Functions and underlying mechanisms of miR-650 in human cancers

Hepatocellular carcinoma (HCC), the most frequent primary cancer, is the third major cause of tumor-related deaths [25]. It has the characteristics of a high degree of malignancy, poor treatment response and unfavourable prognosis [26] and represents a heavy public health burden. Multiple risk factors [27‐29] involved in the complex process of HCC have been widely reported, among which miR-650 is one of the key molecules. For the past few years, dysregulation of miR-650 in HCC has been widely reported. Han et al. [30] found that miR-650 expression significantly overexpressed in HCC tissues, especially in patients with tumour metastasis. Qin’s et al. [31] research revealed that the expression of Axin, which can inhibit the progression of HCC by targeting miR-650, was weak in HCC. Moreover, the overexpression of miR-650, which can be stimulated with benzo[a]pyrene, promotes the pathological process of fatty liver disease and HCC, as implicated in the work of Ge et al. [32]. Another bioinformatic analysis also demonstrated that the relative quantification of miR-650 in liver tissue was markedly increased in non-alcoholic steatohepatitis (NASH) groups [33]. In addition, elevated miR-650 expression was significantly associated with patient differentiation capability and advanced tumour TNM stage [34]. These findings combined with the above data based on cell lines and clinical samples indicate that miR-650 functions as a tumour promoter in HCC. As discussed above, the progression of HCC is closely related to the expression of miR-650, making it a promising biomarker and therapeutic target for the early prevention and applicable treatment of HCC. Nevertheless, the antitumour effect of miR-650 has rarely been reported in HCC.

Approximately 2.2 million cases of lung cancer (LC) were newly increased in 2020. LC causes the most cancer-induced deaths (18.0% of total cancer deaths) [35], of which non-small-cell lung cancer (NSCLC) accounts for the majority [36]. Accumulating studies have indicated that miR-650 acts as a tumour promoter in LC, including NSCLC and lung adenocarcinoma (LAD). In the present study, miR-650 was shown to highly express in NSCLC. Huang et al. [16] found that the expression level of miR-650 was substantially higher in LAD tissue samples than in adjacent normal controls. Moreover, the overexpression of miR-650 was dramatically correlated with the clinical characteristics of LAD patients, such as advanced tumour stage, high incidence of lymph node metastasis, and unfavourable prognosis [16]. Furthermore, downregulation of miR-650 reversed the docetaxel resistance of LAD cells [16]. Another study demonstrated that miR-650 overexpressed in NSCLC, and in vitro experiments indicated that miR-650 promoted the cancer cell proliferation and migration, which resulted in low overall survival date of NSCLC patients [13]. Moreover, a miR-650 inhibitor was shown to attenuate si-MEG3-induced promotion of the LC stem cell-like state, migration and invasion in NSCLC [37]. In spite of great advances in diagnostic and therapeutic methods, the overall survival rate of NSCLC patients is still below 15% [38]. Thus, more efforts are needed to explore new effective strategies for the diagnosis and clinical treatment of LC.

According to Global Cancer Statistics, more than 1.9 million new cases of colorectal cancer (CRC) were estimated to occur in 2020, causing 935,000 deaths globally. Tumour metastasis develops in approximately 10% of patients in stage I or II and eventually leads to death within 5 years after exsection [39]. Currently, dysregulation of miR-650 has been researched in CRC, and miR-650 has been reported to act as both a tumour promoter or suppressor; therefore, the role and function of miR-650 in CRC remain controversial. Zhou et al. [39] discovered that the expression of miR-650 in CRC tissues positively correlated with the overall survival of patients. Furthermore, it repressed high-risk non-metastatic CRC progression [39] by inhibiting cell growth and invasion. In contrast, some reports have shown that miR-650 is upregulated and functions as an oncogene in CRC [14, 40‐42]. Based on what we already know, there is seemingly no consensus about the expression and function of miR-650 in CRC progression. Thus, more research is needed to comprehensively explore the roles of miR-650 in CRC.

