Targeting the Estrogen Receptor for the Treatment of Breast Cancer: Recent Advances and Challenges.


Journal

Journal of medicinal chemistry
ISSN: 1520-4804
Titre abrégé: J Med Chem
Pays: United States
ID NLM: 9716531

Informations de publication

Date de publication:
13 07 2023
Historique:
medline: 14 7 2023
pubmed: 28 6 2023
entrez: 28 6 2023
Statut: ppublish

Résumé

Estrogen receptor alpha (ERα) is a well-established therapeutic target for the treatment of ER-positive (ER+) breast cancers. Despite the tremendous successes achieved with tamoxifen, a selective ER modulator, and aromatase inhibitors (AIs), resistance to these therapies is a major clinical problem. Therefore, induced protein degradation and covalent inhibition have been pursued as new therapeutic approaches to target ERα. This Perspective summarizes recent progress in the discovery and development of oral selective ER degraders (SERDs), complete estrogen receptor antagonists (CERANs), selective estrogen receptor covalent antagonists (SERCAs), and proteolysis targeting chimera (PROTAC) ER degraders. We focus on those compounds which have been advanced into clinical development.

Identifiants

pubmed: 37377342
doi: 10.1021/acs.jmedchem.3c00136
doi:

Substances chimiques

Receptors, Estrogen 0
Estrogen Receptor alpha 0
Tamoxifen 094ZI81Y45
Aromatase Inhibitors 0
Selective Estrogen Receptor Modulators 0
Estrogen Antagonists 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

8339-8381

Auteurs

Rohan Kalyan Rej (RK)

Rogel Cancer Center, University of Michigan, Ann Arbor, Michigan 48109, United States.
Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan 48109, United States.

Junius Eugene Thomas (JE)

Rogel Cancer Center, University of Michigan, Ann Arbor, Michigan 48109, United States.
Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan 48109, United States.
Program in Chemical Biology, University of Michigan, Ann Arbor, Michigan 48109, United States.

Ranjan Kumar Acharyya (RK)

Rogel Cancer Center, University of Michigan, Ann Arbor, Michigan 48109, United States.
Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan 48109, United States.

James Michael Rae (JM)

Rogel Cancer Center, University of Michigan, Ann Arbor, Michigan 48109, United States.
Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan 48109, United States.
Department of Pharmacology, University of Michigan, Ann Arbor, Michigan 48109, United States.

Shaomeng Wang (S)

Rogel Cancer Center, University of Michigan, Ann Arbor, Michigan 48109, United States.
Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan 48109, United States.
Department of Pharmacology, University of Michigan, Ann Arbor, Michigan 48109, United States.
Department of Medicinal Chemistry, University of Michigan, Ann Arbor, Michigan 48109, United States.
Program in Chemical Biology, University of Michigan, Ann Arbor, Michigan 48109, United States.

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Classifications MeSH