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首页> 外文期刊>Tumour biology : >MicroRNA-455 inhibits proliferation and invasion of colorectal cancer by targeting RAF proto-oncogene serine/threonine-protein kinase
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MicroRNA-455 inhibits proliferation and invasion of colorectal cancer by targeting RAF proto-oncogene serine/threonine-protein kinase

机译:MicroRNA-455通过靶向RAF原癌基因丝氨酸/苏氨酸蛋白激酶抑制结直肠癌的增殖和侵袭

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Colorectal cancer (CRC, also known as colon cancer, rectal cancer, or bowel cancer) is the second leading cause of cancer mortality in the Western world. MicroRNAs (miRNAs) are a class of small (18-25 nucleotides long) noncoding RNAs with important posttranscriptional regulatory functions. miRNAs play important roles in various physiological and pathological processes including carcinogenesis in various solid cancers including CRC. In order to investigate the roles that miRNAs played in CRC, the expression of human miRNAs (in 20 normal adjacent tissue samples and 20 colon cancer samples) was examined in this study. miR-455, miR-484, and miR-101 were significantly downregulated in colon cancer samples. And overexpression of miR-455 significantly inhibited the proliferation and the invasion of SW480, but had no effect on apoptosis. PCR and Western blot showed that overexpression of miR-455 decreased protein expression of RAF proto-oncogene serine/threonine-protein kinase (RAF1) but had no effect on mRNA level. Luciferase assay indicated that miR-455 regulated RAF1 expression directly. Moreover, overexpression of RAF1 partially reversed the inhibitory effect of miR-455 on the growth and the invasion of SW480. The data indicated that miR-455 regulates the proliferation and invasion of colorectal cancer cells, at least in part, by downregulating RAF1, a direct target of miR-455. Collectively, our study demonstrated that miR-455-RAF1 may represent a new potential therapeutic target for colorectal carcinoma treatment.
机译:大肠癌(CRC,也称为结肠癌,直肠癌或肠癌)是西方世界导致癌症死亡的第二大原因。微小RNA(miRNA)是一类小的(18-25个核苷酸长)非编码RNA,具有重要的转录后调控功能。 miRNA在包括CRC在内的各种实体癌中的各种生理和病理过程(包括致癌作用)中都起着重要作用。为了研究miRNA在CRC中的作用,在本研究中检查了人类miRNA的表达(在20个正常邻近组织样本和20个结肠癌样本中)。 miR-455,miR-484和miR-101在结肠癌样本中显着下调。 miR-455的过表达显着抑制SW480的增殖和侵袭,但对细胞凋亡没有影响。 PCR和Western印迹显示miR-455的过表达降低了RAF原癌基因丝氨酸/苏氨酸蛋白激酶(RAF1)的蛋白表达,但对mRNA水平没有影响。萤光素酶测定表明miR-455直接调节RAF1表达。此外,RAF1的过表达部分逆转了miR-455对SW480的生长和侵袭的抑制作用。数据表明,miR-455至少部分地通过下调miR-455的直接靶标RAF1来调节大肠癌细胞的增殖和侵袭。总体而言,我们的研究表明miR-455-RAF1可能代表了结直肠癌治疗的新潜在治疗靶标。

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