Gastric cancer (GC) was responsible for approximately 769,000 deaths in 2020, ranking fourth in mortality and fifth in incidence [43] globally. Due to the diagnosis of GC at early stages with complications, limited treatment options and poor prognoses, GC remains a great clinical challenge [44]. At present, the standard diagnostic methods for GC patients are gastroscopy and biopsy, but the utility of these methods is limited largely due to the invasiveness of GC and limited medical resources [45]. miR-650, as a new tumour biomarker in GC, has been investigated in recent years. One bioinformatic study based on 180 GC patients and 45 healthy individuals indicated that elevated miR-650 expression levels was significantly correlated with the existence of GC [45] and miRNA-650 are evaluated to be a promising and powerful non-invasive biomarker for the detection of GC. Previously, Zhang et al. [15] reported that overexpression of miR-650 promoted GC tumorigenesis in vivo and GC cell clonogenicity in vivo. Moreover, the overexpression of miR-650 has a positively association with the advancement of GC, as demonstrated in the work of Liu et al. [46] and An et al. [47].

Glioma, the most common primary tumour in the brain, accounts for approximately one-third of malignant cancers of the central nervous system [48]. Sun et al. [49] found that miR-650 expression was critically increased in glioma tissues and that was more frequently explored in tumours with a high WHO grade or low Karnofsky performance score (P < 0.001). Another study reported that miR-650 overexpressed in glioma tissues and cell lines. Furthermore, intensive expression was significantly correlated with the advanced tumour stage, lymph node metastasis and poor prognoses in glioma patients [50]. In contrast, Xu et al. [51] found that miR-650 was expressed at a low level in glioma tissues and in vitro cell lines.

Cutaneous melanoma is a common tumour derived from the epidermis and mucosa [52]; it comprises 4-10% of all malignant cancers and is correlated with 75% of skin cancer-related deaths [53]. The death rates associated with melanoma have reportedly dropped rapidly after the introduction of new therapies, including targeted therapies for melanoma metastasis and immune checkpoint inhibitors [54, 55]. Liu et al. [56] recently found that the regulation of miR-650 has a negative correlation with melanoma progression. Moreover, further study showed that miR-650 overexpression alleviated MGMT-induced DTIC resistance in melanoma by increasing cell apoptosis [19], which indicated that miR-650 was a novel biomarker of great value for the evaluation of melanoma.

As the most frequent malignancy of the bone marrow, acute myeloid leukaemia (AML) has a high fatality rate [35]. Yuan et al. [57] revealed that miR-650 expression was reduced in AML, which contributed to leukaemia progression. Similarly, Gaine et al. [58] found that the expression of the erythropoietin receptor (EPOR) in t(12;21) B-ALL cells was higher than that in normal samples. Notably, EPOR expression is influenced by GATA2 and has an inverse correlation with miR-650 expression [58]. One study published in Blood reported that overexpression of miR-650 is correlated with a favourable chronic lymphocyte leukaemia (CLL) prognosis and affects the oncogenic capacity of B cells [24]. Furthermore, multivariate analysis showed that overexpression of miR-650 is an available independent predictor of survival and time to first treatment (TTFT) [24]. However, an inconsistent report that partly argued against the results above showed a significant increase in miR-650 expression in CLL patients [59]. Hence, the association between leukaemia and miR-650 needs further verification by expanding the number of patient samples included in the current work.

