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BCL-2 protein family: attractive targets for cancer therapy.
Kaloni, Deeksha; Diepstraten, Sarah T; Strasser, Andreas; Kelly, Gemma L.
Affiliation
  • Kaloni D; Blood Cells and Blood Cancer Division, Walter and Eliza Hall Institute of Medical Research, Melbourne, VIC, Australia.
  • Diepstraten ST; Department of Medical Biology, University of Melbourne, Melbourne, VIC, Australia.
  • Strasser A; Blood Cells and Blood Cancer Division, Walter and Eliza Hall Institute of Medical Research, Melbourne, VIC, Australia.
  • Kelly GL; Blood Cells and Blood Cancer Division, Walter and Eliza Hall Institute of Medical Research, Melbourne, VIC, Australia.
Apoptosis ; 28(1-2): 20-38, 2023 Feb.
Article in En | MEDLINE | ID: mdl-36342579
ABSTRACT
Acquired resistance to cell death is a hallmark of cancer. The BCL-2 protein family members play important roles in controlling apoptotic cell death. Abnormal over-expression of pro-survival BCL-2 family members or abnormal reduction of pro-apoptotic BCL-2 family proteins, both resulting in the inhibition of apoptosis, are frequently detected in diverse malignancies. The critical role of the pro-survival and pro-apoptotic BCL-2 family proteins in the regulation of apoptosis makes them attractive targets for the development of agents for the treatment of cancer. This review describes the roles of the various pro-survival and pro-apoptotic members of the BCL-2 protein family in normal development and organismal function and how defects in the control of apoptosis promote the development and therapy resistance of cancer. Finally, we discuss the development of inhibitors of pro-survival BCL-2 proteins, termed BH3-mimetic drugs, as novel agents for cancer therapy.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Apoptosis / Neoplasms Limits: Humans Language: En Journal: Apoptosis Year: 2023 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Apoptosis / Neoplasms Limits: Humans Language: En Journal: Apoptosis Year: 2023 Document type: Article Affiliation country: