HSP27 and HSP70: Potentially Oncogenic Apoptosis Inhibitors
Article 2003 en
Authors
CG
Carmen Garrido
ES
E. Schmitt
CC
Céline Candé
Abstract
1 min read
Stress or heat shock proteins (HSPs) such as HSP27 and HSP70 are expressed in response to a wide variety of physiological and environmental insults including heat, reactive oxygen species or anticancer drugs. Their overexpression allows cells to survive to otherwise lethal conditions. Several different mechanisms may account for the cytoprotective activity of HSP27 and HSP70. First, both proteins are powerful chaperones. Second, both inhibit key effectors of the apoptotic machinery including the apoptosome, the caspase activation complex (both HSP27 and HSP70), and apoptosis inducing factor (only HSP70). Third, they both play a role in the proteasome-mediated degradation of apoptosis-regulatory proteins. HSP27 and HSP70 may participate in oncogenesis, as suggested by the fact that overexpression of heat shock proteins can increase the tumorigenic potential of tumor cells. The down-regulation or selective inhibition of HSP70 might constitute a valuable strategy for the treatment of cancer.
Elaine Hau Jin Yew, Nam Sang Cheung, M.S. Choy, Robert Z. Qi, Alan Yiu Wah Lee, Peng Zhao, Alirio J. Melendez, J. Manikandan, Evelyn S. C. Koay, Lily‐Lily Chiu, Wooi Loon Ng, Matthew Whiteman, Kandiah Jeyaseelan, Barry Halliwell
Anne-Laure Rérole, Jessica Gobbo, Aurélie de Thonel, E. Schmitt, Jean-Paul Paı̈s de Barros, Arlette Hammann, David Lanneau, Eric Fourmaux, Oleg Deminov, Olivier Micheau, Laurent Lagrost, Pierre Colas, Guido Guido Kroemer, Carmen Garrido
Anne-Laure Rérole, Jessica Gobbo, Aurelie De Thonel, E. Schmitt, Jean-Paul Paı̈s de Barros, Arlette Hammann, David Lanneau, Eric Fourmaux, Oleg Deminov, Olivier Micheau, Laurent Lagrost, Pierre Colas, Guido Guido Kroemer, Carmen Garrido
Discussion(0)
No comments yet. Be the first to comment.