Incheol Seo, S. Bae, Shin Kim, W. Jeong, S. Baek
{"title":"Analysis of Intestinal Mucosal Microbiome Changes before and after Chemoradiation in Locally Advanced Rectal Cancer Patients","authors":"Incheol Seo, S. Bae, Shin Kim, W. Jeong, S. Baek","doi":"10.4167/jbv.2019.49.4.162","DOIUrl":null,"url":null,"abstract":"©This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/ license/by-nc/3.0/). Purpose: Dysbiosis of gut microbiota has been reported to participate in the pathogenesis of colorectal cancer, but changes in microbiota due to radiotherapy have not been studied. In this study, we tried to elucidate the changes in the microbiome in rectal cancer after chemoradiotherapy using RNA sequencing analysis. Materials and methods: We included 11 pairs of human rectal cancer tissues before and after irradiation between August 2016 and December 2017 and performed RNA sequencing analysis. Mapped reads to human reference genomes were used for pair-wise transcriptome comparisons, and unmapped (non-human) reads were then mapped to bacterial marker genes using PathSeq. Results: At microbiome level, interindividual variability of mucosal microbiota was greater than the change in microbial composition during radiotherapy. This indicates that rapid homeostatic recovery of the mucosal microbial composition takes place short after radiotherapy. At single microbe level, Prevotella and Fusobacterium, which were identified as important causative microbes of the initiation and progression of rectal cancer were decreased by radiotherapy. Moreover, changes in Prevotella were associated with changes in the human transcriptome of rectal cancer. We also found that there was a gene cluster that increased and decreased in association with changes in microbial composition by chemoradiation. Conclusion: This study revealed changes in tumor-associated microbial community by irradiation in rectal cancer. These findings can be used to develop a new treatment strategy of neoadjuvant therapy for locally advanced rectal cancer by overcoming radio-resistance or facilitating radio-sensitivity.","PeriodicalId":39739,"journal":{"name":"Journal of Bacteriology and Virology","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2019-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Bacteriology and Virology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4167/jbv.2019.49.4.162","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Immunology and Microbiology","Score":null,"Total":0}
引用次数: 0
局部晚期直肠癌患者放化疗前后肠黏膜微生物组变化分析
©这是一篇基于知识共享署名非商业许可协议(http://creativecommons.org/ License /by-nc/3.0/)的开放获取文章。目的:有报道称肠道菌群失调参与了结直肠癌的发病,但尚未对放疗引起的肠道菌群变化进行研究。在这项研究中,我们试图通过RNA测序分析来阐明直肠癌放化疗后微生物组的变化。材料与方法:选取2016年8月至2017年12月辐照前后的11对人直肠癌组织,进行RNA测序分析。绘制的人类参考基因组序列用于成对转录组比较,然后使用PathSeq将未绘制的(非人类)序列映射到细菌标记基因。结果:在微生物组水平上,放疗期间粘膜微生物群的个体间变异性大于微生物组成的变化。这表明,粘膜微生物组成的快速稳态恢复发生在放疗后不久。在单个微生物水平上,普雷沃菌和梭杆菌被认为是直肠癌发生和发展的重要致病微生物,放射治疗减少了它们的数量。此外,普雷沃氏菌的变化与人类直肠癌转录组的变化有关。我们还发现,有一个基因簇的增加和减少与放化疗微生物组成的变化有关。结论:本研究揭示了辐照对直肠癌肿瘤相关微生物群落的影响。这些发现可用于通过克服放射耐药或促进放射敏感性来开发局部晚期直肠癌新辅助治疗的新策略。
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