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Role of the Gut Microbiota and Its Metabolites in Tumorigenesis or Development of Colorectal Cancer
Colorectal cancer (CRC) is the most common cancer of the digestive system with high mortality and morbidity rates. Gut microbiota is found in the intestines, especially the colorectum, and has structured crosstalk interactions with the host that affect several physiological processes. The gut microb...
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Published in: | Advanced science 2023-08, Vol.10 (23), p.e2205563-n/a |
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description | Colorectal cancer (CRC) is the most common cancer of the digestive system with high mortality and morbidity rates. Gut microbiota is found in the intestines, especially the colorectum, and has structured crosstalk interactions with the host that affect several physiological processes. The gut microbiota include CRC‐promoting bacterial species, such as Fusobacterium nucleatum, Escherichia coli, and Bacteroides fragilis, and CRC‐protecting bacterial species, such as Clostridium butyricum, Streptococcus thermophilus, and Lacticaseibacillus paracasei, which along with other microorganisms, such as viruses and fungi, play critical roles in the development of CRC. Different bacterial features are identified in patients with early‐onset CRC, combined with different patterns between fecal and intratumoral microbiota. The gut microbiota may be beneficial in the diagnosis and treatment of CRC; some bacteria may serve as biomarkers while others as regulators of chemotherapy and immunotherapy. Furthermore, metabolites produced by the gut microbiota play essential roles in the crosstalk with CRC cells. Harmful metabolites include some primary bile acids and short‐chain fatty acids, whereas others, including ursodeoxycholic acid and butyrate, are beneficial and impede tumor development and progression. This review focuses on the gut microbiota and its metabolites, and their potential roles in the development, diagnosis, and treatment of CRC.
The gut microbiota is associated with colorectal cancer (CRC), and identifying harmful or protective microorganisms and their metabolites in patients is of great significance in the diagnosis and treatment of CRC. Herein, the latest reports on the relationship between gut microbiota and metabolites in CRC and the prospects of treating CRC through targeting these metabolites are summarized and discussed. |
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The gut microbiota is associated with colorectal cancer (CRC), and identifying harmful or protective microorganisms and their metabolites in patients is of great significance in the diagnosis and treatment of CRC. Herein, the latest reports on the relationship between gut microbiota and metabolites in CRC and the prospects of treating CRC through targeting these metabolites are summarized and discussed.</description><identifier>ISSN: 2198-3844</identifier><identifier>EISSN: 2198-3844</identifier><identifier>DOI: 10.1002/advs.202205563</identifier><identifier>PMID: 37263983</identifier><language>eng</language><publisher>Germany: John Wiley & Sons, Inc</publisher><subject>Antigens ; Bacteria ; Carcinogenesis ; Carcinogens ; Cell Transformation, Neoplastic ; Chemokines ; Colorectal cancer ; Colorectal Neoplasms - pathology ; Cytokines ; Escherichia coli ; Fungi ; Gastrointestinal Microbiome - physiology ; gut microbiota ; Humans ; Immune system ; Inflammation ; intratumoral microbiota ; Ligands ; Melanoma ; Metabolism ; metabolite ; Metabolites ; Metastasis ; Microbiota ; Microorganisms ; Mutation ; Pattern recognition ; probiotic bacteria ; Review ; Reviews ; Taxonomy ; Tumorigenesis ; Tumors</subject><ispartof>Advanced science, 2023-08, Vol.10 (23), p.e2205563-n/a</ispartof><rights>2023 The Authors. Advanced Science published by Wiley‐VCH GmbH</rights><rights>2023 The Authors. Advanced Science published by Wiley-VCH GmbH.</rights><rights>2023. