三阴乳腺癌的分子分型及靶向、免疫和中药治疗研究进展
Research Progress on Molecular Subtyping, Targeted Therapy, Immunotherapy, and Traditional Chinese Medicine-Based Interventions for Triple-Negative Breast Cancer
DOI: 10.12677/wjcr.2026.162013, PDF,   
作者: 张仕玉*, 刘 泉, 刘嘉敏, 李 霁#:昆明医科大学药学院暨云南省天然药物药理重点实验室,云南 昆明;云南省现代生物医药产业学院,云南 昆明;刘 勤#:云南省食品药品监督检验研究院,云南 昆明
关键词: 三阴乳腺癌分子分型信号通路靶向治疗免疫治疗中药联合其他药物Triple-Negative Breast Cancer Molecular Subtyping Signaling Pathways Targeted Therapy Immunotherapy Traditional Chinese Medicine Combined with Other Drugs
摘要: 三阴性乳腺癌(TNBC)是乳腺癌的一种高度侵袭性亚型,负表达雌激素受体(ER)、孕激素受体(PR)和人表皮生长因子受体2 (HER2)。化疗是TNBC患者的主要全身性治疗手段,但其疗效不尽如人意,且常伴随显著的治疗相关毒副作用。当务之急是寻找更有效的疗法。根据TNBC中表达的特定分子和信号通路,已经出现了多种靶向治疗策略,包括PI3K/AKT/mTOR抑制剂、表皮生长因子受体抑制剂、Notch抑制剂、聚ADP-核糖聚合酶抑制剂和AR抑制剂。本文系统梳理了三阴性乳腺癌(TNBC)的分子分型,免疫治疗、靶向治疗和中药联合其他药物等多种治疗策略,旨在为TNBC个体化治疗的未来发展提供参考与方向。
Abstract: Triple-negative breast cancer (TNBC) is a highly aggressive subtype of breast cancer characterized by the lack of expression of estrogen receptor (ER), progesterone receptor (PR), and human epidermal growth factor receptor 2 (HER2). Chemotherapy remains the primary systemic treatment for TNBC patients; however, its efficacy is often suboptimal and accompanied by significant treatment-related toxicities. There is a pressing need to develop more effective therapeutic approaches. In recent years, various targeted therapeutic strategies have emerged based on specific molecules and signaling pathways implicated in TNBC, including inhibitors of PI3K/AKT/mTOR, epidermal growth factor receptor, Notch, poly ADP-ribose polymerase (PARP), and androgen receptor (AR). This article systematically reviews the molecular subtypes of triple-negative breast cancer (TNBC), as well as various treatment strategies for TNBC, including immunotherapy, targeted therapy, and the combination of traditional Chinese medicine with other drugs, which aims to offer insights and direction for the future development of personalized therapy for TNBC.
文章引用:张仕玉, 刘泉, 刘嘉敏, 刘勤, 李霁. 三阴乳腺癌的分子分型及靶向、免疫和中药治疗研究进展[J]. 世界肿瘤研究, 2026, 16(2): 113-125. https://doi.org/10.12677/wjcr.2026.162013

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