Strategies to degrade estrogen receptor α in primary and ESR1 mutant-expressing metastatic breast cancer-Reference-Cited by-同舟云学术

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Strategies to degrade estrogen receptor α in primary and ESR1 mutant-expressing metastatic breast cancer

Published:2019-01 Issue: Volume:480 Page:107-121
ISSN:0303-7207
Container-title:Molecular and Cellular Endocrinology
language:en
Short-container-title:Molecular and Cellular Endocrinology

Author:

Busonero Claudia,Leone Stefano,Bartoloni Stefania,Acconcia Filippo^ORCID

Funder

Ateneo Roma Tre and Fondo di finanziamento per le attività base di ricerca (FFABR)

MIUR

University Roma

AIRC-Associazione Italiana Ricerca sul Cancro

Publisher

Elsevier BV

Subject

Endocrinology,Molecular Biology,Biochemistry

Reference134 articles.

1. The effects of 17beta-estradiol in cancer are mediated by estrogen receptor signaling at the plasma membrane;Acconcia;Front. Physiol.,2011

2. S-palmitoylation modulates human estrogen receptor-alpha functions;Acconcia;Biochem. Biophys. Res. Commun.,2004

3. Palmitoylation-dependent estrogen receptor alpha membrane localization: regulation by 17 beta-estradiol;Acconcia;Mol. Biol. Cell,2005

4. An inherent role of integrin-linked kinase-estrogen receptor alpha interaction in cell migration;Acconcia;Cancer Res.,2006

5. Xenoestrogen regulation of ERalpha/ERbeta balance in hormone-associated cancers;Acconcia;Mol. Cell. Endocrinol.,2016

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1. Selective impact of ALK and MELK inhibition on ERα stability and cell proliferation in cell lines representing distinct molecular phenotypes of breast cancer;Scientific Reports;2024-04-08

2. Pharmacological insights on novel oral selective estrogen receptor degraders in breast cancer;European Journal of Pharmacology;2024-04

3. PMM2 controls ERα levels and cell proliferation in ESR1 Y537S variant expressing breast cancer cells;Molecular and Cellular Endocrinology;2024-04

4. Selective Impact of ALK and MELK Inhibition on ERα Stability and Cell Proliferation in Cell Lines Representing Distinct Molecular Phenotypes of Breast Cancer;2023-12-19

5. X-ray crystallography study and optimization of novel benzothiophene analogs as potent selective estrogen receptor covalent antagonists (SERCAs) with improved potency and safety profiles;Bioorganic Chemistry;2023-12

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