Gut microbiota imbalance and colorectal cancer

被引:1
作者
Johan Gagnière [1 ,2 ,3 ]
Jennifer Raisch [1 ,2 ,4 ]
Julie Veziant [1 ,2 ,3 ]
Nicolas Barnich [1 ,2 ]
Richard Bonnet [1 ,2 ,5 ]
Emmanuel Buc [1 ,2 ,3 ]
Marie-Agnès Bringer [1 ,2 ,6 ]
Denis Pezet [1 ,2 ,3 ]
Mathilde Bonnet [1 ,2 ]
机构
[1] Clermont Université,UMR 1071 Inserm/Université d’Auvergne
[2] INRA UMR 1324,CNRS UMR 6265,Université de Bourgogne, Centre des Sciences du Go?t et de l’Alimentation, Eye Nutrition and Signalling Research Group
[3] Chirurgie Digestive, Centre Hospitalier Universitaire  4. Laboratoire d’Immunologie, Institut Armand Frappier  5. Bactériologie, Centre Hospital
[4] INRA
关键词
Colorectal cancer; Gut microbiota; Dysbiosis; Cyclomodulin; Oxidative stress;
D O I
暂无
中图分类号
R735.34 [];
学科分类号
100214 ;
摘要
The gut microbiota acts as a real organ. The symbiotic interactions between resident micro-organisms and the digestive tract highly contribute to maintain the gut homeostasis. However, alterations to the microbiome caused by environmental changes(e.g., infection, diet and/or lifestyle) can disturb this symbiotic relationship and promote disease, such as inflammatory bowel diseases and cancer. Colorectal cancer is a complex association of tumoral cells, non-neoplastic cells and a large amount of micro-organisms, and the involvement of the microbiota in colorectal carcinogenesis is becoming increasingly clear. Indeed, many changes in the bacterial composition of the gut microbiota have been reported in colorectal cancer, suggesting a major role of dysbiosis in colorectal carcinogenesis. Some bacterial species have been identified and suspected to play a role in colorectal carcinogenesis, such as Streptococcus bovis, Helicobacter pylori, Bacteroides fragilis, Enterococcus faecalis, Clostridium septicum, Fusobacterium spp. and Escherichia coli. The potential pro-carcinogenic effects of these bacteria are now better understood. In this review, we discuss the possible links between the bacterial microbiota and colorectal carcinogenesis, focusing on dysbiosis and the potential pro-carcinogenic properties of bacteria, such as genotoxicity and other virulence factors, inflammation, host defenses modulation, bacterial derived metabolism, oxidative stress and anti-oxidative defenses modulation. We lastly describe how bacterial microbiota modifications could represent novel prognosis markers and/or targets for innovative therapeutic strategies.
引用
收藏
页码:501 / 518
页数:18
相关论文
共 95 条
[1]  
Colon cancer-associated B2 Escherichia coli colonize gut mucosa and promote cell proliferation[J]. Jennifer Raisch,Emmanuel Buc,Mathilde Bonnet,Pierre Sauvanet,Emilie Vazeille,Amélie de Vallée,Pierre Déchelotte,Claude Darcha,Denis Pezet,Richard Bonnet,Marie-Agnès Bringer,Arlette Darfeuille-Michaud.World Journal of Gastroenterology. 2014(21)
[2]  
Bile acids as endogenous etiologic agents in gastrointestinal cancer[J]. Harris Bernstein,Carol Bernstein,Claire M Payne,Katerina Dvorak.World Journal of Gastroenterology. 2009(27)
[3]  
Microbes, Microbiota, and Colon Cancer[J] . Cynthia L. Sears,Wendy S. Garrett.Cell Host & Microbe . 2014 (3)
[4]   The Multifaceted Role of the Intestinal Microbiota in Colon Cancer [J].
Irrazabal, Thergiory ;
Belcheva, Antoaneta ;
Girardin, Stephen E. ;
Martin, Alberto ;
Philpott, Dana J. .
MOLECULAR CELL, 2014, 54 (02) :309-320
[5]   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
[6]  
Activation of Gpr109a, Receptor for Niacin and the Commensal Metabolite Butyrate, Suppresses Colonic Inflammation and Carcinogenesis[J] . Nagendra Singh,Ashish Gurav,Sathish Sivaprakasam,Evan Brady,Ravi Padia,Huidong Shi,Muthusamy Thangaraju,Puttur D. Prasad,Santhakumar Manicassamy,David H. Munn,Jeffrey R. Lee,Stefan Offermanns,Vadivel Ganapathy.Immunity . 2014 (1)
[7]  
Association between Helicobacter pylori infection and colorectal neoplasm risk: A meta-analysis Based on East Asian population[J] . Yu Guo,Hai-Yan Li.Journal of Cancer Research and Therapeutics . 2014 (8)
[8]   The itinerary of Streptococcus gallolyticus infection in patients with colonic malignant disease [J].
Boleij, Annemarie ;
Tjalsma, Harold .
LANCET INFECTIOUS DISEASES, 2013, 13 (08) :719-724
[9]  
Fusobacterium nucleatum promotes colorectal carcinogenesis by modulating E-cadherin/β-catenin signaling via its FadA adhesin[J] . Mara Roxana Rubinstein,Xiaowei Wang,Wendy Liu,Yujun Hao,Guifang Cai,Yiping W. Han.Cell Host & Microbe . 2013
[10]  
Fusobacterium nucleatum potentiates intestinal tumorigenesis and modulates the tumor immune microenvironment[J] . Aleksandar D. Kostic,Eunyoung Chun,Lauren Robertson,Jonathan N. Glickman,Carey Ann Gallini,Monia Michaud,Thomas E. Clancy,Daniel C. Chung,Paul Lochhead,Georgina L. Hold,Emad M. El-Omar,Dean Brenner,Charles S. Fuchs,Matthew Meyerson,Wendy S. Garrett.Cell Host & Microbe . 2013