Novel molecular targets in cancer chemotherapy waiting for discovery.

Conrad Kunick
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引用次数: 7

Abstract

Despite a number of advances in the past decades the medicinal cancer therapy is hampered by problems of severe unwanted side effects and the development of resistances. Many established anti-cancer drugs are directed toward targets that are not specific for cancer but are essential biochemical molecules in living cells. Because cancer cells do not only carry one but multiple genetic alterations which are more characteristic for the individual patient than for the tumor entity, an individualized medicinal approach could improve the success of a tumor therapy. A prerequisite for personalized tumor therapies is an upgrade of the array of anticancer drugs directed to different molecular targets. Therefore, a systematic search for anticancer drug targets should constitute a research priority. The database of fingerprints of new chemical entities generated in the National Cancer Institute's Anticancer Drug Screening is a rich source of novel targets which might be uncovered by the interdisciplinary application of methods from bioinformatics, biochemistry, chemistry, tumor biology and related sciences.

癌症化疗的新分子靶点有待发现。
尽管在过去的几十年里取得了一些进步,但药物癌症治疗受到严重副作用和耐药性发展问题的阻碍。许多已建立的抗癌药物针对的目标不是针对癌症的,而是活细胞中必不可少的生化分子。由于癌细胞不仅携带一种而是多种基因改变,这些基因改变对个体患者而言比对肿瘤实体而言更具特征,因此个体化的治疗方法可以提高肿瘤治疗的成功率。个性化肿瘤治疗的先决条件是针对不同分子靶点的抗癌药物阵列的升级。因此,系统地寻找抗癌药物靶点应成为研究重点。国家癌症研究所抗癌药物筛选项目中产生的新化学实体指纹数据库是一个丰富的新靶点来源,可以通过生物信息学、生物化学、化学、肿瘤生物学和相关科学方法的跨学科应用来发现新的靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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