Caulobacter and Novosphingobium in tumor tissues are associated with colorectal cancer outcomes

Diversity and composition of the gut microbiome are associated with cancer patient outcomes including colorectal cancer (CRC). A growing number of evidence indicates that (Fn) in CRC tissue is associated with worse survival. However, few studies have further analyzed the differences in bacteria in t...

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Published inFrontiers in oncology Vol. 12; p. 1078296
Main Authors Zhou, Bin, Shi, Linli, Jin, Min, Cheng, Mingxia, Yu, Dandan, Zhao, Lei, Zhang, Jieying, Chang, Yu, Zhang, Tao, Liu, Hongli
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 27.01.2023
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Summary:Diversity and composition of the gut microbiome are associated with cancer patient outcomes including colorectal cancer (CRC). A growing number of evidence indicates that (Fn) in CRC tissue is associated with worse survival. However, few studies have further analyzed the differences in bacteria in tumor tissues of different patients depending on the survival time of CRC patients. Therefore, there is a need to further explore the bacterial differences in tumor tissues of patients with different prognoses and to identify key bacteria for analysis. Here, we sought to compare the differences in tumor microbiome between patients with long-term survival (LS) longer than 3 years or 4 and 5 years and patients with short-term survival (SS) in the present study cohort. We found that there were significant differences in tumor microbiome between the LS and SS and two bacteria- and -that are present in all of the three groups. Furthermore, by analyzing bacteria in different clinical features, we also found that lower levels of microbiome ( and ) have long-term survival and modulating microbiome in tumor tissue may provide an alternative way to predict the prognosis of CRC patients.
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Edited by: Zhen Dong, Southwest University, China
Reviewed by: Kui Zhang, The University of Chicago, United States; Li Zhang, University of Minnesota Twin Cities, United States
This article was submitted to Gastrointestinal Cancers: Colorectal Cancer, a section of the journal Frontiers in Oncology
ISSN:2234-943X
2234-943X
DOI:10.3389/fonc.2022.1078296