miR-372 regulates cell cycle and apoptosis of ags human gastric cancer cell line through direct regulation of LATS2

被引:207
作者
Cho, Wha Ja [2 ]
Shin, Jeong Min [1 ]
Kim, Jong Soo [1 ]
Lee, Man Ryul [1 ]
Hong, Ki Sung [1 ]
Lee, Jun-Ho [1 ]
Koo, Kyoung Hwa [1 ]
Park, Jeong Woo [3 ]
Kim, Kye-Seong [1 ]
机构
[1] Hanyang Univ, Coll Med, Dept Anat & Cell Biol, Seoul 133791, South Korea
[2] Univ Ulsan, Coll Med, Ulsan Univ Hosp, Biomed Res Ctr, Ulsan 682060, South Korea
[3] Univ Ulsan, Dept Biol Sci, Ulsan 680749, South Korea
关键词
AGS gastric cancer cell line; apoptosis; cell cycle; G(2)-M transition; LATS2; miR-372; PUTATIVE TUMOR-SUPPRESSOR; HUMAN LUNG CANCERS; SMALL RNAS; MICRORNAS; EXPRESSION; HOMOLOG;
D O I
10.1007/s10059-009-0158-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Previously, we have reported tissue- and stage-specific expression of miR-372 in human embryonic stem cells and so far, not many reports speculate the function of this microRNA (miRNA). In this study, we screened various human cancer cell lines including gastric cancer cell lines and found first time that miR-372 is expressed only in AGS human gastric adenocarcinoma cell line. Inhibition of miR-372 using antisense miR-372 oligonucleotide (AS-miR-372) suppressed proliferation, arrested the cell cycle at G2/M phase, and increased apoptosis of AGS cells. Furthermore, AS-miR-372 treatment increased expression of LATS2, while over-expression of miR-372 decreased luciferase reporter activity driven by the 3' untranslated region (3' UTR) of LATS2 mRNA. Over-expression of LATS2 induced changes in AGS cells similar to those in AGS cells treated with AS-miR-372. Taken together, these findings demonstrate an oncogenic role for miR-372 in controlling cell growth, cell cycle, and apoptosis through down-regulation of a tumor suppressor gene, LATS2.
引用
收藏
页码:521 / 527
页数:7
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