Sabaawy Hatem E
Department of Medicine, Rutgers-Robert Wood Johnson Medical School, USA ; Department of Cellular and Molecular Pharmacology, Rutgers-Robert Wood Johnson Medical School, USA ; Rutgers Cancer Institute of New Jersey, New Brunswick, NJ 08903-2681, USA.
J Leuk (Los Angel). 2013 Nov 18;1(4):1000124. doi: 10.4172/2329-6917.1000124.
The efficacy of targeted therapies in leukemias and solid tumors depends upon the accurate detection and sustained targeting of initial and evolving driver mutations and/or aberrations in cancer cells. Tumor clonal evolution of the diverse populations of cancer cells during cancer progression contributes to the longitudinal variations of clonal, morphological, anatomical, and molecular heterogeneity of tumors. Moreover, drug-resistant subclones present at initiation of therapy or emerging as a result of targeted therapies represent major challenges for achieving success of personalized therapies in providing meaningful improvement in cancer survival rates. Here, I briefly portray tumor cell clonal evolution at the cellular and molecular levels, and present the multiple types of genetic heterogeneity in tumors, with a focus on their impact on the implementation of personalized or precision cancer medicine.
靶向疗法在白血病和实体瘤中的疗效取决于对癌细胞中初始和演变的驱动突变及/或畸变的准确检测和持续靶向。癌症进展过程中癌细胞不同群体的肿瘤克隆进化导致肿瘤的克隆、形态、解剖和分子异质性的纵向变化。此外,治疗开始时就存在或因靶向治疗而出现的耐药亚克隆是实现个性化治疗成功提高癌症生存率的主要挑战。在此,我简要描述细胞和分子水平上的肿瘤细胞克隆进化,并介绍肿瘤中多种类型的基因异质性,重点是它们对个性化或精准癌症医学实施的影响。