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典型文献
Tumorigenic bacteria in colorectal cancer: mechanisms and treatments
文献摘要:
Colorectal cancer (CRC) is the third most common and the second most fatal cancer. In recent years, more attention has been directed toward the role of gut microbiota in the initiation and development of CRC. Some bacterial species, such as Fusobacterium nucleatum, Escherichia coli, Bacteroides fragilis, Enterococcus faecalis, and Salmonella sp. have been associated with CRC, based upon sequencing studies in CRC patients and functional studies in cell culture and animal models. These bacteria can cause host DNA damage by genotoxic substances, including colibactin secreted by pks + Escherichia coli, B. fragilis toxin (BFT) produced by Bacteroides fragilis, and typhoid toxin (TT) from Salmonella. These bacteria can also indirectly promote CRC by influencing host-signaling pathways, such as E-cadherin/β-catenin, TLR4/MYD88/NF-κB, and SMO/RAS/p38 MAPK. Moreover, some of these bacteria can contribute to CRC progression by helping tumor cells to evade the immune response by suppressing immune cell function, creating a pro-inflammatory environment, or influencing the autophagy process. Treatments with the classical antibacterial drugs, metronidazole or erythromycin, the antibacterial active ingredients, M13@ Ag (electrostatically assembled from inorganic silver nanoparticles and the protein capsid of bacteriophage M13), berberine, and zerumbone, were found to inhibit tumorigenic bacteria to different degrees. In this review, we described progress in elucidating the tumorigenic mechanisms of several CRC-associated bacteria, as well as progress in developing effective antibacterial therapies. Specific bacteria have been shown to be active in the oncogenesis and progression of CRC, and some antibacterial compounds have shown therapeutic potential in bacteria-induced CRC. These bacteria may be useful as biomarkers or therapeutic targets for CRC.
文献关键词:
作者姓名:
Sha Li;Jinyi Liu;Xiangjin Zheng;Liwen Ren;Yihui Yang;Wan Li;Weiqi Fu;Jinhua Wang;Guanhua Du
作者机构:
The State Key Laboratory of Bioactive Substance and Function of Natural Medicines,Beijing 100050,China;Key Laboratory of Drug Target Research and Drug Screen,Institute of Materia Medica,Chinese Academy of Medical Science and Peking Union Medical College,Beijing 100050,China
引用格式:
[1]Sha Li;Jinyi Liu;Xiangjin Zheng;Liwen Ren;Yihui Yang;Wan Li;Weiqi Fu;Jinhua Wang;Guanhua Du-.Tumorigenic bacteria in colorectal cancer: mechanisms and treatments)[J].癌症生物学与医学(英文版),2022(02):147-162
A类:
Tumorigenic,colibactin,typhoid,zerumbone
B类:
colorectal,cancer,mechanisms,treatments,Colorectal,CRC,third,most,common,second,fatal,In,recent,years,more,attention,has,been,directed,toward,role,gut,microbiota,initiation,development,Some,species,such,Fusobacterium,nucleatum,Escherichia,Bacteroides,fragilis,Enterococcus,faecalis,Salmonella,have,associated,upon,sequencing,studies,patients,functional,culture,animal,models,These,cause,host,damage,by,genotoxic,substances,including,secreted,pks,toxin,BFT,produced,TT,from,also,indirectly,promote,influencing,signaling,pathways,cadherin,catenin,TLR4,MYD88,SMO,RAS,p38,MAPK,Moreover,some,these,contribute,progression,helping,cells,evade,immune,response,suppressing,creating,inflammatory,environment,autophagy,process,Treatments,classical,antibacterial,drugs,metronidazole,erythromycin,active,ingredients,M13,Ag,electrostatically,assembled,inorganic,silver,nanoparticles,protein,capsid,bacteriophage,berberine,were,found,inhibit,tumorigenic,different,degrees,this,review,described,elucidating,several,well,developing,effective,therapies,Specific,shown,oncogenesis,compounds,therapeutic,potential,induced,may,useful,biomarkers,targets
AB值:
0.578741
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