Loading…
Modulation of the tumor microenvironment by microbiota-derived short-chain fatty acids: impact in colorectal cancer therapy
Finding new therapeutic approaches towards colorectal cancer (CRC) is of increased relevance, as CRC is one of the most common cancers worldwide. CRC standard therapy includes surgery, chemotherapy, and radiotherapy, which may be used alone or in combination. The reported side effects and acquired r...
Saved in:
Published in: | International journal of molecular sciences 2023-03, Vol.24 (6), p.1-19 |
---|---|
Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c571t-19063c0ffebeff788f069ddfb06f2f17779b93a7677575f46bb99a76ebb4f60e3 |
---|---|
cites | cdi_FETCH-LOGICAL-c571t-19063c0ffebeff788f069ddfb06f2f17779b93a7677575f46bb99a76ebb4f60e3 |
container_end_page | 19 |
container_issue | 6 |
container_start_page | 1 |
container_title | International journal of molecular sciences |
container_volume | 24 |
creator | Gomes, Sara Rodrigues, Ana Catarina Pazienza, Valerio Preto, Ana |
description | Finding new therapeutic approaches towards colorectal cancer (CRC) is of increased relevance, as CRC is one of the most common cancers worldwide. CRC standard therapy includes surgery, chemotherapy, and radiotherapy, which may be used alone or in combination. The reported side effects and acquired resistance associated with these strategies lead to an increasing need to search for new therapies with better efficacy and less toxicity. Several studies have demonstrated the antitumorigenic properties of microbiota-derived short-chain fatty acids (SCFAs). The tumor microenvironment is composed by non-cellular components, microbiota, and a great diversity of cells, such as immune cells. The influence of SCFAs on the different constituents of the tumor microenvironment is an important issue that should be taken into consideration, and to the best of our knowledge there is a lack of reviews on this subject. The tumor microenvironment is not only closely related to the growth and development of CRC but also affects the treatment and prognosis of the patients. Immunotherapy has emerged as a new hope, but, in CRC, it was found that only a small percentage of patients benefit from this treatment being closely dependent on the genetic background of the tumors. The aim of this review was to perform an up-to-date critical literature review on current knowledge regarding the effects of microbiota-derived SCFAs in the tumor microenvironment, particularly in the context of CRC and its impact in CRC therapeutic strategies. SCFAs, namely acetate, butyrate, and propionate, have the ability to modulate the tumor microenvironment in distinct ways. SCFAs promote immune cell differentiation, downregulate the expression of pro-inflammatory mediators, and restrict the tumor-induced angiogenesis. SCFAs also sustain the integrity of basement membranes and modulate the intestinal pH. CRC patients have lower concentrations of SCFAs than healthy individuals. Increasing the production of SCFAs through the manipulation of the gut microbiota could constitute an important therapeutic strategy towards CRC due to their antitumorigenic effect and ability of modulating tumor microenvironment.
