Lithocholic Acid Induces miR21, Promoting PTEN Inhibition via STAT3 and ERK-1/2 Signaling in Colorectal Cancer Cells

被引:0
|
作者
Thinh-Thi Nguyen [1 ,2 ]
Thuan-Trong Ung [1 ,2 ]
Li, Shinan [1 ]
Sah, Dhiraj Kumar [1 ]
Park, Sun-Young [1 ]
Lian, Sen [3 ]
Jung, Young-Do [1 ]
机构
[1] Chonnam Natl Univ Med Sch, Res Inst Med Sci, Gwangju 501190, South Korea
[2] Nanogen Pharmaceut Biotechnol Joint Stock Co, Ho Chi Minh City 71207, Vietnam
[3] Southern Med Univ, Sch Basic Med Sci, Dept Biochem & Mol Biol, Guangzhou 510515, Peoples R China
基金
新加坡国家研究基金会; 中国国家自然科学基金;
关键词
miR21; lithocholic acid; colorectal cancer; STAT3; PTEN; MIR-21; MICRORNA-21; EXPRESSION; PROLIFERATION; APOPTOSIS; ACTIVATION; BIOMARKER; TRANSCRIPTION; SIGNATURE; CARCINOMA;
D O I
10.3390/ijms221910209
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
Micro-RNA-21 (miR-21) is a vital regulator of colorectal cancer (CRC) progression and has emerged as a potential therapeutic target in CRC treatment. Our study using real-time PCR assay found that a secondary bile acid, lithocholic acid (LCA), stimulated the expression of miR21 in the CRC cell lines. Promoter activity assay showed that LCA strongly stimulated miR21 promoter activity in HCT116 cells in a time- and dose-dependent manner. Studies of chemical inhibitors and miR21 promoter mutants indicated that Erk1/2 signaling, AP-1 transcription factor, and STAT3 are major signals involved in the mechanism of LCA-induced miR21 in HCT116 cells. The elevation of miR21 expression was upstream of the phosphatase and tensin homolog (PTEN) inhibition, and CRC cell proliferation enhancement that was shown to be possibly mediated by PI3K/AKT signaling activation. This study is the first to report that LCA affects miR21 expression in CRC cells, providing us with a better understanding of the cancer-promoting mechanism of bile acids that have been described as the very first promoters of CRC progression.
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页数:17
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