Kutasovic Jamie R, McCart Reed Amy E, Sokolova Anna, Lakhani Sunil R, Simpson Peter T
UQ Centre for Clinical Research, Faculty of Medicine, The University of Queensland, Herston, Brisbane 4029, Australia.
QIMR Berghofer Medical Research Institute, Herston 4006, Australia.
Cancers (Basel). 2020 Mar 31;12(4):848. doi: 10.3390/cancers12040848.
Breast cancer is a remarkably complex and diverse disease. Subtyping based on morphology, genomics, biomarkers and/or clinical parameters seeks to stratify optimal approaches for management, but it is clear that every breast cancer is fundamentally unique. Intra-tumour heterogeneity adds further complexity and impacts a patient's response to neoadjuvant or adjuvant therapy. Here, we review some established and more recent evidence related to the complex nature of breast cancer evolution. We describe morphologic and genomic diversity as it arises spontaneously during the early stages of tumour evolution, and also in the context of treatment where the changing subclonal architecture of a tumour is driven by the inherent adaptability of tumour cells to evolve and resist the selective pressures of therapy.
乳腺癌是一种极其复杂多样的疾病。基于形态学、基因组学、生物标志物和/或临床参数进行亚型分类,旨在为治疗分层出最佳方法,但显然每例乳腺癌本质上都是独特的。肿瘤内异质性增加了进一步的复杂性,并影响患者对新辅助或辅助治疗的反应。在此,我们回顾一些与乳腺癌演变复杂性相关的已确立及最新证据。我们描述了肿瘤演变早期自发出现的形态学和基因组多样性,以及在治疗背景下肿瘤亚克隆结构的变化,这种变化是由肿瘤细胞固有的进化和抵抗治疗选择压力的适应性所驱动的。