This article is a result of the project EcoAgriFood NORTE-01-0145-FEDER-00009, supported by Norte Portugal Regional Operational Programme (NORTE 2020), under the PORTUGAL 2020 Partnership Agreement, through the European Regional Development Fund (ERDF). Sara Gomes thanks FCT for her PhD grant SFRH/BD/14096 |
doi_str_mv | 10.3390/ijms24065069 |
format | article |
fullrecord | <record><control><sourceid>gale_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_491fd11ace194d1bb5509a68a3244f26</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A751925790</galeid><doaj_id>oai_doaj_org_article_491fd11ace194d1bb5509a68a3244f26</doaj_id><sourcerecordid>A751925790</sourcerecordid><originalsourceid>FETCH-LOGICAL-c571t-19063c0ffebeff788f069ddfb06f2f17779b93a7677575f46bb99a76ebb4f60e3</originalsourceid><addsrcrecordid>eNptkk2PFCEQhjtG466rN8-GxIsHewWahsbLZrPxY5M1XvRMChpmmHQ3I9CTTPzzMva6zhjDAXh56q1UUVX1kuDLppH4nd-MiTLMW8zlo-qcMEprjLl4fHQ-q56ltMGYNrSVT6uzhsuOEsbOq59fQj8PkH2YUHAory3K8xgiGr2JwU47H8M02ikjvV807UOGurfR72yP0jrEXJs1-Ak5yHmPwPg-vUd-3ILJqMgmDCFak2FABiZj4yFLhO3-efXEwZDsi_v9ovr-8cO3m8_13ddPtzfXd7VpBck1kZg3BjtntXVOdJ0rlfa905g76ogQQmrZgOBCtKJ1jGstZblarZnj2DYX1e3i2wfYqG30I8S9CuDVbyHElYKYvRmsYpK4nhAwlkjWE63bFkvgHTSUMUd58bpavLazHm1vSmciDCempy-TX6tV2CmCMes6TIrDm3uHGH7MNmU1-mTsMMBkw5wUFZK2mDFxQF__g27CHKfSqwNFeFv60_ylVlAq8JMLJbE5mKpr0ZLiJiQu1OV_qLJ6W741TNb5op8EvF0Cyp-nFK17KJJgdZg8dTx5BX913JgH-M-oFQAtQDQAWxXtzqcMSZGOUtXxjpHmF3C53-M</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2791655713</pqid></control><display><type>article</type><title>Modulation of the tumor microenvironment by microbiota-derived short-chain fatty acids: impact in colorectal cancer therapy</title><source>PubMed Central database</source><source>ProQuest Publicly Available Content database</source><creator>Gomes, Sara ; Rodrigues, Ana Catarina ; Pazienza, Valerio ; Preto, Ana</creator><creatorcontrib>Gomes, Sara ; Rodrigues, Ana Catarina ; Pazienza, Valerio ; Preto, Ana</creatorcontrib><description>Finding new therapeutic approaches towards colorectal cancer (CRC) is of increased relevance, as CRC is one of the most common cancers worldwide. CRC standard therapy includes surgery, chemotherapy, and radiotherapy, which may be used alone or in combination. The reported side effects and acquired resistance associated with these strategies lead to an increasing need to search for new therapies with better efficacy and less toxicity. Several studies have demonstrated the antitumorigenic properties of microbiota-derived short-chain fatty acids (SCFAs). The tumor microenvironment is composed by non-cellular components, microbiota, and a great diversity of cells, such as immune cells. The influence of SCFAs on the different constituents of the tumor microenvironment is an important issue that should be taken into consideration, and to the best of our knowledge there is a lack of reviews on this subject. The tumor microenvironment is not only closely related to the growth and development of CRC but also affects the treatment and prognosis of the patients. Immunotherapy has emerged as a new hope, but, in CRC, it was found that only a small percentage of patients benefit from this treatment being closely dependent on the genetic background of the tumors. The aim of this review was to perform an up-to-date critical literature review on current knowledge regarding the effects of microbiota-derived SCFAs in the tumor microenvironment, particularly in the context of CRC and its impact in CRC therapeutic strategies. SCFAs, namely acetate, butyrate, and propionate, have the ability to modulate the tumor microenvironment in distinct ways. SCFAs promote immune cell differentiation, downregulate the expression of pro-inflammatory mediators, and restrict the tumor-induced angiogenesis. SCFAs also sustain the integrity of basement membranes and modulate the intestinal pH. CRC patients have lower concentrations of SCFAs than healthy individuals. Increasing the production of SCFAs through the manipulation of the gut microbiota could constitute an important therapeutic strategy towards CRC due to their antitumorigenic effect and ability of modulating tumor microenvironment.
