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肿瘤学研究与癌症医学中的基因工程小鼠模型

Genetically engineered mouse models in oncology research and cancer medicine.

作者信息

Kersten Kelly, de Visser Karin E, van Miltenburg Martine H, Jonkers Jos

机构信息

Division of Immunology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.

Division of Molecular Pathology and Cancer Genomics Netherlands, The Netherlands Cancer Institute, Amsterdam, The Netherlands

出版信息

EMBO Mol Med. 2017 Feb;9(2):137-153. doi: 10.15252/emmm.201606857.

Abstract

Genetically engineered mouse models (GEMMs) have contributed significantly to the field of cancer research. In contrast to cancer cell inoculation models, GEMMs develop de novo tumors in a natural immune-proficient microenvironment. Tumors arising in advanced GEMMs closely mimic the histopathological and molecular features of their human counterparts, display genetic heterogeneity, and are able to spontaneously progress toward metastatic disease. As such, GEMMs are generally superior to cancer cell inoculation models, which show no or limited heterogeneity and are often metastatic from the start. Given that GEMMs capture both tumor cell-intrinsic and cell-extrinsic factors that drive de novo tumor initiation and progression toward metastatic disease, these models are indispensable for preclinical research. GEMMs have successfully been used to validate candidate cancer genes and drug targets, assess therapy efficacy, dissect the impact of the tumor microenvironment, and evaluate mechanisms of drug resistance. In vivo validation of candidate cancer genes and therapeutic targets is further accelerated by recent advances in genetic engineering that enable fast-track generation and fine-tuning of GEMMs to more closely resemble human patients. In addition, aligning preclinical tumor intervention studies in advanced GEMMs with clinical studies in patients is expected to accelerate the development of novel therapeutic strategies and their translation into the clinic.

摘要

基因工程小鼠模型(GEMMs)对癌症研究领域做出了重大贡献。与癌细胞接种模型不同,GEMMs在天然免疫健全的微环境中产生原发性肿瘤。晚期GEMMs中出现的肿瘤与人类对应肿瘤的组织病理学和分子特征极为相似,表现出基因异质性,并且能够自发进展为转移性疾病。因此,GEMMs通常优于癌细胞接种模型,后者表现出无或有限的异质性,且往往从一开始就具有转移性。鉴于GEMMs捕捉了驱动原发性肿瘤起始和向转移性疾病进展的肿瘤细胞内在和细胞外在因素,这些模型对于临床前研究不可或缺。GEMMs已成功用于验证候选癌症基因和药物靶点、评估治疗效果、剖析肿瘤微环境的影响以及评估耐药机制。基因工程的最新进展进一步加速了候选癌症基因和治疗靶点的体内验证,这些进展使GEMMs能够快速生成并进行微调,以更接近人类患者。此外,将晚期GEMMs中的临床前肿瘤干预研究与患者的临床研究相结合,有望加速新型治疗策略的开发及其向临床的转化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d1c/5286388/f852a304a33a/EMMM-9-137-g001.jpg

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