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雄激素受体在三阴性乳腺癌中的研究进展:从分子机制到临床应用

Advances of androgen receptor in triple-negative breast cancer: from molecular mechanisms to clinical applications.

作者信息

Ma Lange, Xu Hao, Wang Chunyan, Hu Yue, Ren Qinglan, Yu Shengnan

机构信息

Department of Oncology, Laboratory of Immunity, Inflammation & Cancer, The First Affiliated Hospital of Chongqing Medical University, Chongqing, 400016, China.

出版信息

Discov Oncol. 2025 Sep 3;16(1):1677. doi: 10.1007/s12672-025-03431-0.


DOI:10.1007/s12672-025-03431-0
PMID:40897935
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12405098/
Abstract

Triple-negative breast cancer (TNBC) is a clinically aggressive malignancy with high heterogeneity at molecular and genetic levels, which characterized by the absence of effective therapeutic targets and marked resistance to conventional chemotherapy regimens. The androgen receptor (AR) is highly expressed by TNBC tumor cells and plays a vital role on tumor progression. With more research into AR signaling pathways and functions, AR-targeted therapy is becoming a promising treatment strategy. This review synthesizes emerging evidence in AR-related preclinical research and clinical outcomes, including monotherapy and combined strategies based on AR-targeted treatment. Through the comprehensive review, we hope to find novel therapeutic insights for TNBC.

摘要

三阴性乳腺癌(TNBC)是一种临床侵袭性恶性肿瘤,在分子和基因水平上具有高度异质性,其特点是缺乏有效的治疗靶点且对传统化疗方案具有明显抗性。雄激素受体(AR)在TNBC肿瘤细胞中高表达,并在肿瘤进展中起关键作用。随着对AR信号通路和功能的研究不断深入,AR靶向治疗正成为一种有前景的治疗策略。本综述综合了AR相关临床前研究和临床结果的新证据,包括基于AR靶向治疗的单药治疗和联合策略。通过全面综述,我们希望能为TNBC找到新的治疗思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebed/12405098/907072c61e8e/12672_2025_3431_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebed/12405098/759a8059ddca/12672_2025_3431_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebed/12405098/71aea2416357/12672_2025_3431_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebed/12405098/cc4686736a18/12672_2025_3431_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebed/12405098/907072c61e8e/12672_2025_3431_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebed/12405098/759a8059ddca/12672_2025_3431_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebed/12405098/71aea2416357/12672_2025_3431_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebed/12405098/cc4686736a18/12672_2025_3431_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebed/12405098/907072c61e8e/12672_2025_3431_Fig4_HTML.jpg

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本文引用的文献

[1]
HECTD3 E3 ligase mediates ubiquitination of AKT-phosphorylated CMTM3 in HER2-overexpressed breast cancer cells.

Carcinogenesis. 2025-8-21

[2]
The Therapeutic Potential of for Psoriasis: A Combined Phytochemical, In Silico, and Experimental Approach.

Int J Mol Sci. 2025-7-28

[3]
APOBEC-Driven Hypermutation in the Lymphocyte-Predominant Group of Triple-Negative Breast Cancer.

Lab Invest. 2025-4-6

[4]
Androgen receptor-induced lncRNA SOX2-OT promotes triple-negative breast cancer tumorigenesis via targeting miR-320a-5p-CCR5 axis.

J Biol Chem. 2025-4

[5]
Divide and Conquer-Targeted Therapy for Triple-Negative Breast Cancer.

Int J Mol Sci. 2025-2-7

[6]
Immune checkpoint protein PD-L1 promotes transcription of angiogenic and oncogenic proteins IL-8, Bcl3, and STAT1 in ovarian cancer cells.

J Biol Chem. 2025-4

[7]
Darolutamide or capecitabine in triple-negative, androgen receptor-positive, advanced breast cancer (UCBG 3-06 START): a multicentre, non-comparative, randomised, phase 2 trial.

Lancet Oncol. 2025-3

[8]
Triple-negative breast cancer molecular subtypes and potential detection targets for biological therapy indications.

Carcinogenesis. 2025-4-3

[9]
Tumour cell-induced platelet aggregation in breast cancer: Scope of metal nanoparticles.

Biochim Biophys Acta Rev Cancer. 2025-4

[10]
Dual Functions of Androgen Receptor Overexpression in Triple-Negative Breast Cancer: A Complex Prognostic Marker.

Bioengineering (Basel). 2025-1-10

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