Kucherlapati Melanie Haas
Department of Genetics, Harvard Medical School, Boston, MA, USA.
Department of Medicine, Division of Genetics, Brigham and Women's Hospital, Boston, MA, USA.
iScience. 2023 May 25;26(6):106958. doi: 10.1016/j.isci.2023.106958. eCollection 2023 Jun 16.
Mouse models of colorectal cancer (CRC) have been crucial in the identification of the role of genes responsible for the full range of pathology of the human disease and have proved to be dependable for testing anti-cancer drugs. Recent research points toward the relevance of tumor, angiogenic, and immune microenvironments in CRC progression to late-stage disease, as well as the treatment of it. This study examines important mouse models in CRC, discussing inherent strengths and weaknesses disclosed during their construction. It endeavors to provide both a synopsis of previous work covering how investigators have defined various models and to evaluate critically how researchers are most likely to use them in the future. Accumulated evidence regarding the metastatic process and the hope of using checkpoint inhibitors and immunological inhibitor therapies points to the need for a genetically engineered mouse model that is both immunocompetent and autochthonous.
结直肠癌(CRC)小鼠模型对于确定导致人类疾病全部病理过程的基因作用至关重要,并且已被证明在抗癌药物测试中是可靠的。最近的研究表明,肿瘤、血管生成和免疫微环境在CRC进展至晚期疾病以及其治疗中具有相关性。本研究考察了CRC中的重要小鼠模型,讨论了在构建过程中所揭示的固有优缺点。它致力于既概述先前关于研究人员如何定义各种模型的工作,又批判性地评估研究人员未来最有可能如何使用它们。关于转移过程的累积证据以及使用检查点抑制剂和免疫抑制剂疗法的希望表明,需要一种具有免疫活性且源自自身的基因工程小鼠模型。