Journal
CANCER LETTERS
Volume 385, Issue -, Pages 75-86Publisher
ELSEVIER IRELAND LTD
DOI: 10.1016/j.canlet.2016.10.045
Keywords
Doxorubicin; Hsp60; Acetylation; Ubiquitination; p53; Replicative senescence
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Funding
- Italian National Operational Programme for Research and Competitiveness [PONa3_00210]
- IMET
- IEMEST
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The chaperone Hsp60 is pro-carcinogenic in certain tumor types by interfering with apoptosis and with tumor cell death. In these tumors, it is not yet known whether doxorubicin anti-tumor effects include a blockage of the pro-carcinogenic action of Hsp60. We found a doxorubicin dose-dependent viability reduction in a human lung mucoepidermoid cell line that was paralleled by the appearance of cell senescence markers. Concomitantly, intracellular Hsp60 levels decreased while its acetylation levels increased. The data suggest that Hsp60 acetylation interferes with the formation of the Hsp60/p53 complex and/or promote its dissociation, both causing an increase in the levels of free p53, which can then activate the p53-dependent pathway toward cell senescence. On the other hand, acetylated Hsp60 is ubiquitinated and degraded and, thus, the anti-apoptotic effect of the chaperonin is abolished with subsequent tumor cell death. Our findings could help in the elucidation of the molecular mechanisms by which doxorubicin counteracts carcinogenesis and, consequently, it would open new roads for the development of cancer treatment protocols targeting Hsp60. (C) 2016 Elsevier Ireland Ltd. All rights reserved.
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