miR-650 has also been found to serve as an oncogene that is upregulated in various other cancers. In breast cancer, overexpression of miR-650 has been observed to induce the downregulation of the tumour suppressor ING4, which we previously mentioned is significantly correlated with EMT of breast cancer cells [60]. Another recent study revealed that the expression level of miR-650 is upregulated in EC, resulting in the progression of EC through the SMAD7-TGF-β (transforming growth factor-β) pathway [11]. In addition, miR-650 overexpressed in anaplastic thyroid carcinoma (ATC), where it promotes the proliferation and motility of cancer cells by targeting Protein Phosphatase 2 Catalytic Subunit Alpha (PPP2CA) [61]. In osteosarcoma, miR-650 has been reported to function as an oncogene. Yun et al. [18] revealed that overexpressing miR-650 decreased ING4 expression in human osteosarcoma cells and increased IL-6 transcription. Both ING-4 and IL-6 could modulate osteoblast and osteoclast differentiation. Moreover, miR-650 could upregulate the transcriptional activity of NF κB [18] and reduce the quantity of nuclear factor (NF) of κ light polypeptide gene enhancer. Interestingly, similarly significant upregulation of miR-650 has been observed in oral cancer, and the expression of miR-650 has been positively correlated with cancer cell proliferation, migration and invasion [62]. Likewise, Zuo et al. [63] reported that miR-650 could function as an onco-miR in prostate cancer by suppressing cellular stress response (CSR1) expression.

Overall, these findings have revealed that the profile of miR-650 expression depends on the type of cancer and that miR-650 is involved in the occurrence and development of various cancers. The overall expression files of miR-650 in various cancers and relative clinical features are presented in Tables 1 and 2. Even so, more studies are required to further explore the expression profiles of miR-650 in tumours.

In parallel with the overexpression and clinical features discussed above, miR-650 also conferred more oncogenicity to tumour cells. In HCC, existing evidence indicates that upregulation of miR-650 modulates cell proliferation, apoptosis, migration and invasion [30‐32, 34] of cancer cells. In terms of the mechanism, miR-650 functions as an upstream signal of the large tumor suppressor kinase 2 gene (LATS2)/YAP (Ser127) signalling pathway and regulates its downstream target genes [30]. Moreover, Ye et al. [64] also revealed that miR-650 could serve as an onco-miR to potentiate cell growth and metastasis by directly targeting LATS2 in NSCLC formation and progression. Interestingly, Liu et al. [46] reported that miR-650 downregulation inhibited proliferation, expedited apoptosis and reduced the migration of HP + GC cells. Moreover, miR-650 mediated the Hippo pathway via the PBX1/miR-650/LATS axis. As a molecular sponge of Axin1, miR-650 enhanced the Wnt signalling pathway to facilitate tumour progression [31]. Furthermore, Ge et al. [32] found that miR-650 in benzo[a]pyrene-exposed cancer cells contributed to HCC metastasis by directly targeting suppressor of cytokine signalling 3 (SOCS3), and this inhibition modulated the activation of the Janus kinase (JAK)/ signal transducer and activator of transcription 3(STAT3) cascade. The study from Zhao et al. [37] suggested that miR-650 silencing inhibited the vital capacity and invasion ability of large-cell carcinomas (LCCs) and lung cancer stem cells (LCSCs) (H1299 cell lines) through the lncRNA maternally expressed gene 3(MEG3)/miR-650/solute carrier family 34 member 2 (SLC34A2) axis. Moreover, ING4 is also a vital gene targeted by miR-650 to facilitate cell proliferation and invasion and induce a stem cell-like state in LC [13, 16]. With regard to CRC, Zhou et al. [40] argued that MIR155HG, as an endogenous lncRNA, competed with annexin 2 (ANXA2) by combining with miR-650, thereby promoting M2 macrophage polarization and oxaliplatin resistance in CRC cells. In another study, decreased luciferase activity of miR-650 was observed with the 3’ untranslated region of N-myc downstream regulated gene 2 (NDRG2) inserted downstream of the luciferase gene, indicating that NDRG2 was directly targeted by miR-650 [65]. Notably, other researchers have observed that inhibition of miR-650 facilitates more apoptosis in CLL cells [59]. Further studies have demonstrated that NDRG2 expression can be significantly downregulated by miR-650 simultaneously with p53 aberrations [59]. It is worth mentioning that other researchers have found that constructed adenoviruses carrying the NDRG2 gene heightened p53-mediated apoptosis of HCC cells [66]. Moreover, CSR1 has also been reported to be a shared gene targeted by miR-650 in both GC [47] and prostate cancer [63]. In addition to cell proliferation and apoptosis, overexpression of miR-650 induces EMT of cancer cells [11, 14, 30, 49, 67], which is a key factor in promoting the metastasis of tumours [68]. Functional analyses in Jin’s study demonstrated that upregulated miR-650 expression heightened the migration of glioma cells through EMT promotion. Additionally, they found that miR-650 could inhibit glioma cell adhesion and promote autophagy. Mechanistically, NF-κB1 upregulated miR-650 expression by directly interacting with its promoter, and then the AKT/ extracellular regulated protein kinases (ERK) and NF-κB pathways were enhanced by miR-650 via the RAS-like, estrogen-regulated growth inhibitor (RERG)-PH domain and leucine rich repeat protein phosphatase 2 (PHLPP2) complex [50].

