Literature DB >> 18477563

Phosphorylated heat shock protein 27 represses growth of hepatocellular carcinoma via inhibition of extracellular signal-regulated kinase.

Rie Matsushima-Nishiwaki1, Shinji Takai, Seiji Adachi, Chiho Minamitani, Eisuke Yasuda, Takahiro Noda, Kanefusa Kato, Hidenori Toyoda, Yuji Kaneoka, Akihiro Yamaguchi, Takashi Kumada, Osamu Kozawa.   

Abstract

Heat shock protein 27, one of the low molecular weight stress proteins, is recognized as a molecular chaperone; however, other functions have not yet been well established. Phosphorylated heat shock protein 27 levels inversely correlate with the progression of human hepatocellular carcinoma. This study shows that phosphorylated heat shock protein 27 interferes with cell growth of the hepatocellular carcinoma-derived HuH7 cells in the presence of the proinflammatory cytokine, tumor necrosis factor-alpha, via inhibition of the sustained activation of the extracellular signal-regulated kinase signal pathway. The activities of Raf/extracellular signal-regulated kinase and subsequent activator protein-1 transactivation and the induction levels of cyclin D1 were lower in HuH7 cells transfected with phosphorylated heat shock protein 27 than those with unphosphorylated heat shock protein 27. Moreover, phosphorylated heat shock protein 27 up-regulated the levels of p38 mitogen-activated protein kinase and mitogen-activated protein kinase phosphatase-1, an inhibitory protein of extracellular signal-regulated kinase. These results indicate that phosphorylated heat shock protein 27 might suppress the extracellular signal-regulated kinase activity in the hepatocellular carcinoma cells via two separate pathways in an inflammatory state. The extracellular signal-regulated kinase activity is inversely correlated with phosphorylated heat shock protein 27 at serine 15 and also in human hepatocellular carcinoma tissues in vivo. Because the extracellular signal-regulated kinase signal pathway is a major proliferation signal of hepatocellular carcinoma, activator protein-1 activation is an early event in hepatocarcinogenesis. These findings strongly suggest that the control of the phosphorylated heat shock protein 27 levels could be a new therapeutic strategy especially to counter the recurrence of hepatocellular carcinoma.

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Year:  2008        PMID: 18477563     DOI: 10.1074/jbc.M801301200

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  12 in total

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Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  2011-10-20       Impact factor: 3.000

Review 2.  Heat shock protein 27 phosphorylation: kinases, phosphatases, functions and pathology.

Authors:  Sergiy Kostenko; Ugo Moens
Journal:  Cell Mol Life Sci       Date:  2009-07-11       Impact factor: 9.261

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Journal:  Cell Mol Life Sci       Date:  2015-07-27       Impact factor: 9.261

4.  Inhibition of protein phosphorylation in MIA pancreatic cancer cells: confluence of metabolic and signaling pathways.

Authors:  Hengwei Zhang; Rui Cao; Wai-Nang Paul Lee; Caishu Deng; Yingchun Zhao; Joan Lappe; Robert Recker; Yun Yen; Qi Wang; Ming-Ying Tsai; Vay Liang Go; Gary Guishan Xiao
Journal:  J Proteome Res       Date:  2010-02-05       Impact factor: 4.466

5.  Heat shock response associated with hepatocarcinogenesis in a murine model of hereditary tyrosinemia type I.

Authors:  Francesca Angileri; Geneviève Morrow; Vincent Roy; Diana Orejuela; Robert M Tanguay
Journal:  Cancers (Basel)       Date:  2014-04-23       Impact factor: 6.639

Review 6.  Heat shock protein 27 phosphorylation state is associated with cancer progression.

Authors:  Maria Katsogiannou; Claudia Andrieu; Palma Rocchi
Journal:  Front Genet       Date:  2014-10-06       Impact factor: 4.599

7.  The significance of phosphorylated heat shock protein 27 on the prognosis of pancreatic cancer.

Authors:  Mitsuru Okuno; Ichiro Yasuda; Seiji Adachi; Masanori Nakashima; Junji Kawaguchi; Shinpei Doi; Takuji Iwashita; Yoshinobu Hirose; Osamu Kozawa; Naoki Yoshimi; Masahito Shimizu; Hisataka Moriwaki
Journal:  Oncotarget       Date:  2016-03-22

8.  ZNF322A-mediated protein phosphorylation induces autophagosome formation through modulation of IRS1-AKT glucose uptake and HSP-elicited UPR in lung cancer.

Authors:  Chantal Hoi Yin Cheung; Chia-Lang Hsu; Tsai-Yu Lin; Wei-Ting Chen; Yi-Ching Wang; Hsuan-Cheng Huang; Hsueh-Fen Juan
Journal:  J Biomed Sci       Date:  2020-06-23       Impact factor: 8.410

9.  Network-Based Analysis of Nutraceuticals in Human Hepatocellular Carcinomas Reveals Mechanisms of Chemopreventive Action.

Authors:  M Michailidou; I N Melas; D E Messinis; S Klamt; L G Alexopoulos; F N Kolisis; H Loutrari
Journal:  CPT Pharmacometrics Syst Pharmacol       Date:  2015-06-01

Review 10.  The Clinical Significance of Phosphorylated Heat Shock Protein 27 (HSPB1) in Pancreatic Cancer.

Authors:  Mitsuru Okuno; Seiji Adachi; Osamu Kozawa; Masahito Shimizu; Ichiro Yasuda
Journal:  Int J Mol Sci       Date:  2016-01-21       Impact factor: 5.923

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