乳酸
生物
癌症研究
免疫系统
结直肠癌
细菌
肿瘤微环境
癌细胞
微生物群
代谢途径
新陈代谢
癌症
微生物学
免疫学
生物化学
生物信息学
遗传学
作者
Lauren E. Colbert,Molly B. El Alam,Rui Wang,Tatiana V. Karpinets,David Lo,Erica J. Lynn,Timothy A. Harris,Jacob H. Elnaggar,Kyoko Yoshida-Court,Katarina Tomasic,Julianna Bronk,Julie Sammouri,Ananta V. Yanamandra,Adilene Olvera,Lily G. Carlin,Travis T. Sims,Andrea Y. Delgado Medrano,Tatiana Cisneros Napravnik,Madison P. O’Hara,Daniel Lin
出处
期刊:Cancer Cell
[Cell Press]
日期:2023-10-19
卷期号:41 (11): 1945-1962.e11
被引量:247
标识
DOI:10.1016/j.ccell.2023.09.012
摘要
Tumor microbiota can produce active metabolites that affect cancer and immune cell signaling, metabolism, and proliferation. Here, we explore tumor and gut microbiome features that affect chemoradiation response in patients with cervical cancer using a combined approach of deep microbiome sequencing, targeted bacterial culture, and in vitro assays. We identify that an obligate L-lactate-producing lactic acid bacterium found in tumors, Lactobacillus iners, is associated with decreased survival in patients, induces chemotherapy and radiation resistance in cervical cancer cells, and leads to metabolic rewiring, or alterations in multiple metabolic pathways, in tumors. Genomically similar L-lactate-producing lactic acid bacteria commensal to other body sites are also significantly associated with survival in colorectal, lung, head and neck, and skin cancers. Our findings demonstrate that lactic acid bacteria in the tumor microenvironment can alter tumor metabolism and lactate signaling pathways, causing therapeutic resistance. Lactic acid bacteria could be promising therapeutic targets across cancer types.
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