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合成致死性:开发更明智癌症疗法的框架。

Synthetic lethality: a framework for the development of wiser cancer therapeutics.

机构信息

Howard Hughes Medical Institute, Dana-Farber Cancer Institute and Brigham and Women's Hospital, 44 Binney St, Boston, MA 02115, USA.

出版信息

Genome Med. 2009 Oct 27;1(10):99. doi: 10.1186/gm99.

Abstract

The challenge in medical oncology has always been to identify compounds that will kill, or at least tame, cancer cells while leaving normal cells unscathed. Most chemotherapeutic agents in use today were selected primarily for their ability to kill rapidly dividing cancer cells grown in cell culture and in mice, with their selectivity determined empirically during subsequent animal and human testing. Unfortunately, most of the drugs developed in this way have relatively low therapeutic indices (low toxic dose relative to the therapeutic dose). Recent advances in genomics are leading to a more complete picture of the range of mutations, both driver and passenger, present in human cancers. Synthetic lethality provides a conceptual framework for using this information to arrive at drugs that will preferentially kill cancer cells relative to normal cells. It also provides a possible way to tackle 'undruggable' targets. Two genes are synthetically lethal if mutation of either gene alone is compatible with viability but simultaneous mutation of both genes leads to death. If one is a cancer-relevant gene, the task is to discover its synthetic lethal interactors, because targeting these would theoretically kill cancer cells mutant in the cancer-relevant gene while sparing cells with a normal copy of that gene. All cancer drugs in use today, including conventional cytotoxic agents and newer 'targeted' agents, target molecules that are present in both normal cells and cancer cells. Their therapeutic indices almost certainly relate to synthetic lethal interactions, even if those interactions are often poorly understood. Recent technical advances enable unbiased screens for synthetic lethal interactors to be undertaken in human cancer cells. These approaches will hopefully facilitate the discovery of safer, more efficacious anticancer drugs that exploit vulnerabilities that are unique to cancer cells by virtue of the mutations they have accrued during tumor progression.

摘要

医学肿瘤学的挑战一直是确定能够杀死或至少驯服癌细胞而不损伤正常细胞的化合物。目前使用的大多数化疗药物主要是根据它们在细胞培养和小鼠中快速分裂的癌细胞的杀伤能力选择的,其选择性在随后的动物和人体试验中通过经验确定。不幸的是,以这种方式开发的大多数药物的治疗指数相对较低(相对于治疗剂量的毒性剂量较低)。基因组学的最新进展使人们对人类癌症中存在的驱动突变和乘客突变的范围有了更全面的了解。合成致死性为利用这些信息开发出相对于正常细胞更优先杀死癌细胞的药物提供了一个概念框架。它还为解决“不可成药”靶点提供了一种可能的方法。如果单独突变任一个基因是相容的,但同时突变两个基因会导致死亡,则两个基因是合成致死的。如果其中一个是癌症相关基因,则任务是发现其合成致死相互作用体,因为靶向这些基因理论上会杀死在癌症相关基因中发生突变的癌细胞,而不会杀死具有该基因正常副本的细胞。目前使用的所有癌症药物,包括传统的细胞毒性药物和较新的“靶向”药物,都针对存在于正常细胞和癌细胞中的分子。它们的治疗指数几乎肯定与合成致死相互作用有关,即使这些相互作用往往理解得很差。最近的技术进步使得可以在人类癌细胞中进行合成致死相互作用的无偏筛选。这些方法有望促进发现更安全、更有效的抗癌药物,这些药物利用由于肿瘤进展而积累的突变而使癌细胞独有的脆弱性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30e1/2784312/45d1c338a616/gm99-1.jpg

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