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通过改进生物标志物整合克服多基因癌症耐药性的肿瘤内异质性。

Overcoming intratumor heterogeneity of polygenic cancer drug resistance with improved biomarker integration.

机构信息

Department of Radiation Oncology, University of Michigan School of Medicine, Ann Arbor, MI 48109-2200, USA.

出版信息

Neoplasia. 2012 Dec;14(12):1278-89. doi: 10.1593/neo.122096.

Abstract

Improvements in technology and resources are helping to advance our understanding of cancer-initiating events as well as factors involved with tumor progression, adaptation, and evasion of therapy. Tumors are well known to contain diverse cell populations and intratumor heterogeneity affords neoplasms with a diverse set of biologic characteristics that can be used to evolve and adapt. Intratumor heterogeneity has emerged as a major hindrance to improving cancer patient care. Polygenic cancer drug resistance necessitates reconsidering drug designs to include polypharmacology in pursuit of novel combinatorial agents having multitarget activity to overcome the diverse and compensatory signaling pathways in which cancer cells use to survive and evade therapy. Advances will require integration of different biomarkers such as genomics and imaging to provide for more adequate elucidation of the spatially varying location, type, and extent of diverse intratumor signaling molecules to provide for a rationale-based personalized cancer medicine strategy.

摘要

技术和资源的进步有助于增进我们对癌症起始事件以及肿瘤进展、适应和逃避治疗相关因素的理解。众所周知,肿瘤内含有多种细胞群体,肿瘤内异质性使肿瘤具有一系列不同的生物学特征,这些特征可用于进化和适应。肿瘤内异质性已成为改善癌症患者治疗的主要障碍。多基因癌症药物耐药性需要重新考虑药物设计,将多药理学纳入其中,以寻求具有多靶点活性的新型组合药物,从而克服癌细胞用于存活和逃避治疗的多样化和补偿性信号通路。这些进展需要整合不同的生物标志物,如基因组学和影像学,以更充分地阐明肿瘤内不同信号分子的空间变化位置、类型和程度,从而为基于合理的个体化癌症治疗策略提供依据。

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