Chen Yongkang, Yang Yong, Gu Jin
Department of Gastrointestinal Surgery III, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Peking University Cancer Hospital & Institute, Beijing 100142, People's Republic of China.
Department of Gastrointestinal Surgery, Peking University Shougang Hospital, Beijing 100144, People's Republic of China.
Cancer Manag Res. 2020 Jun 9;12:4117-4128. doi: 10.2147/CMAR.S240108. eCollection 2020.
Intestinal microbiome influences host immunity and several diseases, including cancer, in their areas of colonization. Microbial dysbiosis and over-colonization of specific microbes within the colorectal mucosa can impact the progress of carcinogenesis. Investigations initially focused on the mechanisms by which the intestinal microbiome initiates or promotes the development of colorectal cancer, including DNA damage, induction of chromosomal instability, and regulation of host immune responses. Some studies on the clinicopathological features have reported that specific strains present at high abundance are associated with advanced stage and positive lymph nodes in colorectal cancer. In this context, we reviewed the relationship between the intestinal microbiome and the clinical features (patient age, disease staging, prognosis, etc.) of patients with colorectal cancer, and evaluated the potential pathogenesis caused by the intestinal microbiome in disease progress. This article assessed whether changes in distinct species or strains occur during the period of cancer advancement. Overall, age grouping does not bring about significant differences in the constitution of microbiome. The disease stages show their distinct distribution in some species and strains. Oncogenic species are generally enriched in patients with poor prognosis, including low infiltration of CD3 T cells, poor differentiation, widespread invasion, high microsatellite instability, CpG island methylator phenotype, BRAF mutation, short overall survival, and disease-free survival. The implications of those changes we discussed may assist in comprehensive understanding of the tumorigenesis of colorectal cancer from a microbiological perspective, finding potential biomarkers for colorectal cancer.
肠道微生物群在其定植区域影响宿主免疫和包括癌症在内的多种疾病。微生物群落失调以及结直肠黏膜内特定微生物的过度定植会影响致癌作用的进程。最初的研究集中在肠道微生物群启动或促进结直肠癌发展的机制上,包括DNA损伤、诱导染色体不稳定以及调节宿主免疫反应。一些关于临床病理特征的研究报告称,高丰度存在的特定菌株与结直肠癌的晚期和阳性淋巴结相关。在此背景下,我们回顾了肠道微生物群与结直肠癌患者临床特征(患者年龄、疾病分期、预后等)之间的关系,并评估了肠道微生物群在疾病进展中引起的潜在发病机制。本文评估了在癌症进展期间不同物种或菌株是否发生变化。总体而言,年龄分组在微生物群组成上不会带来显著差异。疾病分期在某些物种和菌株中显示出其独特的分布。致癌物种通常在预后不良的患者中富集,包括CD3 T细胞低浸润、低分化、广泛侵袭、高微卫星不稳定性、CpG岛甲基化表型、BRAF突变、总生存期短和无病生存期短。我们讨论的这些变化的意义可能有助于从微生物学角度全面理解结直肠癌的肿瘤发生,寻找结直肠癌的潜在生物标志物。