结直肠癌
微卫星不稳定性
肿瘤微环境
免疫系统
癌症
微生物群
免疫检查点
医学
肿瘤科
封锁
免疫疗法
生物
免疫学
生物信息学
内科学
基因
受体
等位基因
微卫星
生物化学
作者
Ce Yuan,Xianda Zhao,Dechen Wangmo,Duha Alshareef,Travis J. Gates,Subbaya Subramanian
标识
DOI:10.1016/j.pharmthera.2021.107981
摘要
Despite significant advances over the past 2 decades in preventive screening and therapy aimed at improving patient survival, colorectal cancer (CRC) remains the second most common cause of cancer death in the United States. The average 5-year survival rate of CRC patients with positive regional lymph nodes is only 40%, while less than 5% of patients with distant metastases survive beyond 5 years. There is a critical need to develop novel therapies that can improve overall survival in patients with poor prognoses, particularly since 60% of them are diagnosed at an advanced stage. Pertinently, immune checkpoint blockade therapy has dramatically changed how we treat CRC patients with microsatellite-instable high tumors. Furthermore, accumulating evidence shows that changes in gut microbiota are associated with the regulation of host antitumor immune response and cancer progression. Appropriate animal models are essential to deciphering the complex mechanisms of host antitumor immune response and tumor-gut microbiome metabolic interactions. Here, we discuss various mouse models of colorectal cancer that are developed to address key questions on tumor immune response and tumor-microbiota interactions. These CRC models will also serve as resourceful tools for effective preclinical studies.
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