Suppression of ABCG2 inhibits cancer cell proliferation

被引:52
作者
Chen, Zhong
Liu, Fang
Ren, Qian
Zhao, Qinjun
Ren, Hongying
Lu, Shihong
Zhang, Lei
Han, Zhongchao [1 ]
机构
[1] Chinese Acad Med Sci, Inst Hematol, State Key Lab Expt Hematol, Tianjin 300020, Peoples R China
基金
中国国家自然科学基金;
关键词
ABCG2; cell cycle; cyclin D3; p21; Cip1; RNA interference; proliferation; MULTIDRUG-RESISTANCE; BCRP/ABCG2; EXPRESSION; DRUG TRANSPORTER; SIDE-POPULATION; STEM-CELLS; IN-VITRO; PLUMBAGIN; VITAMIN-K3; ARREST; BCRP;
D O I
10.1002/ijc.24796
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The ATP-binding cassette efflux transporter, ABCG2, is widely expressed in a variety of normal tissues, stem cells, as well as cancer cells. Existing data suggest that ABCG2 plays an important role in the maintenance of the stem cell phenotype and multidrug resistance of cancer cells. However, the potential role of ABCG2 in other cellular processes remains speculative and poorly understood. Here, we demonstrated that ABCG2 is involved in the proliferation of cancer cells. We used RNA interference approach to efficiently and specifically down-regulate ABCG2 protein levels in MCF-7/MX and A549 cells. We showed that knockdown of ABCG2 significantly inhibited the proliferation of these cells. Suppression of ABCG2 reduced the percentage of cells in the S phase of the cell cycle and enhanced G0/G1 accumulation. The G0/G1 growth arrest was associated with down-regulation of cyclin D3 and up-regulation of p21. Furthermore, blocking of ABCG2 function by chemical inhibitor fumitremorgin C also inhibited cell proliferation via the prolonged G0/G1 interval. Taken together, these findings suggest that ABCG2 correlates with cell cycle progression, highlighting a novel function of ABCG2 in cancer cell proliferation.
引用
收藏
页码:841 / 851
页数:11
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