ZFP36L1 and ZFP36L2 inhibit cell proliferation in a cyclin D-dependent and p53-independent manner

被引:60
|
作者
Suk, Fat-Moon [1 ,2 ]
Chang, Chi-Ching [2 ,3 ]
Lin, Ren-Jye [4 ]
Lin, Shyr-Yi [5 ,6 ]
Liu, Shih-Chen [4 ]
Jau, Chia-Feng [4 ]
Liang, Yu-Chih [4 ,7 ,8 ]
机构
[1] Taipei Med Univ, Wan Fang Hosp, Div Gastroenterol, Dept Internal Med, Taipei, Taiwan
[2] Taipei Med Univ, Sch Med, Dept Internal Med, Coll Med, Taipei, Taiwan
[3] Taipei Med Univ Hosp, Div Rheumatol Immunol & Allergy, Taipei, Taiwan
[4] Taipei Med Univ, Sch Med Lab Sci & Biotechnol, Coll Med Sci & Technol, Taipei, Taiwan
[5] Taipei Med Univ Hosp, Dept Primary Care Med, Taipei, Taiwan
[6] Taipei Med Univ, Sch Med, Dept Gen Med, Coll Med, Taipei, Taiwan
[7] Taipei Med Univ Hosp, Tradit Herbal Med Res Ctr, Taipei, Taiwan
[8] Taipei Med Univ, Coll Med Sci & Technol, PhD Program Med Biotechnol, Taipei, Taiwan
来源
SCIENTIFIC REPORTS | 2018年 / 8卷
关键词
ZINC-FINGER PROTEINS; RNA-BINDING PROTEINS; SIGNAL-REGULATED KINASE; MESSENGER-RNAS; TRISTETRAPROLIN; TTP; ALPHA; DECAY; GENE; DIFFERENTIATION;
D O I
10.1038/s41598-018-21160-z
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
ZFP36 family members include ZFP36, ZFP36L1, and ZFP36L2, which belong to CCCH-type zinc finger proteins with two tandem zinc finger (TZF) regions. Whether ZFP36L1 and ZFP36L2 have antiproliferative activities similar to that of ZFP36 is unclear. In this study, when ZFP36L1 or ZFP36L2 was overexpressed in T-REx-293 cells, cell proliferation was dramatically inhibited and the cell cycle was arrested at the G1 phase. The levels of cell-cycle-related proteins, including cyclin B, cyclin D, cyclin A, and p21, decreased; however, p53 increased in ZFP36L1-or ZFP36L2-overexpressing T-REx-293 cells. Forced expression of ZFP36L1 or ZFP36L2 also inhibited cell proliferation and cyclin D gene expression in three human colorectal cancer cell lines: HCT116 p53(+/+), HCT116 p53(-/-), and SW620 (mutated p53) cells. However, it increased p53 and p21 expression only in HCT116 p53(+/+) cells. Knockdown of ZFP36L1 or ZFP36L2 increased cell proliferation and cyclin D expression; furthermore, the mutation of the TZF of ZFP36L1 or ZFP36L2 caused them to lose their antiproliferative ability, to the extent that they could not inhibit cyclin D expression in these three cell lines. The results indicated that ZFP36L1 and ZFP36L2 play a negative role in cell proliferation; the underlying mechanisms might be mediated through a cyclin D-dependent and p53-independent pathway.
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页数:13
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