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CYR61 通过 PI3K/Akt/mTOR 通路调控顺铂诱导的卵巢癌细胞中 p53 和 NF-κB 的表达。

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

机构信息

Department of Obstetrics and Gynecology, Gachon University Gil Hospital, Guwol-Dong, Namdong-Gu, Inchen, Republic of Korea.

出版信息

Cancer Lett. 2012 Feb 1;315(1):86-95. doi: 10.1016/j.canlet.2011.10.016. Epub 2011 Oct 21.

Abstract

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-κB expression. Additionally, p21 and p53 promoter activities were reduced, while NF-κB 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-1α, and VEGF. These results provide evidence that CYR61 promotes cell proliferation and inhibits apoptosis.

摘要

CYR61 过表达通过抑制卡铂诱导的细胞凋亡、降低 Bax 表达、增加 Bcl-xL、Mcl-1 和 Bcl-2 来促进细胞增殖。同时,下调 p53 表达,而上调 NF-κB 表达。此外,p21 和 p53 启动子活性降低,而 NF-κB 和 Bcl-2 活性增加。平行地,在卡铂诱导的细胞凋亡过程中,表达 CYR61 的细胞导致 Akt 磷酸化增加,而雷帕霉素处理的细胞不受影响。卡铂有效地抑制了 mTOR 信号级联的激活,包括 mTOR、4E-BP1、p70S6K、HIF-1α 和 VEGF。这些结果提供了证据表明 CYR61 促进细胞增殖并抑制细胞凋亡。

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