Tumor-resident Lactobacillus iners confer chemoradiation resistance through lactate-induced metabolic rewiring

Lauren E. Colbert(The University of Texas MD Anderson Cancer Center), Molly B. El Alam(The University of Texas MD Anderson Cancer Center), Rui Wang(The University of Texas MD Anderson Cancer Center), Tatiana V. Karpinets(The University of Texas MD Anderson Cancer Center), David Lo(The University of Texas MD Anderson Cancer Center), Erica J. Lynn(The University of Texas MD Anderson Cancer Center), Timothy A. Harris(The University of Texas MD Anderson Cancer Center), Jacob H. Elnaggar(Louisiana State University), Kyoko Yoshida-Court(The University of Texas MD Anderson Cancer Center), Katarina Tomasic(The University of Texas MD Anderson Cancer Center), Julianna Bronk(The University of Texas MD Anderson Cancer Center), Julie Sammouri(The University of Texas MD Anderson Cancer Center), Ananta V. Yanamandra(The University of Texas MD Anderson Cancer Center), Adilene Olvera(The University of Texas MD Anderson Cancer Center), Lily G. Carlin(The University of Texas MD Anderson Cancer Center), Travis T. Sims(The University of Texas MD Anderson Cancer Center), Andrea Y. Delgado Medrano(The University of Texas MD Anderson Cancer Center), Tatiana Cisneros Napravnik(The University of Texas MD Anderson Cancer Center), Madison P. O’Hara(The University of Texas MD Anderson Cancer Center), Daniel Lin(The University of Texas MD Anderson Cancer Center), Chike O. Abana(The University of Texas MD Anderson Cancer Center), H. Li(The University of Texas MD Anderson Cancer Center), Patricia J. Eifel(The University of Texas MD Anderson Cancer Center), Anuja Jhingran(The University of Texas MD Anderson Cancer Center), Melissa Joyner(The University of Texas MD Anderson Cancer Center), Lilie L. Lin(The University of Texas MD Anderson Cancer Center), Lois M. Ramondetta(The University of Texas MD Anderson Cancer Center), Andrew M. Futreal(The University of Texas MD Anderson Cancer Center), Kathleen M. Schmeler(The University of Texas MD Anderson Cancer Center), Geena Mathew(The University of Texas MD Anderson Cancer Center), Stephanie Dorta‐Estremera(University of Puerto Rico, Medical Sciences Campus), Jianhua Zhang(The University of Texas MD Anderson Cancer Center), Xiaogang Wu(The University of Texas MD Anderson Cancer Center), Nadim J. Ajami(The University of Texas MD Anderson Cancer Center), Matthew Wong(The University of Texas MD Anderson Cancer Center), Cullen M. Taniguchi(The University of Texas MD Anderson Cancer Center), Joseph F. Petrosino(Baylor College of Medicine), K. Jagannadha Sastry(The University of Texas MD Anderson Cancer Center), Pablo C. Okhuysen(The University of Texas MD Anderson Cancer Center), Sara Martínez(The University of Texas MD Anderson Cancer Center), Lin Tan(The University of Texas MD Anderson Cancer Center), Iqbal Mahmud(The University of Texas MD Anderson Cancer Center), Philip L. Lorenzi(The University of Texas MD Anderson Cancer Center), Jennifer A. Wargo(The University of Texas MD Anderson Cancer Center), Ann H. Klopp(The University of Texas MD Anderson Cancer Center)
Cancer Cell
October 19, 2023
Cited by 229Open Access
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Abstract

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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