This article is a result of the project EcoAgriFood NORTE-01-0145-FEDER-00009, supported by Norte Portugal Regional Operational Programme (NORTE 2020), under the PORTUGAL 2020 Partnership Agreement, through the European Regional Development Fund (ERDF). Sara Gomes thanks FCT for her PhD grant SFRH/BD/140965/2018. This work was financed by the Portuguese Foundation for Science and Technology (Fundação para a Ciência e a Tecnologia, FCT) within the scope of project PTDC/QUIQIN/28662/2017. This work was also supported by “Contrato-Programa” UIDB/04050/2020 funded by national funds through the FCT I.P.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms24065069</identifier><identifier>PMID: 36982144</identifier><language>eng</language><publisher>Switzerland: Multidisciplinary Digital Publishing Institute (MDPI)</publisher><subject>Acetic acid ; Angiogenesis ; Antimitotic agents ; Antineoplastic agents ; Basement membranes ; Butyrates - pharmacology ; Cancer ; Cancer therapies ; Cell differentiation ; Chemotherapy ; Colorectal cancer ; Colorectal cancer (CRC) ; Colorectal carcinoma ; Colorectal Neoplasms - drug therapy ; Colorectal Neoplasms - metabolism ; Differentiation (biology) ; Drugs ; Fatty acids ; Fatty Acids, Volatile - metabolism ; Gastrointestinal Microbiome ; Health aspects ; Humans ; Immune system ; Immunotherapy ; Inflammation ; Intestinal microflora ; Kinases ; Literature reviews ; Metabolites ; Metastasis ; Microbiota ; Microbiota (Symbiotic organisms) ; Monoclonal antibodies ; Mutation ; Patients ; Radiation therapy ; Review ; Science & Technology ; short-chain fatty acids (SCFAs) ; Therapy ; Toxicity ; Tumor Microenvironment ; Tumors ; Vascular endothelial growth factor</subject><ispartof>International journal of molecular sciences, 2023-03, Vol.24 (6), p.1-19</ispartof><rights>COPYRIGHT 2023 MDPI AG</rights><rights>2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2023 by the authors. 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c571t-19063c0ffebeff788f069ddfb06f2f17779b93a7677575f46bb99a76ebb4f60e3</citedby><cites>FETCH-LOGICAL-c571t-19063c0ffebeff788f069ddfb06f2f17779b93a7677575f46bb99a76ebb4f60e3</cites><orcidid>0000-0002-3492-1153 ; 0000-0002-7302-0630</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2791655713/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2791655713?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36982144$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gomes, Sara</creatorcontrib><creatorcontrib>Rodrigues, Ana Catarina</creatorcontrib><creatorcontrib>Pazienza, Valerio</creatorcontrib><creatorcontrib>Preto, Ana</creatorcontrib><title>Modulation of the tumor microenvironment by microbiota-derived short-chain fatty acids: impact in colorectal cancer therapy</title><title>International journal of molecular sciences</title><addtitle>Int J Mol Sci</addtitle><description>Finding new therapeutic approaches towards colorectal cancer (CRC) is of increased relevance, as CRC is one of the most common cancers worldwide. CRC standard therapy includes surgery, chemotherapy, and radiotherapy, which may be used alone or in combination. The reported side effects and acquired resistance associated with these strategies lead to an increasing need to search for new therapies with better efficacy and less toxicity. Several studies have demonstrated the antitumorigenic properties of microbiota-derived short-chain fatty acids (SCFAs). The tumor microenvironment is composed by non-cellular components, microbiota, and a great diversity of cells, such as immune cells. The influence of SCFAs on the different constituents of the tumor microenvironment is an important issue that should be taken into consideration, and to the best of our knowledge there is a lack of reviews on this subject. The tumor microenvironment is not only closely related to the growth and development of CRC but also affects the treatment and prognosis of the patients. Immunotherapy has emerged as a new hope, but, in CRC, it was found that only a small percentage of patients benefit from this treatment being closely dependent on the genetic background of the tumors. The aim of this review was to perform an up-to-date critical literature review on current knowledge regarding the effects of microbiota-derived SCFAs in the tumor microenvironment, particularly in the context of CRC and its impact in CRC therapeutic strategies. SCFAs, namely acetate, butyrate, and propionate, have the ability to modulate the tumor microenvironment in distinct ways. SCFAs promote immune cell differentiation, downregulate the expression of pro-inflammatory mediators, and restrict the tumor-induced angiogenesis. SCFAs also sustain the integrity of basement membranes and modulate the intestinal pH. CRC patients have lower concentrations of SCFAs than healthy individuals. Increasing the production of SCFAs through the manipulation of the gut microbiota could constitute an important therapeutic strategy towards CRC due to their antitumorigenic effect and ability of modulating tumor microenvironment.
