Cancer heterogeneity: implications for targeted therapeutics

被引:690
作者
Fisher, R. [1 ,2 ]
Pusztai, L. [3 ]
Swanton, C. [1 ,4 ]
机构
[1] UCL, Inst Canc, London, England
[2] Royal Marsden Hosp, Dept Med, London SW3 6JJ, England
[3] Yale Univ, Ctr Canc, New Haven, CT USA
[4] Canc Res UK London Res Inst, Translat Canc Therapeut Lab, Lincolns Inn Fields 44, London WC2A 3LY, England
关键词
intra-tumour; heterogeneity; next-generation sequencing; therapeutics; ACUTE MYELOID-LEUKEMIA; CELL LUNG-CANCER; CHROMOSOMAL INSTABILITY; BREAST-CANCER; CLONAL EVOLUTION; TUMOR HETEROGENEITY; ACQUIRED-RESISTANCE; PANCREATIC-CANCER; MULTIPLE-MYELOMA; T790M MUTATION;
D O I
10.1038/bjc.2012.581
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Developments in genomic techniques have provided insight into the remarkable genetic complexity of malignant tumours. There is increasing evidence that solid tumours may comprise of subpopulations of cells with distinct genomic alterations within the same tumour, a phenomenon termed intra-tumour heterogeneity. Intra-tumour heterogeneity is likely to have implications for cancer therapeutics and biomarker discovery, particularly in the era of targeted treatment, and evidence for a relationship between intra-tumoural heterogeneity and clinical outcome is emerging. Our understanding of the processes that exacerbate intra-tumoural heterogeneity, both iatrogenic and tumour specific, is likely to increase with the development and more widespread implementation of advanced sequencing technologies, and adaptation of clinical trial design to include comprehensive tissue collection protocols. The current evidence for intra-tumour heterogeneity and its relevance to cancer therapeutics will be presented in this mini-review.
引用
收藏
页码:479 / 485
页数:7
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