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microRNA-365, down-regulated in colon cancer, inhibits cell cycle progression and promotes apoptosis of colon cancer cells by probably targeting Cyclin D1 and Bcl-2

Jing NieDepartment of Molecular Biology, PLA General Hospital, 28 Fuxing Road, Beijing 100853, ChinaLin LiuDepartment of General Surgery, PLA General Hospital, 28 Fuxing Road, Beijing 100853, ChinaWei ZhengDepartment of General Surgery, PLA General Hospital, 28 Fuxing Road, Beijing 100853, ChinaLin ChenDepartment of General Surgery, PLA General Hospital, 28 Fuxing Road, Beijing 100853, ChinaXin WuDepartment of General Surgery, PLA General Hospital, 28 Fuxing Road, Beijing 100853, ChinaYingxin XuDepartment of General Surgery, PLA General Hospital, 28 Fuxing Road, Beijing 100853, ChinaXiaohui DuDepartment of General Surgery, PLA General Hospital, 28 Fuxing Road, Beijing 100853, ChinaWeidong Han
2011en
ABI

Аннотация

Deregulated microRNAs participate in carcinogenesis and cancer progression, but their roles in cancer development remain unclear. In this study, miR-365 expression was found to be downregulated in human colon cancer tissues as compared with that in matched non-neoplastic mucosa tissues, and its downregulation was correlated with cancer progression and poor survival in colon cancer patients. Functional studies revealed that restoration of miR-365 expression inhibited cell cycle progression, promoted 5-fluorouracil-induced apoptosis and repressed tumorigenicity in colon cancer cell lines. Furthermore, bioinformatic prediction and experimental validation were used to identify miR-365 target genes and indicated that the antitumor effects of miR-365 were probably mediated by its targeting and repression of Cyclin D1 and Bcl-2 expression, thus inhibiting cell cycle progression and promoting apoptosis. These results suggest that downregulation of miR-365 in colon cancer may have potential applications in prognosis prediction and gene therapy in colon cancer patients.

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