Multi-cohort analysis reveals colorectal cancer tumor location-associated fecal microbiota and their clinical impact

Yufeng Lin(Chinese University of Hong Kong), Harry Cheuk-Hay Lau(Chinese University of Hong Kong), Chuanfa Liu(Chinese University of Hong Kong), Xiao Ding(Chinese University of Hong Kong), Yang Sun(Kunming Medical University), Jiamei Rong(Kunming Medical University), Xiang Zhang(Chinese University of Hong Kong), Luyao Wang(Chinese University of Hong Kong), Kai Yuan(Chinese University of Hong Kong), Yinglei Miao(Kunming Medical University), William Ka Kei Wu(Chinese University of Hong Kong), Sunny H. Wong(Nanyang Technological University), Joseph J.�Y. Sung(Nanyang Technological University), Jun Yu(Chinese University of Hong Kong)
Cell Host & Microbe
April 1, 2025
Cited by 25Open Access
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Abstract

Microbial alterations in different tumor locations of colorectal cancer (CRC) remain unclear. Here, 1,375 fecal metagenomes from six in-house and published datasets were analyzed, including 128 right-sided CRC (rCRC), 168 left-sided CRC (lCRC), 250 rectal cancer (RC), and 829 controls. Firmicutes progressively increase from rCRC, lCRC, to RC, in contrast to the gradual decrease of Bacteroidetes. Tumor location-associated fecal microbes are identified, including Veillonella parvula for rCRC, Streptococcus angionosus for lCRC, and Peptostreptococcus anaerobius for RC, while Fusobacterium nucleatum is enriched in all tumor locations. Tumor location-associated bacteria correlate with patient survival. Clinically, we establish a microbial biomarker panel for each tumor location that accurately diagnoses rCRC (area under the receiver operating characteristic curve [AUC] = 91.59%), lCRC (AUC = 91.69%), or RC (AUC = 90.53%) from controls. Tumor location-specific biomarkers also have higher diagnostic accuracy (AUC = 91.38%) than location-non-specific biomarkers (AUC = 82.92%). Overall, we characterize fecal microbes associated with different CRC tumor locations, highlighting that tumor location should be considered in non-invasive diagnosis.


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