Turashvili Gulisa, Brogi Edi
Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, United States.
Front Med (Lausanne). 2017 Dec 8;4:227. doi: 10.3389/fmed.2017.00227. eCollection 2017.
Breast cancer is a heterogeneous disease and differs greatly among different patients (intertumor heterogeneity) and even within each individual tumor (intratumor heterogeneity). Clinical and morphologic intertumor heterogeneity is reflected by staging systems and histopathologic classification of breast cancer. Heterogeneity in the expression of established prognostic and predictive biomarkers, hormone receptors, and human epidermal growth factor receptor 2 oncoprotein is the basis for targeted treatment. Molecular classifications are indicators of genetic tumor heterogeneity, which is probed with multigene assays and can lead to improved stratification into low- and high-risk groups for personalized therapy. Intratumor heterogeneity occurs at the morphologic, genomic, transcriptomic, and proteomic levels, creating diagnostic and therapeutic challenges. Understanding the molecular and cellular mechanisms of tumor heterogeneity that are relevant to the development of treatment resistance is a major area of research. Despite the improved knowledge of the complex genetic and phenotypic features underpinning tumor heterogeneity, there has been only limited advancement in diagnostic, prognostic, or predictive strategies for breast cancer. The current guidelines for reporting of biomarkers aim to maximize patient eligibility for targeted therapy, but do not take into account intratumor heterogeneity. The molecular classification of breast cancer is not implemented in routine clinical practice. Additional studies and in-depth analysis are required to understand the clinical significance of rapidly accumulating data. This review highlights inter- and intratumor heterogeneity of breast carcinoma with special emphasis on pathologic findings, and provides insights into the clinical significance of molecular and cellular mechanisms of heterogeneity.
乳腺癌是一种异质性疾病,在不同患者之间(肿瘤间异质性)甚至在每个肿瘤内部(肿瘤内异质性)都存在很大差异。乳腺癌的分期系统和组织病理学分类反映了临床和形态学上的肿瘤间异质性。既定预后和预测生物标志物、激素受体以及人表皮生长因子受体2癌蛋白表达的异质性是靶向治疗的基础。分子分类是肿瘤基因异质性的指标,可通过多基因检测进行探究,并有助于改善分层,将患者分为低风险和高风险组以进行个性化治疗。肿瘤内异质性发生在形态学、基因组、转录组和蛋白质组水平,带来了诊断和治疗方面的挑战。了解与治疗耐药性发展相关的肿瘤异质性的分子和细胞机制是一个主要的研究领域。尽管对支撑肿瘤异质性的复杂遗传和表型特征有了更多了解,但乳腺癌的诊断、预后或预测策略进展有限。目前的生物标志物报告指南旨在使患者最大限度地符合靶向治疗条件,但未考虑肿瘤内异质性。乳腺癌的分子分类在常规临床实践中并未实施。需要进行更多研究和深入分析,以了解快速积累的数据的临床意义。本综述重点介绍了乳腺癌的肿瘤间和肿瘤内异质性,特别强调了病理结果,并深入探讨了异质性分子和细胞机制的临床意义。