As a valued member of the ING family, ING4 has been revealed to function as a formidable tumour suppressor due to its significant role in the modification of chromatin modification, cell growth, cell invasion and vascularization [69, 70]. However, it has been revealed to be frequently decreased in various human tumours, and the variation in ING4 markedly contributes to cancer development. Interestingly, accumulating studies have suggested that ING4 is a downstream target of miR-650 in many types of cancer, such as HCC [34], LC [13, 16], CRC [14], GC [15], and BC [60]. Finally, You et al. [14] demonstrated that miR-650 could function as a tumour promoter and enhance the malignant phenotype of CRC. In terms of the mechanism, miR-650 targets ING4, leading to CRC progression promoted by the ERK/p38 mitogen-activated protein kinases (MAPK) pathway. Analogously, another study further suggested that miR-650 increased caspase-3-dependent cell apoptosis by regulating Bcl-2/Bax expression [16] via ING4. Interestingly, Tang et al. [13] revealed that miR-650 promotes NSCLC cell proliferation and migration through the ING4/Wnt-1/β-catenin pathway. Combined, these results suggest that ING4 is a significant regulator of the signalling pathways in the tumorigenic progress of miR-650 and provides promising biomarker and therapeutic target for human cancer.

In contrast with the aforementioned investigations, miR-650 has also been reported to function as a tumour suppressor by arresting the cell cycle, inhibiting cell proliferation and weakening the malignant phenotype in tumours. In CRC, there is no consensus about the function of miR-650 thus far. Zhou et al. [39] found that miR-650 inhibited cell growth and migration by suppressing the AKT2/ Glycogen synthase kinase (GSK3β)/E-cadherin pathway. Another bioinformatic study revealed a similar conclusion [41, 42]. Therefore, to further explore the roles of miR-650, more related studies are needed. In addition, rescue experiments in Xu’s et al. [51] study showed that miR-650 could inhibit cell growth by targeting family with sequence similarity 83member F (FAM83F) in glioma. In addition, the lncRNA POU3F3/miR-650/MGMT pathway has been revealed to function critically in DTIC resistance in melanoma [19]. In terms of the mechanism, lncRNA POU3F3 works as a competitive RNA to combine with miR-650; therefore, MGMT expression rises to a higher extent [19] in melanoma cells. Additionally, Liu et al. [56] revealed that miR-650 contained cell proliferation and invasion while exerting on adverse effect on cell apoptosis in cutaneous melanoma via the lncRNA ZFPM2-AS1/miR-650/NOTCH1 axis in melanoma. An article published in Blood indicated that overexpression of miR-650 led to the decreased proliferative capacity of B cells [24]. Mechanistically, miR-650 targeted essential proteins in cell proliferation, namely, cyclin-dependent kinase (CDK1), ING4, and EBF3 in B cells. A cell transfection experiment with miR-650 revealed significant downregulation of signalling molecule levels of EBF3, ING4 and CDK1 by 67%, 64%, and 53%, respectively. This finding validates the correlation of these three proteins with miR-650 in B cells. Moreover, Mraz et al. [24] found that miR-650 was modulated by coupling expression with its homologous gene for immunoglobulin lambda. This observation is surprising because previous studies demonstrated that miR-650 has an independent expression of immunoglobulin [23].