4.7 Article

Caveolin-1 regulates Mcl-1 stability and anoikis in lung carcinoma cells

期刊

AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY
卷 302, 期 9, 页码 C1284-C1292

出版社

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajpcell.00318.2011

关键词

lung cancer; anoikis resistance; metastasis; myeloid cell leukemia-1

资金

  1. Higher Education Research Promotion
  2. National Research University, Chulalongkorn University
  3. National Institutes of Health [R01-HL076340-04S1]

向作者/读者索取更多资源

Chunhacha P, Pongrakhananon V, Rojanasakul Y, Chanvorachote P. Caveolin-1 regulates Mcl-1 stability and anoikis in lung carcinoma cells. Am J Physiol Cell Physiol 302: C1284-C1292, 2012. First published January 25, 2012; doi:10.1152/ajpcell.00318.2011.-Both caveolin-1 (Cav-1) and Mcl-1 have been implicated in the regulation of cancer cell anoikis, but their relationship and underlying mechanisms of regulation are not known. The present study demonstrated for the first time that Cav-1 regulates Mcl-1 through protein-protein interaction and inhibits its downregulation during cell anoikis in human lung cancer cells. Immunoprecipitation and immunocytochemistry studies showed that Cav-1 interacted with Mcl-1 and prevented it from degradation via the ubiquitin-proteasome pathway. Mcl-1 and Mcl-1-Cav-1 complex were highly elevated in Cav-1-overexpressing cells but were greatly reduced in Cav-1 knockdown cells. Consistent with this finding, we found that Mcl-1 ubiquitination was significantly attenuated by Cav-1 overexpression but increased by Cav-1 knockdown. Together, our results indicate a novel role of Cav-1 in anoikis regulation through Mcl-1 interaction and stabilization, which provides a new insight to the pathogenesis of metastatic lung cancer and its potential treatment.

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