Endoplasmic reticulum stress stimulates the expression of cyclooxygenase-2 through activation of NF-κB and pp38 mitogen-activated protein kinase

Jui Hsiang Hung, Ih Jen Su, Huan Yao Lei, Hui Ching Wang, Wan Chi Lin, Wen Tsan Chang, Wenya Huang, Wen Chang Chang, Yung Sheng Chang, Ching Chow Chen, Ming Derg Lai

研究成果: 雜誌貢獻文章同行評審

194 引文 斯高帕斯(Scopus)

摘要

Expression of mutant proteins or viral infection may interfere with proper protein folding activity in the endoplasmic reticulum (ER). Several pathways that maintain cellular homeostasis were activated in response to these ER disturbances. Here we investigated which of these ER stress-activated pathways induce COX-2 and potentially oncogenesis. Tunicamycin and brefeldin A, two ER stress inducers, increased the expression of COX-2 in ML-1 or MCF-7 cells. Nuclear translocation of NF-κB and activation of pp38 MAPK were observed during ER stress. IκBα kinase inhibitor Bay 11-7082 or IkBα kinase dominant negative mutant significantly inhibited the induction of COX-2. pp38 MAPK inhibitor SB203580 or eIF2α phosphorylation inhibitor 2-aminopurine attenuated the nuclear NF-κB DNA binding activity and COX-2 induction. Expression of mutant hepatitis B virus (HBV) large surface proteins, inducers of ER stress, enhanced the expression of COX-2 in ML-1 and HuH-7 cells. Transgenic mice showed higher expression of COX-2 protein in liver and kidney tissue expressing mutant HBV large surface protein in vivo. Similarly, increased expression of COX-2 mRNA was observed in human hepatocellular carcinoma tissue expressing mutant HBV large surface proteins. In ML-1 cells expressing mutant HBV large surface protein, anchorage-independent growth was enhanced, and the enhancement was abolished by the addition of specific COX-2 inhibitors. Thus, ER stress due either to expression of viral surface proteins or drugs can stimulate the expression of COX-2 through the NF-κB and pp38 kinase pathways. Our results provide important insights into cellular carcinogenesis associated with latent endoplasmic reticulum stress.

原文英語
頁(從 - 到)46384-46392
頁數9
期刊Journal of Biological Chemistry
279
發行號45
DOIs
出版狀態已發佈 - 十一月 5 2004

ASJC Scopus subject areas

  • 生物化學
  • 分子生物學
  • 細胞生物學

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