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MDM2 as a Rational Target for Intervention in CDK4/6 Inhibitor Resistant, Hormone Receptor Positive Breast Cancer.
Portman, Neil; Chen, Julia; Lim, Elgene.
Affiliation
  • Portman N; Cancer Theme, Garvan Institute of Medical Research, Darlinghurst, NSW, Australia.
  • Chen J; St. Vincent's Clinical School, University of New South Wales (UNSW) Sydney, Kensington, NSW, Australia.
  • Lim E; Cancer Theme, Garvan Institute of Medical Research, Darlinghurst, NSW, Australia.
Front Oncol ; 11: 777867, 2021.
Article in En | MEDLINE | ID: mdl-34804982
ABSTRACT
With the adoption of inhibitors of cyclin dependent kinases 4 and 6 (CDK4/6i) in combination with endocrine therapy as standard of care for the treatment of advanced and metastatic estrogen receptor positive (ER+) breast cancer, the search is now on for novel therapeutic options to manage the disease after the inevitable development of resistance to CDK4/6i. In this review we will consider the integral role that the p53/MDM2 axis plays in the interactions between CDK4/6, ERα, and inhibitors of these molecules, the current preclinical evidence for the efficacy of MDM2 inhibitors in ER+ breast cancer, and discuss the possibility of targeting the p53/MDM2 via inhibition of MDM2 in the CDK4/6i resistance setting.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Front Oncol Year: 2021 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Front Oncol Year: 2021 Document type: Article Affiliation country: