Gut Microbiota Influences Experimental Outcomes in Mouse Models of Colorectal Cancer

被引:42
作者
Leystra, Alyssa A. [1 ]
Clapper, Margie L. [1 ]
机构
[1] Fox Chase Canc Ctr, Canc Prevent & Control Program, Philadelphia, PA 19111 USA
关键词
colorectal cancer; mouse models; microbiota; antitumor immunity; REGULATORY T-CELLS; COLITIS-ASSOCIATED CARCINOGENESIS; HELICOBACTER-HEPATICUS; COLON TUMORIGENESIS; FATTY-ACIDS; IMMUNITY; MICE; IMMUNOTHERAPY; DISEASE; FLORA;
D O I
10.3390/genes10110900
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Colorectal cancer (CRC) is a leading cause of cancer-related deaths worldwide. Mouse models are a valuable resource for use throughout the development and testing of new therapeutic strategies for CRC. Tumorigenesis and response to therapy in humans and mouse models alike are influenced by the microbial communities that colonize the gut. Differences in the composition of the gut microbiota can confound experimental findings and reduce the replicability and translatability of the resulting data. Despite this, the contribution of resident microbiota to preclinical tumor models is often underappreciated. This review does the following: (1) summarizes evidence that the gut microbiota influence CRC disease phenotypes; (2) outlines factors that can influence the composition of the gut microbiota; and (3) provides strategies that can be incorporated into the experimental design, to account for the influence of the microbiota on intestinal phenotypes in mouse models of CRC. Through careful experimental design and documentation, mouse models can continue to rapidly advance efforts to prevent and treat colon cancer.
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页数:20
相关论文
共 97 条
[1]   Quantitative PCR assays for mouse enteric flora reveal strain-dependent differences in composition that are influenced by the microenvironment [J].
Alexander, A. Deloris ;
Orcutt, Roger P. ;
Henry, JaNell C. ;
Baker, Joseph ;
Bissahoyo, Anika C. ;
Threadgill, David W. .
MAMMALIAN GENOME, 2006, 17 (11) :1093-1104
[2]   Emerging Technologies for Gut Microbiome Research [J].
Arnold, Jason W. ;
Roach, Jeffrey ;
Azcarate-Peril, M. Andrea .
TRENDS IN MICROBIOLOGY, 2016, 24 (11) :887-901
[3]   Microbial genomic analysis reveals the essential role of inflammation in bacteria-induced colorectal cancer [J].
Arthur, Janelle C. ;
Gharaibeh, Raad Z. ;
Muehlbauer, Marcus ;
Perez-Chanona, Ernesto ;
Uronis, Joshua M. ;
McCafferty, Jonathan ;
Fodor, Anthony A. ;
Jobin, Christian .
NATURE COMMUNICATIONS, 2014, 5
[4]   Intestinal Inflammation Targets Cancer-Inducing Activity of the Microbiota [J].
Arthur, Janelle C. ;
Perez-Chanona, Ernesto ;
Muehlbauer, Marcus ;
Tomkovich, Sarah ;
Uronis, Joshua M. ;
Fan, Ting-Jia ;
Campbell, Barry J. ;
Abujamel, Turki ;
Dogan, Belgin ;
Rogers, Arlin B. ;
Rhodes, Jonathan M. ;
Stintzi, Alain ;
Simpson, Kenneth W. ;
Hansen, Jonathan J. ;
Keku, Temitope O. ;
Fodor, Anthony A. ;
Jobin, Christian .
SCIENCE, 2012, 338 (6103) :120-123
[5]   Treg induction by a rationally selected mixture of Clostridia strains from the human microbiota [J].
Atarashi, Koji ;
Tanoue, Takeshi ;
Oshima, Kenshiro ;
Suda, Wataru ;
Nagano, Yuji ;
Nishikawa, Hiroyoshi ;
Fukuda, Shinji ;
Saito, Takuro ;
Narushima, Seiko ;
Hase, Koji ;
Kim, Sangwan ;
Fritz, Joelle V. ;
Wilmes, Paul ;
Ueha, Satoshi ;
Matsushima, Kouji ;
Ohno, Hiroshi ;
Olle, Bernat ;
Sakaguchi, Shimon ;
Taniguchi, Tadatsugu ;
Morita, Hidetoshi ;
Hattori, Masahira ;
Honda, Kenya .
NATURE, 2013, 500 (7461) :232-+
[6]   Induction of Colonic Regulatory T Cells by Indigenous Clostridium Species [J].
Atarashi, Koji ;
Tanoue, Takeshi ;
Shima, Tatsuichiro ;
Imaoka, Akemi ;
Kuwahara, Tomomi ;
Momose, Yoshika ;
Cheng, Genhong ;
Yamasaki, Sho ;
Saito, Takashi ;
Ohba, Yusuke ;
Taniguchi, Tadatsugu ;
Takeda, Kiyoshi ;
Hori, Shohei ;
Ivanov, Ivaylo I. ;
Umesaki, Yoshinori ;
Itoh, Kikuji ;
Honda, Kenya .
SCIENCE, 2011, 331 (6015) :337-341
[7]   Refinement of Experimental Design and Conduct in Laboratory Animal Research [J].
Bailoo, Jeremy D. ;
Reichlin, Thomas S. ;
Wuerbel, Hanno .
ILAR JOURNAL, 2014, 55 (03) :383-391
[8]  
BAUER H, 1963, AM J PATHOL, V42, P471
[9]   Gut Microbial Metabolism Drives Transformation of Msh2-Deficient Colon Epithelial Cells [J].
Belcheva, Antoaneta ;
Irrazabal, Thergiory ;
Robertson, Susan J. ;
Streutker, Catherine ;
Maughan, Heather ;
Rubino, Stephen ;
Moriyama, Eduardo H. ;
Copeland, Julia K. ;
Kumar, Sachin ;
Green, Blerta ;
Geddes, Kaoru ;
Pezo, Rossanna C. ;
Navarre, William W. ;
Milosevic, Michael ;
Wilson, Brian C. ;
Girardin, Stephen E. ;
Wolever, Thomas M. S. ;
Edelmann, Winfried ;
Guttman, David S. ;
Philpott, Dana J. ;
Martin, Alberto .
CELL, 2014, 158 (02) :288-299
[10]   Individuality in gut microbiota composition is a complex polygenic trait shaped by multiple environmental and host genetic factors [J].
Benson, Andrew K. ;
Kelly, Scott A. ;
Legge, Ryan ;
Ma, Fangrui ;
Low, Soo Jen ;
Kim, Jaehyoung ;
Zhang, Min ;
Oh, Phaik Lyn ;
Nehrenberg, Derrick ;
Hua, Kunjie ;
Kachman, Stephen D. ;
Moriyama, Etsuko N. ;
Walter, Jens ;
Peterson, Daniel A. ;
Pomp, Daniel .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2010, 107 (44) :18933-18938