour growth was significantly slower in mice with IL-32γ-transfected HCT116 colon cancer cells compared with control cells (45,46). Additionally, the anticancer effect of IL-32 was associated with the increased infiltration of CD8+ T cells, lymphocytes and NK cells.
These results illustrated the discrepant effects of IL-32 in cancer. The inconsistent observations among these results might originate from malignancy-specific variations in downstream pathways of IL-32. IL-32 is associated with various pathways, including the nuclear factor-κB and p38 mitogen-activated protein kinase pathways (18), extracellular signal-regulated kinase-1/2 and phosphoinositide 3-kinase/Akt pathways (57), a caspase-1-mediated pathway that can be synchronized with nucleotide-binding oligomerization domain-containing protein 1 and 2 ligands (58), and a caspase-3-dependent pathway (59), depending on the tumour type and tumour microenvironment (Fig. 1). Determining the modulatory effects of IL-32 on pathways is challenging, particularly since it may be affected by variations in the tumour microenvironment.
The regulation of IL-32 in cancer
Aberrant expression levels of IL-32 serve an important role in cancer, and therefore represent a potential therapeutic target. The mechanisms of IL-32 expression regulation in cancer have been studied by several groups. In epithelial cell-derived thyroid carcinoma (TC) (60), Plantinga et al (60) revealed that patients with TC have an overrepresentation of the ancient T allele, and lipopolysaccharide-induced expression of IL-32 was higher in cells homozygous for the ancient T allele than in cells without this allele. These results clearly reveal that genetic variations of IL-32 can lead to an increase in IL-32 gene expression. In addition, the transcription factor Oct4 also increased IL-32 expression at the mRNA and protein levels in colorectal cancer cells (61). It has been reported that microRNA-205 induces an increase in IL-32 mRNA and protein expression levels (62). These results are consistent with those of another study that revealed that the inhibition of miR-23b-3p induces a reduction in IL-32 expression in renal cancer (63). In summary, IL-32 expression levels appear to correlate with genetic factors, including genetic variations, transcription factor and microRNAs.
Using immunostaining and reverse transcription-polymerase quantitative chain reaction, Suga et al (16) revealed that IL-32 was more predominantly expressed in skin lesions of patients with cutaneous T-cell lymphoma than in normal skin, suggesting that hypoxia may contribute to the overexpression of IL-32. It has been confirmed that hypoxia induces IL-32 in human breast cancer cells (15,64); hypoxic challenges led to a time-dependent increase in the expression of IL-32 in breast cancer cells. A recent study reported that IL-32 was induced by hypoxia and secreted from multiple myeloma cells in extracellular vesicles (65). Furthermore, IL-32β expression levels were upregulated by a hypoxia mimetic chemical, CoCl2. These results demonstrated that hypoxia enhances the expression of IL-32, which may contribute to the progression and metastasis of human cancer. Additionally, acidic conditions also contribute to increases in IL-32 expression (66). Identification of the mechanisms underlying IL-32 modulation are required prior to this novel cytokine being used as a target in human cancer treatments.
Conclusion and future directions
Inflammatory microenvironments serve a critical role in tumorigenesis, imposing significant challenges in the design of effective cancer therapy. Among growth factors and cytokines, IL-32 may be an additional mediator of human cancer development and therefore may provide a novel therapeutic strategy. Understanding the biological activity of IL-32 in cancer progression requires a comprehensive analysis of the results obtained from clinical studies, cell cultures and animal models. Nevertheless, further investigations are required to elucidate the paradoxical role of IL-32 in cancer, which appears to be due in part to IL-32 isoforms and variations in the tumour microenvironment. It is apparent that various mechanisms are involved in IL-32 actions, including direct effects on tumour cell proliferation, angiogenesis and metastasis, and indirect effects via inflammatory cells, including neutrophils and macrophages. The mechanisms of the antitumour effect of IL-32 must be identified, and tumour-stimulating actions must be neutralised. Identifying the optimal IL-32 isoform to function in a particular disease may indicate new directions for the development of antitumor strategies.
Acknowledgements
Not applicable.
Funding
The present study was supported by the National Natural Science Foundation of China (grant nos. 91429302, 81201868 and 81560030).
Availability of data and materials
Not applicable.
Authors' contributions
ZC and HY designed and conceived the study. DH, XH, EZ, QC, RX, XL, FZ and ZC provided advice and assistance. HY wrote the manuscript. All authors have contributed to and approved the final manuscript.
Ethics approval and consent to participate
Not applicable.
Consent for publication
Not applicable.
Competing interests
The authors declare that they have no competing interests.
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