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5303-cb8e3569dd25c5f2a9a39ae4601ef64001b005effa40dac560f6460924266a903</citedby><cites>FETCH-LOGICAL-c5303-cb8e3569dd25c5f2a9a39ae4601ef64001b005effa40dac560f6460924266a903</cites><orcidid>0000-0001-5248-7891</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2850875367/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2850875367?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,11562,25753,27924,27925,37012,37013,44590,46052,46476,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37263983$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Qu, Ruize</creatorcontrib><creatorcontrib>Zhang, Yi</creatorcontrib><creatorcontrib>Ma, Yanpeng</creatorcontrib><creatorcontrib>Zhou, Xin</creatorcontrib><creatorcontrib>Sun, Lulu</creatorcontrib><creatorcontrib>Jiang, Changtao</creatorcontrib><creatorcontrib>Zhang, Zhipeng</creatorcontrib><creatorcontrib>Fu, Wei</creatorcontrib><title>Role of the Gut Microbiota and Its Metabolites in Tumorigenesis or Development of Colorectal Cancer</title><title>Advanced science</title><addtitle>Adv Sci (Weinh)</addtitle><description>Colorectal cancer (CRC) is the most common cancer of the digestive system with high mortality and morbidity rates. Gut microbiota is found in the intestines, especially the colorectum, and has structured crosstalk interactions with the host that affect several physiological processes. The gut microbiota include CRC‐promoting bacterial species, such as Fusobacterium nucleatum, Escherichia coli, and Bacteroides fragilis, and CRC‐protecting bacterial species, such as Clostridium butyricum, Streptococcus thermophilus, and Lacticaseibacillus paracasei, which along with other microorganisms, such as viruses and fungi, play critical roles in the development of CRC. Different bacterial features are identified in patients with early‐onset CRC, combined with different patterns between fecal and intratumoral microbiota. The gut microbiota may be beneficial in the diagnosis and treatment of CRC; some bacteria may serve as biomarkers while others as regulators of chemotherapy and immunotherapy. Furthermore, metabolites produced by the gut microbiota play essential roles in the crosstalk with CRC cells. Harmful metabolites include some primary bile acids and short‐chain fatty acids, whereas others, including ursodeoxycholic acid and butyrate, are beneficial and impede tumor development and progression. This review focuses on the gut microbiota and its metabolites, and their potential roles in the development, diagnosis, and treatment of CRC.
The gut microbiota is associated with colorectal cancer (CRC), and identifying harmful or protective microorganisms and their metabolites in patients is of great significance in the diagnosis and treatment of CRC. Herein, the latest reports on the relationship between gut microbiota and metabolites in CRC and the prospects of treating CRC through targeting these metabolites are summarized and discussed.</description><subject>Antigens</subject><subject>Bacteria</subject><subject>Carcinogenesis</subject><subject>Carcinogens</subject><subject>Cell Transformation, Neoplastic</subject><subject>Chemokines</subject><subject>Colorectal cancer</subject><subject>Colorectal Neoplasms - pathology</subject><subject>Cytokines</subject><subject>Escherichia coli</subject><subject>Fungi</subject><subject>Gastrointestinal Microbiome - physiology</subject><subject>gut microbiota</subject><subject>Humans</subject><subject>Immune system</subject><subject>Inflammation</subject><subject>intratumoral microbiota</subject><subject>Ligands</subject><subject>Melanoma</subject><subject>Metabolism</subject><subject>metabolite</subject><subject>Metabolites</subject><subject>Metastasis</subject><subject>Microbiota</subject><subject>Microorganisms</subject><subject>Mutation</subject><subject>Pattern recognition</subject><subject>probiotic