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维生素D3上调蛋白1在肝癌发生过程中抑制肿瘤坏死因子-α诱导的核因子-κB激活。

Vitamin D3 upregulated protein 1 suppresses TNF-α-induced NF-κB activation in hepatocarcinogenesis.

作者信息

Kwon Hyo-Jung, Won Young-Suk, Suh Hyun-Woo, Jeon Jun-Ho, Shao Yan, Yoon Suk-Ran, Chung Jin-Woong, Kim Tae-Don, Kim Hwan-Mook, Nam Ki-Hoan, Yoon Won-Kee, Kim Dae-Ghon, Kim Jeong-Hwan, Kim Young-Sung, Kim Dae-Yong, Kim Hyoung-Chin, Choi Inpyo

机构信息

Bio-Evaluation Center, Korea Research Institute of Bioscience and Biotechnology, Chungbuk, South Korea.

出版信息

J Immunol. 2010 Oct 1;185(7):3980-9. doi: 10.4049/jimmunol.1000990. Epub 2010 Sep 8.

DOI:10.4049/jimmunol.1000990
PMID:20826751
Abstract

Vitamin D(3) upregulated protein 1 (VDUP1) is a candidate tumor suppressor, the expression of which is dramatically reduced in various tumor tissues. In this study, we found that VDUP1 expression is suppressed during human hepatic carcinogenesis, and mice lacking VDUP1 are much more susceptible to diethylnitrosamine-induced hepatocarcinogenesis compared with wild type mice. VDUP1-deficient tumors proliferated significantly more than wild type tumors and had corresponding changes in the expression of key cell cycle regulatory proteins. In addition, the hepatomitogen-induced response was associated with a considerable increase in the release of TNF-α and subsequent enhancement of NF-κB activation in VDUP1-deficient mice. When cells were treated with TNF-α, the VDUP1 level was markedly reduced, concomitant with elevated NF-κB activation. Furthermore, the overexpression of VDUP1 resulted in the robust suppression of TNF-α-activated NF-κB activity via association with HDAC1 and HDAC3. These results indicate that VDUP1 negatively regulates hepatocarcinogenesis by suppressing TNF-α-induced NF-κB activation.

摘要

维生素D(3)上调蛋白1(VDUP1)是一种候选肿瘤抑制因子,其在多种肿瘤组织中的表达显著降低。在本研究中,我们发现VDUP1的表达在人类肝癌发生过程中受到抑制,与野生型小鼠相比,缺乏VDUP1的小鼠对二乙基亚硝胺诱导的肝癌发生更敏感。缺乏VDUP1的肿瘤比野生型肿瘤增殖明显更多,并且关键细胞周期调节蛋白的表达有相应变化。此外,肝有丝分裂原诱导的反应与缺乏VDUP1的小鼠中TNF-α释放的显著增加以及随后NF-κB激活的增强有关。当细胞用TNF-α处理时,VDUP1水平显著降低,同时NF-κB激活升高。此外,VDUP1的过表达通过与HDAC1和HDAC3结合导致TNF-α激活的NF-κB活性受到强烈抑制。这些结果表明,VDUP1通过抑制TNF-α诱导的NF-κB激活对肝癌发生起负调节作用。

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