RAB27A promotes the proliferation and invasion of colorectal cancer cells

异位表达 基因敲除 结直肠癌 癌症 克隆(Java方法) 癌症研究 细胞生长 生物 癌细胞 细胞培养 遗传学 基因
作者
Qingyan Li,Huixia Zhao,Wei Dong,Na Guan,Hu Y,Zhi-Yan Zeng,He Zhang,Fengyun Zhang,Qiuwen Li,Jingwen Yang,Xiao Wang
出处
期刊:Scientific Reports [Nature Portfolio]
卷期号:12 (1) 被引量:4
标识
DOI:10.1038/s41598-022-23696-7
摘要

Colorectal cancer (CRC) is one of the most commonly diagnosed cancer types worldwide. Despite significant advances in prevention and diagnosis, CRC is still one of the leading causes of cancer-related mortality globally. RAB27A, the member of RAB27 family of small GTPases, is the critical protein for intracellular secretion and has been reported to promote tumor progression. However, it is controversial for the role of RAB27A in CRC progression, so we explored the exact function of RAB27A in CRC development in this study. Based on the stable colon cancer cell lines of RAB27A knockdown and ectopic expression, we found that RAB27A knockdown inhibited proliferation and clone formation of SW480 colon cancer cells, whereas ectopic expression of RAB27A in RKO colon cancer cells facilitated cell proliferation and clone formation, indicating that RAB27A is critical for colon cancer cell growth. In addition, our data demonstrated that the migration and invasion of colon cancer cells were suppressed by RAB27A knockdown, but promoted by RAB27A ectopic expression. Therefore, RAB27A is identified as an onco-protein in mediating CRC development, which may be a valuable prognostic indicator and potential therapeutic target for CRC.

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