This article is a result of the project EcoAgriFood NORTE-01-0145-FEDER-00009, supported by Norte Portugal Regional Operational Programme (NORTE 2020), under the PORTUGAL 2020 Partnership Agreement, through the European Regional Development Fund (ERDF). Sara Gomes thanks FCT for her PhD grant SFRH/BD/140965/2018. This work was financed by the Portuguese Foundation for Science and Technology (Fundação para a Ciência e a Tecnologia, FCT) within the scope of project PTDC/QUIQIN/28662/2017. This work was also supported by “Contrato-Programa” UIDB/04050/2020 funded by national funds through the FCT I.P.</description><subject>Acetic acid</subject><subject>Angiogenesis</subject><subject>Antimitotic agents</subject><subject>Antineoplastic agents</subject><subject>Basement membranes</subject><subject>Butyrates - pharmacology</subject><subject>Cancer</subject><subject>Cancer therapies</subject><subject>Cell differentiation</subject><subject>Chemotherapy</subject><subject>Colorectal cancer</subject><subject>Colorectal cancer (CRC)</subject><subject>Colorectal carcinoma</subject><subject>Colorectal Neoplasms - drug therapy</subject><subject>Colorectal Neoplasms - metabolism</subject><subject>Differentiation (biology)</subject><subject>Drugs</subject><subject>Fatty acids</subject><subject>Fatty Acids, Volatile - metabolism</subject><subject>Gastrointestinal Microbiome</subject><subject>Health aspects</subject><subject>Humans</subject><subject>Immune system</subject><subject>Immunotherapy</subject><subject>Inflammation</subject><subject>Intestinal microflora</subject><subject>Kinases</subject><subject>Literature reviews</subject><subject>Metabolites</subject><subject>Metastasis</subject><subject>Microbiota</subject><subject>Microbiota (Symbiotic organisms)</subject><subject>Monoclonal antibodies</subject><subject>Mutation</subject><subject>Patients</subject><subject>Radiation therapy</subject><subject>Review</subject><subject>Science & Technology</subject><subject>short-chain fatty acids (SCFAs)</subject><subject>Therapy</subject><subject>Toxicity</subject><subject>Tumor Microenvironment</subject><subject>Tumors</subject><subject>Vascular endothelial growth factor</subject><issn>1422-0067</issn><issn>1661-6596</issn><issn>1422-0067</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkk2PFCEQhjtG466rN8-GxIsHewWahsbLZrPxY5M1XvRMChpmmHQ3I9CTTPzzMva6zhjDAXh56q1UUVX1kuDLppH4nd-MiTLMW8zlo-qcMEprjLl4fHQ-q56ltMGYNrSVT6uzhsuOEsbOq59fQj8PkH2YUHAory3K8xgiGr2JwU47H8M02ikjvV807UOGurfR72yP0jrEXJs1-Ak5yHmPwPg-vUd-3ILJqMgmDCFak2FABiZj4yFLhO3-efXEwZDsi_v9ovr-8cO3m8_13ddPtzfXd7VpBck1kZg3BjtntXVOdJ0rlfa905g76ogQQmrZgOBCtKJ1jGstZblarZnj2DYX1e3i2wfYqG30I8S9CuDVbyHElYKYvRmsYpK4nhAwlkjWE63bFkvgHTSUMUd58bpavLazHm1vSmciDCempy-TX6tV2CmCMes6TIrDm3uHGH7MNmU1-mTsMMBkw5wUFZK2mDFxQF__g27CHKfSqwNFeFv60_ylVlAq8JMLJbE5mKpr0ZLiJiQu1OV_qLJ6W741TNb5op8EvF0Cyp-nFK17KJJgdZg8dTx5BX913JgH-M-oFQAtQDQAWxXtzqcMSZGOUtXxjpHmF3C53-M</recordid><startdate>20230307</startdate><enddate>20230307</enddate><creator>Gomes, Sara</creator><creator>Rodrigues, Ana Catarina</creator><creator>Pazienza, Valerio</creator><creator>Preto, Ana</creator><general>Multidisciplinary Digital Publishing Institute (MDPI)</general><general>MDPI