遗传异质性
肿瘤异质性
生物
癌症
乳腺癌
癌症的体细胞进化
表观遗传学
表型
大规模并行测序
外科肿瘤学
癌症干细胞
单细胞测序
肿瘤异质性
计算生物学
进化生物学
遗传学
医学
肿瘤科
基因组
基因
外显子组测序
作者
Luciano G. Martelotto,Charlotte K.Y. Ng,Salvatore Piscuoglio,Britta Weigelt,Jorge S. Reis‐Filho
摘要
In recent years it has become clear that cancer cells within a single tumor can display striking morphological, genetic and behavioral variability. Burgeoning genetic, epigenetic and phenomenological data support the existence of intra-tumor genetic heterogeneity in breast cancers; however, its basis is yet to be fully defined. Two of the most widely evoked concepts to explain the origin of heterogeneity within tumors are the cancer stem cell hypothesis and the clonal evolution model. Although the cancer stem cell model appeared to provide an explanation for the variability among the neoplastic cells within a given cancer, advances in massively parallel sequencing have provided several lines of evidence to suggest that intra-tumor genetic heterogeneity likely plays a fundamental role in the phenotypic heterogeneity observed in cancers. Many challenges remain, however, in the interpretation of the next generation sequencing results obtained so far. Here we review the models that explain tumor heterogeneity, the causes of intra-tumor genetic diversity and their impact on our understanding and management of breast cancer, methods to study intra-tumor heterogeneity and the assessment of intra-tumor genetic heterogeneity in the clinic.
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