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核因子κB和活化蛋白-1参与人乳头瘤病毒16型E5癌蛋白上调环氧化酶-2的过程。

Involvement of NF-kappaB and AP-1 in COX-2 upregulation by human papillomavirus 16 E5 oncoprotein.

作者信息

Kim Su-Hyeong, Oh Jung-Min, No Jae-Hong, Bang Yung-Jue, Juhnn Yong-Sung, Song Yong-Sang

机构信息

Cancer Research Institute, Seoul National University College of Medicine, 28 Yongon-Dong, Chongno-Ku, Seoul 110-744, Korea.

出版信息

Carcinogenesis. 2009 May;30(5):753-7. doi: 10.1093/carcin/bgp066. Epub 2009 Mar 25.

Abstract

The human papillomavirus (HPV) E6 and E7 oncoproteins play important roles in cervical carcinogenesis through multiple mechanisms, including upregulation of cyclooxygenase-2 (COX-2), which has been shown to be involved in both carcinogenesis and cancer progression. To explore the role of E5 in cervical carcinogenesis, we herein investigated the effect of HPV 16 E5 on COX-2 expression. Our results revealed that E5 induced COX-2 expression through the epidermal growth factor receptor-signaling pathway, with nuclear factor-kappaB (NF-kappaB) and activator protein-1 (AP-1) acting as critical factors in E5-induced COX-2 expression. NF-kappaB inhibition blocked COX-2 expression more potently than inhibition of AP-1. Our findings collectively suggest that the HPV 16 E5 oncoprotein mediates cervical carcinogenesis at least in part via upregulation of COX-2 expression through NF-kappaB and AP-1, with NF-kappaB playing a larger role.

摘要

人乳头瘤病毒(HPV)E6和E7癌蛋白通过多种机制在宫颈癌发生过程中发挥重要作用,包括上调环氧合酶-2(COX-2),已有研究表明COX-2参与致癌作用和癌症进展。为了探究E5在宫颈癌发生中的作用,我们在此研究了HPV 16 E5对COX-2表达的影响。我们的结果显示,E5通过表皮生长因子受体信号通路诱导COX-2表达,其中核因子-κB(NF-κB)和活化蛋白-1(AP-1)是E5诱导COX-2表达的关键因子。抑制NF-κB比抑制AP-1更有效地阻断COX-2表达。我们的研究结果共同表明,HPV 16 E5癌蛋白至少部分通过NF-κB和AP-1上调COX-2表达来介导宫颈癌发生,其中NF-κB发挥更大作用。

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