miR-150-504-519d inhibits the growth of human colorectal cancer cell line SW48 and downregulates c-FLIP receptor

被引:6
作者
Rong, Guoqiang [1 ]
Yang, Xiaodong [2 ]
Wu, Haorong [2 ]
Wu, Yongyou [2 ]
机构
[1] Fifth Peoples Hosp Changshu, Dept Gen Surg, Changshu, Jiangsu, Peoples R China
[2] Soochow Univ, Affiliated Hosp 2, Dept Gen Surg, 1055 Sanxiang Rd, Suzhou 215004, Jiangsu, Peoples R China
关键词
cell growth; c-FLIP; colorectal cancer (CRC); miR-150-504-519d; transfection; MICRORNAS; OVEREXPRESSION; PROLIFERATION; BIOGENESIS; MECHANISMS; EXPRESSION; APOPTOSIS; MIGRATION; MIRNAS; EMT;
D O I
10.1002/jcb.28073
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
microRNAs (miRNAs) are noncoding RNAs that regulates the expression of target messenger RNAs (mRNAs). c-FLIP is an inhibitor of cell apoptosis through inhibition of caspase 8. miR-150, miR-504, and miR-519d were related to cancer cell proliferation, invasion, and migration in colorectal cancer (CRC). However, the role of miR-150-504-519d in CRC has not been studied and the relationship between miR-150-504-519d and c-FLIP remains unclear. In this study, we found that c-FLIP was upregulated in CRC tissues, without detectable expression in normal CRC tissues. Using SW48 cell line, we further showed that miR-150-504-519d inhibited migration, invasion, and promoted apoptosis of SW48 cells. Moreover, in SW48 cell line transfected with miR-150-504-519d, the protein expression of c-FLIP was significantly lower compared with cells transfected with scramble. Our results demonstrated upregulation of c-FLIP in CRC, which was downregulated in SW48 cells after the transfection of miR-150-504-519d, suggesting that manipulation of miR-150-504-519d expression might be a novel approach for the treatment of colorectal cancer.
引用
收藏
页码:7962 / 7969
页数:8
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