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MicroRNA-874 Functions as a Tumor Suppressor by Targeting Cancer/Testis Antigen HCA587/MAGE-C2
Xiao Song1, Wenjie Song1, Ying Wang1
1Department of Immunology, School of Basic Medical Sciences, Key Laboratory of Medical Immunology (Ministry of Health), Peking University Health Science Center, Beijing, China.
Abstract:
Cancer/testis antigen HCA587/MAGE-C2 has been considered as a tumor specific target for immunotherapy. It has been reported that HCA587/MAGE-C2 plays an active role in tumorigenesis by promoting the growth and survival of tumor cells. However, the regulation of HCA587/MAGE-C2 expression in cancer cells remains largely unknown. MicroRNAs (miRNAs), a large family of gene regulators, have been shown to negatively regulate the expression of important cancer-related genes and contribute to the initiation and development of cancers. In this study, we conducted searches of miRNAs that regulate HCA587/MAGE-C2 expression. We combined bioinformatics tools with biological validation assays to demonstrate that HCA587/MAGE-C2 is a direct target of microRNA-874 (miR-874). Furthermore, we investigated the expression levels of miR-874 in human hepatocellular carcinoma tissues and paired adjacent normal tissues by stem-loop reverse transcription-quantitative polymerase chain reaction (RT-qPCR). The results revealed a significant downregulation of miR-874 expression in tumor tissues compared to adjacent normal tissues. Finally, we demonstrated that overexpression of miR-874, as well as HCA587/MAGE-C2 silencing, resulted in suppression of tumor cell proliferation and invasion. Moreover, the inhibition effects of miR-874 on cell proliferation and invasion were reversed by co-expression of HCA587/MAGE-C2 in A375 cells. Taken together, our data demonstrated that HCA587/MAGE-C2 is a direct target of miR-874, and miR-874 may function as a tumor suppressive miRNA, at least in part, by negatively regulating HCA587/MAGE-C2 expression in cancer cells.
Insights
MicroRNA-874 (miR-874) targets cancer antigen HCA587/MAGE-C2, suppressing tumor growth. This study found miR-874 is downregulated in hepatocellular carcinoma, suggesting its tumor-suppressive role.
Area of Science:
- Oncology
- Molecular Biology
- Gene Regulation
Background:
- Cancer/testis antigen HCA587/MAGE-C2 promotes tumor cell growth and survival.
- Regulation of HCA587/MAGE-C2 expression in cancer is not well understood.
- MicroRNAs (miRNAs) are key regulators of gene expression implicated in cancer development.
Purpose of the Study:
- To identify miRNAs regulating HCA587/MAGE-C2 expression.
- To investigate the role of miR-874 in hepatocellular carcinoma (HCC).
- To elucidate the functional relationship between miR-874 and HCA587/MAGE-C2 in cancer cells.
Main Methods:
- Bioinformatics analysis to predict miRNA targets.
- Biological validation assays to confirm direct targeting.
- Stem-loop reverse transcription-quantitative polymerase chain reaction (RT-qPCR) to measure miRNA expression.
- Cell proliferation and invasion assays.
- Gene silencing and overexpression studies.
Main Results:
- HCA587/MAGE-C2 was identified as a direct target of microRNA-874 (miR-874).
- miR-874 expression was significantly downregulated in human hepatocellular carcinoma tissues.
- Overexpression of miR-874 suppressed tumor cell proliferation and invasion.
- HCA587/MAGE-C2 silencing also inhibited tumor cell proliferation and invasion.
- The tumor-suppressive effects of miR-874 were reversed by co-expression of HCA587/MAGE-C2.
Conclusions:
- HCA587/MAGE-C2 is a direct target of miR-874.
- miR-874 acts as a tumor suppressor miRNA in cancer cells.
- miR-874 exerts its tumor-suppressive function, at least partly, by downregulating HCA587/MAGE-C2 expression.
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