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Epigenetic mechanisms of cancer progression and therapy resistance in estrogen-receptor (ER+) breast cancer.
Toska, Eneda.
Afiliação
  • Toska E; Sidney Kimmel Comprehensive Cancer Center and Department of Oncology, Johns Hopkins University, Baltimore, MD, USA; Department of Biochemistry and Molecular Biology, Johns Hopkins School of Public Health, Baltimore, MD, USA. Electronic address: etoska1@jhmi.edu.
Biochim Biophys Acta Rev Cancer ; 1879(3): 189097, 2024 May.
Article em En | MEDLINE | ID: mdl-38518961
ABSTRACT
Estrogen receptor-positive (ER+) breast cancer is the most frequent breast cancer subtype. Agents targeting the ER signaling pathway have been successful in reducing mortality from breast cancer for decades. However, mechanisms of resistance to these treatments arise, especially in the metastatic setting. Recently, it has been recognized that epigenetic dysregulation is a common feature that facilitates the acquisition of cancer hallmarks across cancer types, including ER+ breast cancer. Alterations in epigenetic regulators and transcription factors (TF) coupled with changes to the chromatin landscape have been found to orchestrate breast oncogenesis, metastasis, and the development of a resistant phenotype. Here, we review recent advances in our understanding of how the epigenome dictates breast cancer tumorigenesis and resistance to targeted therapies and discuss novel therapeutic interventions for overcoming resistance.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Receptores de Estrogênio / Resistencia a Medicamentos Antineoplásicos / Epigênese Genética Limite: Animals / Female / Humans Idioma: En Revista: Biochim Biophys Acta Rev Cancer Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Receptores de Estrogênio / Resistencia a Medicamentos Antineoplásicos / Epigênese Genética Limite: Animals / Female / Humans Idioma: En Revista: Biochim Biophys Acta Rev Cancer Ano de publicação: 2024 Tipo de documento: Article