bacteria</subject><subject>Review</subject><subject>Reviews</subject><subject>Taxonomy</subject><subject>Tumorigenesis</subject><subject>Tumors</subject><issn>2198-3844</issn><issn>2198-3844</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqFkk1vEzEQQFcIRKvSK0dkiQuXBH_v-oSqFEqkVkhQuFqz3tnUkbMO9m5Q_z0OKVHLhZOtmeenGc9U1WtG54xS_h66XZ5zyjlVSotn1SlnppmJRsrnj-4n1XnOa0opU6KWrHlZnYiaa2EacVq5rzEgiT0Z75BcTSO58S7F1scRCAwdWY6Z3OAIbQx-xEz8QG6nTUx-hQNmn0lM5BJ3GOJ2g8O4Ny1iiAndCIEsYHCYXlUveggZzx_Os-r7p4-3i8-z6y9Xy8XF9cwpQcXMtQ0KpU3XceVUz8GAMIBSU4a9lqX-llKFfQ-SduCUpiWqqeGSaw2GirNqefB2EdZ2m_wG0r2N4O2fQEwrC2n0LqDtgbVtL43utJMGeKNAcRSaQSdYj01xfTi4tlO7wc6V3hKEJ9KnmcHf2VXcWUYlr0VtiuHdgyHFnxPm0W58dhgCDBinbHnDuahrw1lB3_6DruOUhvJXhVK0qZXQdaHmB6oMKOeE_bEaRu1-H-x-H-xxH8qDN497OOJ_p18AeQB--YD3_9HZi8sf35QRQvwGp1jA4Q</recordid><startdate>202308</startdate><enddate>202308</enddate><creator>Qu, Ruize</creator><creator>Zhang, Yi</creator><creator>Ma, Yanpeng</creator><creator>Zhou, Xin</creator><creator>Sun, Lulu</creator><creator>Jiang, Changtao</creator><creator>Zhang, Zhipeng</creator><creator>Fu, Wei</creator><general>John Wiley & Sons, Inc</general><general>John Wiley and Sons Inc</general><general>Wiley</general><scope>24P</scope><scope>WIN</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7XB</scope><scope>88I</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>M2O</scope><scope>M2P</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0001-5248-7891</orcidid></search><sort><creationdate>202308</creationdate><title>Role of the Gut Microbiota and Its Metabolites in Tumorigenesis or Development of Colorectal Cancer</title><author>Qu, Ruize ; 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Gut microbiota is found in the intestines, especially the colorectum, and has structured crosstalk interactions with the host that affect several physiological processes. The gut microbiota include CRC‐promoting bacterial species, such as Fusobacterium nucleatum, Escherichia coli, and Bacteroides fragilis, and CRC‐protecting bacterial species, such as Clostridium butyricum, Streptococcus thermophilus, and Lacticaseibacillus paracasei, which along with other microorganisms, such as viruses and fungi, play critical roles in the development of CRC. Different bacterial features are identified in patients with early‐onset CRC, combined with different patterns between fecal and intratumoral microbiota. The gut microbiota may be beneficial in the diagnosis and treatment of CRC; some bacteria may serve as biomarkers while others as regulators of chemotherapy and immunotherapy. Furthermore, metabolites produced by the gut microbiota play essential roles in the crosstalk with CRC cells. Harmful metabolites include some primary bile acids and short‐chain fatty acids, whereas others, including ursodeoxycholic acid and butyrate, are beneficial and impede tumor development and progression. This review focuses on the gut microbiota and its metabolites, and their potential roles in the development, diagnosis, and treatment of CRC.
The gut microbiota is associated with colorectal cancer (CRC), and identifying harmful or protective microorganisms and their metabolites in patients is of great significance in the diagnosis and treatment of CRC. Herein, the latest reports on the relationship between gut microbiota and metabolites in CRC and the prospects of treating CRC through targeting these metabolites are summarized and discussed.</abstract><cop>Germany</cop><pub>John Wiley & Sons, Inc</pub><pmid>37263983</pmid><doi>10.1002/advs.202205563</doi><tpages>21</tpages><orcidid>https://orcid.org/0000-0001-5248-7891</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Antigens Bacteria Carcinogenesis Carcinogens Cell Transformation, Neoplastic Chemokines Colorectal cancer Colorectal Neoplasms - pathology Cytokines Escherichia coli Fungi Gastrointestinal Microbiome - physiology gut microbiota Humans Immune system Inflammation intratumoral microbiota Ligands Melanoma Metabolism metabolite Metabolites Metastasis Microbiota Microorganisms Mutation Pattern recognition probiotic bacteria Review Reviews Taxonomy Tumorigenesis Tumors |
title | Role of the Gut Microbiota and Its Metabolites in Tumorigenesis or Development of Colorectal Cancer |
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