Tazarotene-induced gene 1 interacts with Polo-like kinase 2 and inhibits cell proliferation in HCT116 colorectal cancer cells

被引:7
作者
Wang, Chun-Hua [1 ,2 ]
Lu, Tzung-Ju [2 ,3 ]
Wang, Lu-Kai [4 ]
Wu, Chang-Chieh [5 ]
Chen, Mao-Liang [6 ]
Kuo, Chan-Yen [6 ]
Shyu, Rong-Yaun [7 ]
Tsai, Fu-Ming [6 ]
机构
[1] Buddhist Tzu Chi Med Fdn, Taipei Tzu Chi Hosp, Dept Dermatol, New Taipei, Taiwan
[2] Tzu Chi Univ, Sch Med, Hualien, Taiwan
[3] Buddhist Tzu Chi Med Fdn, Taipei Tzu Chi Hosp, Dept Surg, Div Colon & Rectal Surg, New Taipei, Taiwan
[4] Chang Gung Univ, Inst Radiol Res, Radiat Biol Core Lab, Chang Gung Mem Hosp, Taoyuan, Taiwan
[5] Natl Def Med Ctr, Triserv Gen Hosp, Dept Surg, Keelung Branch, Keelung, Taiwan
[6] Buddhist Tzu Chi Med Fdn, Taipei Tzu Chi Hosp, Dept Res, New Taipei 231, Taiwan
[7] Buddhist Tzu Chi Med Fdn, Taipei Tzu Chi Hosp, Dept Internal Med, New Taipei, Taiwan
关键词
cell proliferation; cyclin E1; Fbxw7; Polo-like kinases; tazarotene-induced gene 1; ACID RECEPTOR-BETA; PROGNOSTIC-SIGNIFICANCE; CENTRIOLE DUPLICATION; EPIGENETIC CHANGES; DNA METHYLATION; BREAST-CANCER; EXPRESSION; TIG1; RARRES1; CARCINOMAS;
D O I
10.1002/cbin.11681
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Tazarotene-induced gene 1 (TIG1) is considered to be a tumor suppressor gene that is highly expressed in normal or well-differentiated colon tissues, while downregulation of TIG1 expression occurs in poorly differentiated colorectal cancer (CRC) tissues. However, it is still unclear how TIG1 regulates the tumorigenesis of CRC. Polo-like kinases (Plks) are believed to play an important role in regulating the cell cycle. The performance of PLK2 in CRC is negatively correlated with the differentiation status of CRC tissues. Here, we found that PLK2 can induce the growth of CRC cells and that TIG1 can prevent PLK2 from promoting the proliferation of CRC cells. We also found that the expression of PLK2 in CRC cells was associated with low levels of Fbxw7 protein and increased expression of cyclin E1. When TIG1 was coexpressed with PLK2, the changes in Fbxw7/cyclin E1 levels induced by PLK2 were reversed. In contrast, silencing TIG1 promoted the proliferation of CRC, and when PLK2 was also silenced, the proliferation of CRC cells induced by TIG1 silencing was significantly inhibited. The above research results suggest that TIG1 can regulate the tumorigenesis of CRC by regulating the activity of PLK2.
引用
收藏
页码:2347 / 2356
页数:10
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