MedElevator Войти в исследования
← Поиск публикаций

DOI 10.3389/fonc.2021.759577

Медицинская библиотека · Frontiers in oncology · 2021

ARID1A Mutation in Metastatic Breast Cancer: A Potential Therapeutic Target.

Cheng Xuan, Zhao Jian-Xiong, Dong Feng, Cao Xu-Chen

СтатьяОбзорПеревод в очереди

Аннотация

Distant metastasis is the principal cause of mortality for breast cancer patients. Targeting specific mutations that have been acquired during the evolution process of advanced breast cancer is a potential means of enhancing the clinical efficacy of treatment strategies. In metastatic breast cancer, ARID1A is the most prevalent mutation of the SWI/SNF complex, which regulates DNA repair, recombination, and gene transcription. The low expression of ARID1A is associated with poor disease-free survival and overall survival of patients with luminal A or HER2-rich breast cancer. In addition, ARID1A plays a prominent role in maintaining luminal characteristics and has an advantage for identifying responses to treatment, including endocrine therapies, HDAC inhibitors and CDK4/6 inhibitors. The therapeutic vulnerabilities initiated by ARID1A alterations encourage us to explore new approaches to cope with ARID1A mutant-related drug resistance or metastasis. In this review, we describe the mutation profiles of ARID1A in metastatic breast cancer and the structure and function of ARID1A and the SWI/SNF complex as well as discuss the potential mechanisms of ARID1A-mediated endocrine resistance and therapeutic potential.

Для цитирования: Cheng Xuan, Zhao Jian-Xiong, Dong Feng, Cao Xu-Chen. ARID1A Mutation in Metastatic Breast Cancer: A Potential Therapeutic Target.. Frontiers in oncology. 2021. DOI: 10.3389/fonc.2021.759577.
Подготовка и перевод публикации
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…

История · было → стало

Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.

Тип публикации указан по данным источника. Уровень доказательности автоматически не присваивается.