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过氧化物酶体增殖物激活受体γ配体15-脱氧-Δ12,14-前列腺素J2调节胆管癌细胞中凋亡相关蛋白的表达。

The PPARgamma ligand, 15-Deoxy-Delta12,14-PGJ2, regulates apoptosis-related protein expression in cholangio cell carcinoma cells.

作者信息

Okano Hiroshi, Shiraki Katsuya, Inoue Hidekazu, Kawakita Tomoyuki, Deguchi Masatoshi, Sugimoto Kazushi, Sakai Takahisa, Murata Kazumoto, Nakano Takeshi, Enjoji Munechika

机构信息

First Department of Internal Medicine, Mie University School of Medicine, 2-174 Edobashi, Tsu, Mie 514-8507, Japan.

出版信息

Int J Mol Med. 2003 Dec;12(6):867-70.

Abstract

PPARgamma is known to induce apoptosis in malignant tumor cells, but the mechanism of this induction is not well understood. We investigated induction of apoptosis with 15-Deoxy-Delta12,14-prostaglandin J2 (15d-PGJ2), a PPARgamma ligand, in cholangio cell carcinoma (CCC) cells (RBE, ETK-1 or HuCCT-1). Apoptosis was induced in RBE and ETK-1 cells with 15d-PGJ2, but not in HuCCT-1 cells, although PPARgamma was expressed in all CCC cells. Apoptosis-related proteins were also expressed, including FLIP, bclx, Apaf-1 and XIAP, but expression levels differed among the three cell lines. RBE cells treated with 15d-PGJ2 showed caspase activation, and it appeared that PPARgamma-induced apoptosis was dependent on caspase activation. However, neither ETK-1 nor HuCCT-1 cells showed significant activation of caspase-8 or -3 with 15d-PGJ2 treatment, raising the possibility of a caspase-independent apoptosis induction pathway. XIAP was down-regulated by 15d-PGJ2 in all three CCC cell lines. Therefore, 15d-PGJ2 induces apoptosis in CCC cells via caspase-dependent or independent pathways. 15d-PGJ2 may also induce down-regulation of XIAP and may promote caspase cascade activation through TNF-family receptor signaling pathways.

摘要

已知过氧化物酶体增殖物激活受体γ(PPARγ)可诱导恶性肿瘤细胞凋亡,但其诱导机制尚不清楚。我们研究了PPARγ配体15-脱氧-Δ12,14-前列腺素J2(15d-PGJ2)对胆管癌细胞(CCC,RBE、ETK-1或HuCCT-1细胞系)凋亡的诱导作用。15d-PGJ2可诱导RBE和ETK-1细胞凋亡,但不能诱导HuCCT-1细胞凋亡,尽管所有CCC细胞系均表达PPARγ。凋亡相关蛋白也有表达,包括FLIP、bclx、凋亡蛋白酶激活因子-1(Apaf-1)和X连锁凋亡抑制蛋白(XIAP),但三种细胞系中的表达水平有所不同。用15d-PGJ2处理的RBE细胞显示出半胱天冬酶激活,似乎PPARγ诱导的凋亡依赖于半胱天冬酶激活。然而,用15d-PGJ2处理ETK-1和HuCCT-1细胞均未显示半胱天冬酶-8或-3的显著激活,这增加了存在不依赖半胱天冬酶的凋亡诱导途径的可能性。在所有三种CCC细胞系中,15d-PGJ2均可使XIAP下调。因此,15d-PGJ2通过依赖或不依赖半胱天冬酶的途径诱导CCC细胞凋亡。15d-PGJ2还可能诱导XIAP下调,并可能通过肿瘤坏死因子家族受体信号通路促进半胱天冬酶级联激活。

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