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在小鼠中构建K-Ras驱动的肺腺癌模型:治疗靶点的临床前验证

Modeling K-Ras-driven lung adenocarcinoma in mice: preclinical validation of therapeutic targets.

作者信息

Drosten Matthias, Barbacid Mariano

机构信息

Molecular Oncology Programme, Centro Nacional de Investigaciones Oncológicas (CNIO), Melchor Fernández Almagro 3, 28029, Madrid, Spain.

出版信息

J Mol Med (Berl). 2016 Feb;94(2):121-35. doi: 10.1007/s00109-015-1360-5. Epub 2015 Nov 3.

DOI:10.1007/s00109-015-1360-5
PMID:26526121
Abstract

Lung cancer is the leading cause of cancer-related deaths worldwide, and even today, the 5-year survival rate is still below 15%. Lung adenocarcinoma is the most frequent subtype, and approximately 25% of the cases harbor activating mutations in the KRAS gene. To date, there is no effective treatment for patients carrying KRAS mutations due, at least in part, to the challenge posed by direct targeting of the KRAS oncoprotein. During the last decade, scientists have developed genetically engineered mouse models that faithfully recapitulate the natural history of the human tumors. These models have been used as a preclinical platform to validate a number of relevant downstream effectors of KRAS signaling. Targets displaying synthetic lethality with the KRAS oncoprotein have also been validated in these models. Here, we review these studies and discuss their potential value in the clinical setting. We also provide an outlook as of how to improve the significance of target validation studies in preclinical platforms.

摘要

肺癌是全球癌症相关死亡的主要原因,即便在今天,其5年生存率仍低于15%。肺腺癌是最常见的亚型,约25%的病例在KRAS基因中存在激活突变。迄今为止,对于携带KRAS突变的患者尚无有效治疗方法,至少部分原因是直接靶向KRAS癌蛋白带来的挑战。在过去十年中,科学家们开发了基因工程小鼠模型,这些模型能如实地再现人类肿瘤的自然病程。这些模型已被用作临床前平台,以验证KRAS信号传导的许多相关下游效应器。与KRAS癌蛋白表现出合成致死性的靶点也在这些模型中得到了验证。在此,我们综述这些研究,并讨论它们在临床环境中的潜在价值。我们还展望了如何提高临床前平台中靶点验证研究的重要性。

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