Expression and Post-translational Modification of Heat Shock Protein 27 (HSP27) in Cancer
Tomoko Oya‐Ito, Tomohisa Takagi, Keisuke Shima, Yuji Naito
Abstract
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Tomoko Oya‐Ito, Tomohisa Takagi, Keisuke Shima, Yuji Naito
Abstract
Open-access reader
Heat shock protein 27 (HSP27) is induced by heat shock, environmental, and pathophysiological stressors. HSP27 functions as a molecular chaperone and an anti-apoptotic protein in cells. Dynamic changes such as phosphorylation and oligomerization of HSP27 allow cells to adapt to changes in physiological functions and mount a protective response to damage. HSP27 is highly expressed in aggressive cancers, where it is involved in numerous pro-tumorigenic signaling pathways and is associated with poor prognosis and treatment resistant. This review focuses on the recent findings of the role of HSP27, particularly post-translational modification of HSP27 in cancer, and the strategies for therapeutic purposes by using HSP27 inhibitors.
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Heat shock protein 27 (HSP27) is induced by heat shock, environmental, and pathophysiological stressors. HSP27 functions as a molecular chaperone and an anti-apoptotic protein in cells. Dynamic changes such as phosphorylation and oligomerization of HSP27 allow cells to adapt to changes in physiological functions and mount a protective response to damage. HSP27 is highly expressed in aggressive cancers, where it is involved in numerous pro-tumorigenic signaling pathways and is associated with poor prognosis and treatment resistant. This review focuses on the recent findings of the role of HSP27, particularly post-translational modification of HSP27 in cancer, and the strategies for therapeutic purposes by using HSP27 inhibitors.
Key concepts: Hsp27, Heat shock protein, Phosphorylation, Cancer research, Cell biology, Biology, Chaperone (clinical), Posttranslational modification