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鳞状细胞肺癌的小鼠模型:对药物发现的影响。

Mouse models in squamous cell lung cancer: impact for drug discovery.

机构信息

a Department of Oncology , Montefiore Medical Center/Albert Einstein College of Medicine , Bronx , NY , USA.

b Department of Medicine , Montefiore Medical Center/Albert Einstein College of Medicine , Bronx , NY , USA.

出版信息

Expert Opin Drug Discov. 2018 Apr;13(4):347-358. doi: 10.1080/17460441.2018.1437137. Epub 2018 Feb 15.

Abstract

Squamous cell lung cancer (SQCLC) is the second most common subtype of non-small cell lung cancer (NSCLC) and has limited therapeutic options. Its development is likely a result of a multistep process in response to chronic tobacco exposure, involving sequential metaplasia, dysplasia and invasive carcinoma. Its complex genomic landscape has recently been revealed but no driver mutations have been validated that could lead to molecularly targeted therapy as have emerged in lung adenocarcinoma. Few preclinical murine models exist for testing and developing novel therapeutics in SQCLC. Areas covered: This review discusses the pathophysiology and molecular underpinnings of SQCLC that have limited the development of animal models. It then explores the advantages and limitations of a variety of existing mouse models and illustrates their potential application in drug discovery and chemoprevention. Expert opinion: There are several challenges in the development of mouse models for SQCLC, such as lack of validated driver genetic alterations, unclear cell of origin, and difficulty in reproducing the sophisticated tumor microenvironment of human disease. Nevertheless, several successful SQCLC murine models have emerged, especially Patient Derived Xenografts (PDXs) and Genetically Engineered Mouse Models (GEMMs). Continued efforts are needed to generate more SQCLC animal models to better understand its carcinogenesis and metastasis and to further test novel therapeutic strategies.

摘要

鳞状细胞肺癌(SQCLC)是第二常见的非小细胞肺癌(NSCLC)亚型,治疗选择有限。它的发展可能是对慢性烟草暴露的多步反应的结果,涉及连续的化生、发育不良和浸润性癌。其复杂的基因组景观最近已经被揭示出来,但没有像在肺腺癌中那样出现的驱动突变,可以导致分子靶向治疗。用于测试和开发 SQCLC 新型疗法的临床前小鼠模型很少。

涵盖领域

本文讨论了 SQCLC 的病理生理学和分子基础,这些基础限制了动物模型的发展。然后探讨了各种现有小鼠模型的优缺点,并说明了它们在药物发现和化学预防中的潜在应用。

专家意见

SQCLC 小鼠模型的开发存在几个挑战,例如缺乏经过验证的驱动基因突变、不清楚的起始细胞以及难以复制人类疾病复杂的肿瘤微环境。然而,已经出现了几种成功的 SQCLC 小鼠模型,特别是患者来源的异种移植物(PDX)和基因工程小鼠模型(GEMM)。需要继续努力生成更多的 SQCLC 动物模型,以更好地理解其致癌和转移,并进一步测试新型治疗策略。

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