Heat Shock Protein 27 (HSP27, HSPB1) Is Up-Regulated by Targeted Agents and Confers Resistance to Both Targeted Drugs and Chemotherapeutics

作者: Daniele Musiani , John David Konda , Simona Pavan , Erica Torchiaro , Jessica Erriquez

DOI: 10.1007/978-3-319-17211-8_2

关键词:

摘要: The Heat Shock Protein of 27 kDa (HSP27) is a molecular chaperone with anti-apoptotic properties and role in cytoskeleton stability. Not surprisingly, HSP27 often increased cancers associated poor patients’ survival resistance to conventional chemotherapy. Conversely, the response therapies targeted towards oncogenic kinases was poorly characterized. In this chapter we review findings on both chemotherapeutics drugs pro-metastatic phenotype, focusing where tyrosine kinase receptor encoded by MET oncogene activated, namely, gastric ovarian cancers. inhibition addicted cancer cells triggered increase MEK/ERK dependent manner turn limited effectiveness inhibitors vitro vivo. Furthermore, required for metastasis upon activation vivo modulates sensitivity first line Cisplatin Paclitaxel. Altogether, these suggested that induction agents might impact success it be suitable therapeutic target combination treatments.

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