CYR61 controls p53 and NF-κB expression through PI3K/Akt/mTOR pathways in carboplatin-induced ovarian cancer cells

被引:69
|
作者
Lee, Kwang-Beom [2 ]
Byun, Hyun-Jung [1 ]
Park, Sung Ho [3 ]
Park, Chan-Yong [2 ]
Lee, Seung-Hoon [4 ]
Rho, Seung Bae [1 ]
机构
[1] Natl Canc Ctr, Res Inst, Goyang Si 410769, Gyeonggi Do, South Korea
[2] Gachon Univ, Gil Hosp, Dept Obstet & Gynecol, Inchen 405760, South Korea
[3] Hallym Univ, Dept Obstet & Gynecol, Seoul 150950, South Korea
[4] Yong In Univ, Dept Life Sci, Yongin 449714, Gyeonggi Do, South Korea
关键词
CCN1 (CYR61); Apoptosis; Carboplatin; NF-kappa B; PI3K/Akt; Ovarian carcinoma cells; IMMEDIATE-EARLY GENE; CCN FAMILY; BREAST-CANCER; ENDOMETRIAL CANCER; TUMOR-SUPPRESSOR; APOPTOSIS; INHIBITION; GROWTH; BCL-2; PROLIFERATION;
D O I
10.1016/j.canlet.2011.10.016
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
CYR61 over-expression promotes cell proliferation by inhibiting carboplatin-induced apoptosis, decreasing Bax expression, and increasing Bcl-xL, Mcl-1, and Bcl-2. At the same time, down-regulating p53 expression, while up-regulated NF-kappa B expression. Additionally, p21 and p53 promoter activities were reduced, while NF-kappa B and Bcl-2 activities increased. In parallel, CYR61-expressing cells, during carboplatin-induced apoptosis, resulted in an increase of Akt phosphorylation, while rapamycin-treated cells were not affected. Carboplatin effectively inhibited the activation of mTOR signaling cascade, which includes mTOR, 4E-BP1, p70S6K, HIF-1 alpha, and VEGF. These results provide evidence that CYR61 promotes cell proliferation and inhibits apoptosis. (C) 2011 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:86 / 95
页数:10
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