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Androgen receptor: Structure, signaling, function and potential drug discovery biomarker in different breast cancer subtypes

雄激素受体 乳腺癌 前列腺癌 医学 癌症 恶性肿瘤 肿瘤科 癌变 生物标志物 内科学 癌症研究 生物信息学 生物 生物化学
作者
Nirali Shukla,Kunal Shah,Deepshikha Rathore,Kinal Soni,Jigna Shah,Hemangini H. Vora,Heena Dave
出处
期刊:Life Sciences [Elsevier]
卷期号:348: 122697-122697
标识
DOI:10.1016/j.lfs.2024.122697
摘要

The Androgen Receptor (AR) is emerging as an important factor in the pathogenesis of breast cancer (BC), which is the most common malignancy worldwide. >70 % of AR expression in primary and metastatic breast tumors has been observed which suggests that AR may be a new marker and a potential therapeutic target among AR-positive BC patients. Biological insight into AR-positive breast cancer reveals that AR may cross-talk with several vital signaling pathways, including key molecules and receptors. Downstream signaling of AR might also affect many clinically important pathways that are emerging as clinical targets in BC. AR exhibits different behaviors depending on the breast cancer molecular subtype. Preliminary clinical research using AR-targeted drugs, which have already been FDA-approved for prostate cancer (PC), has given promising results for AR-positive breast cancer patients. However, since AR positivity's prognostic and predictive value remains uncertain, it is difficult to identify and stratify patients who would benefit from AR-targeted therapies alone. Thus, the need of the hour is to target the androgen receptor as a monotherapy or in combination with other conventional therapies which has proven to be an effective clinical strategy for the treatment of prostate cancer patients, and these therapeutic strategies are increasingly being investigated in breast cancer. Therefore, in this manuscript, we review the role of AR in various cellular processes that promote tumorigenesis and aggressiveness, in different subtypes of breast cancer, as well as discuss ongoing efforts to target AR for the more effective treatment and prevention of breast cancer.
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