Tumor heterogeneity: Causes and consequences

被引:1183
作者
Marusyk, Andriy [1 ]
Polyak, Kornelia [1 ]
机构
[1] Harvard Univ, Brigham & Womens Hosp, Sch Med,Dept Med, Dana Farber Canc Inst,Dept Med Oncol, Boston, MA 02115 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER | 2010年 / 1805卷 / 01期
关键词
Diversity; Selection; Evolution; COMPARATIVE GENOMIC HYBRIDIZATION; ACUTE LYMPHOBLASTIC-LEUKEMIA; CANCER STEM-CELLS; BREAST-CANCER; CLONAL EVOLUTION; GENETIC-HETEROGENEITY; KARYOTYPIC COMPARISONS; MYELOID-LEUKEMIA; FLOW-CYTOMETRY; RECEPTOR GENE;
D O I
10.1016/j.bbcan.2009.11.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
With rare exceptions, spontaneous tumors originate from a single cell. Yet, at the time of clinical diagnosis, the majority of human tumors display startling heterogeneity in many morphological and physiological features, such as expression of cell surface receptors, proliferative and angiogenic potential. To a substantial extent, this heterogeneity might be attributed to morphological and epigenetic plasticity, but there is also strong evidence for the co-existence of genetically divergent tumor cell clones within tumors. In this perspective, we summarize the sources of intra-tumor phenotypic heterogeneity with emphasis on genetic heterogeneity. We review experimental evidence for the existence of both intra-tumor clonal heterogeneity as well as frequent evolutionary divergence between primary tumors and metastatic outgrowths. Furthermore, we discuss potential biological and clinical implications of intra-tumor clonal heterogeneity. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:105 / 117
页数:13
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