Zhao Meng, Ramaswamy Bhuvaneswari
Meng Zhao, Bhuvaneswari Ramaswamy, Division of Medical Oncology, The Ohio State University Comprehensive Cancer Center, The Ohio State University's Wexner Medical Center, Columbus, OH 43210, United States.
World J Clin Oncol. 2014 Aug 10;5(3):248-62. doi: 10.5306/wjco.v5.i3.248.
The estrogen receptor (ER) pathway plays a critical role in breast cancer development and progression. Endocrine therapy targeting estrogen action is the most important systemic therapy for ER positive breast cancer. However its efficacy is limited by intrinsic and acquired resistance. Mechanisms responsible for endocrine resistance include deregulation of the ER pathway itself, including loss of ER expression, post-translational modification of ER, deregulation of ER co-activators; increased receptor tyrosine kinase signaling leading to activation of various intracellular pathways involved in signal transduction, proliferation and cell survival, including growth factor receptor tyrosine kinases human epidermal growth factor receptor-2, epidermal growth factor receptor, PI3K/AKT/mammalian target of rapamycin (mTOR), Mitogen activated kinase (MAPK)/ERK, fibroblast growth factor receptor, insulin-like growth factor-1 receptor; alterations in cell cycle and apoptotic machinery; Epigenetic modification including dysregulation of DNA methylation, histone modification, and nucleosome remodeling; and altered expression of specific microRNAs. Functional genomics has helped us identify a catalog of genetic and epigenetic alterations that may be exploited as potential therapeutic targets and biomarkers of response. New treatment combinations targeting ER and such oncogenic signaling pathways which block the crosstalk between these pathways have been proven effective in preclinical models. Results of recent clinical studies suggest that subsets of patients benefit from the combination of inhibitor targeting certain oncogenic signaling pathway with endocrine therapy. Especially, inhibition of the mTOR signaling pathway, a key component implicated in mediating multiple signaling cascades, offers a promising approach to restore sensitivity to endocrine therapy in breast cancer. We systematically reviewed important publications cited in PubMed, recent abstracts from ASCO annual meetings and San Antonio Breast Cancer Symposium, and relevant trials registered at ClinicalTrials.gov. We present the molecular mechanisms contributing to endocrine resistance, in particular focusing on the biological rationale for the clinical development of novel targeted agents in endocrine resistant breast cancer. We summarize clinical trials utilizing novel strategies to overcome therapeutic resistance, highlighting the need to better identify the appropriate patients whose diseases are most likely to benefit from these specific strategies.
雌激素受体(ER)通路在乳腺癌的发生和发展中起着关键作用。针对雌激素作用的内分泌治疗是ER阳性乳腺癌最重要的全身治疗方法。然而,其疗效受到内在和获得性耐药的限制。导致内分泌耐药的机制包括ER通路本身的失调,如ER表达缺失、ER的翻译后修饰、ER共激活因子的失调;受体酪氨酸激酶信号增加,导致参与信号转导、增殖和细胞存活的各种细胞内通路激活,包括生长因子受体酪氨酸激酶人表皮生长因子受体-2、表皮生长因子受体、PI3K/AKT/雷帕霉素哺乳动物靶点(mTOR)、丝裂原活化激酶(MAPK)/ERK、成纤维细胞生长因子受体、胰岛素样生长因子-1受体;细胞周期和凋亡机制的改变;表观遗传修饰,包括DNA甲基化失调、组蛋白修饰和核小体重塑;以及特定微小RNA的表达改变。功能基因组学帮助我们识别了一系列遗传和表观遗传改变,这些改变可被用作潜在的治疗靶点和反应生物标志物。针对ER和此类致癌信号通路的新治疗组合,阻断这些通路之间的相互作用,已在临床前模型中被证明有效。近期临床研究结果表明,部分患者受益于靶向某些致癌信号通路的抑制剂与内分泌治疗的联合应用。特别是,抑制mTOR信号通路,这一参与介导多种信号级联反应的关键成分,为恢复乳腺癌对内分泌治疗的敏感性提供了一种有前景的方法。我们系统回顾了PubMed中引用的重要出版物、美国临床肿瘤学会年会和圣安东尼奥乳腺癌研讨会的近期摘要,以及在ClinicalTrials.gov注册的相关试验。我们阐述了导致内分泌耐药的分子机制,尤其关注内分泌耐药乳腺癌中新型靶向药物临床开发的生物学原理。我们总结了利用新策略克服治疗耐药的临床试验,强调需要更好地识别那些最有可能从这些特定策略中获益的合适患者。