AG</general><general>MDPI</general><scope>RCLKO</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>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</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>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-3492-1153</orcidid><orcidid>https://orcid.org/0000-0002-7302-0630</orcidid></search><sort><creationdate>20230307</creationdate><title>Modulation of the tumor microenvironment by microbiota-derived short-chain fatty acids: impact in colorectal cancer therapy</title><author>Gomes, Sara ; Rodrigues, Ana Catarina ; Pazienza, Valerio ; Preto, Ana</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c571t-19063c0ffebeff788f069ddfb06f2f17779b93a7677575f46bb99a76ebb4f60e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Acetic acid</topic><topic>Angiogenesis</topic><topic>Antimitotic agents</topic><topic>Antineoplastic agents</topic><topic>Basement membranes</topic><topic>Butyrates - pharmacology</topic><topic>Cancer</topic><topic>Cancer therapies</topic><topic>Cell differentiation</topic><topic>Chemotherapy</topic><topic>Colorectal cancer</topic><topic>Colorectal cancer (CRC)</topic><topic>Colorectal carcinoma</topic><topic>Colorectal Neoplasms - drug therapy</topic><topic>Colorectal Neoplasms - metabolism</topic><topic>Differentiation (biology)</topic><topic>Drugs</topic><topic>Fatty acids</topic><topic>Fatty Acids, Volatile - metabolism</topic><topic>Gastrointestinal Microbiome</topic><topic>Health aspects</topic><topic>Humans</topic><topic>Immune system</topic><topic>Immunotherapy</topic><topic>Inflammation</topic><topic>Intestinal microflora</topic><topic>Kinases</topic><topic>Literature reviews</topic><topic>Metabolites</topic><topic>Metastasis</topic><topic>Microbiota</topic><topic>Microbiota (Symbiotic organisms)</topic><topic>Monoclonal antibodies</topic><topic>Mutation</topic><topic>Patients</topic><topic>Radiation therapy</topic><topic>Review</topic><topic>Science & Technology</topic><topic>short-chain fatty acids (SCFAs)</topic><topic>Therapy</topic><topic>Toxicity</topic><topic>Tumor Microenvironment</topic><topic>Tumors</topic><topic>Vascular endothelial growth factor</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gomes, Sara</creatorcontrib><creatorcontrib>Rodrigues, Ana Catarina</creatorcontrib><creatorcontrib>Pazienza, Valerio</creatorcontrib><creatorcontrib>Preto, Ana</creatorcontrib><collection>RCAAP open access repository</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Health and Medical</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Research Library</collection><collection>Research Library (Corporate)</collection><collection>ProQuest Publicly Available Content database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>International journal of molecular sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gomes, Sara</au><au>Rodrigues, Ana Catarina</au><au>Pazienza, Valerio</au><au>Preto, Ana</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Modulation of the tumor microenvironment by microbiota-derived short-chain fatty acids: impact in colorectal cancer therapy</atitle><jtitle>International journal of molecular sciences</jtitle><addtitle>Int J Mol Sci</addtitle><date>2023-03-07</date><risdate>2023</risdate><volume>24</volume><issue>6</issue><spage>1</spage><epage>19</epage><pages>1-19</pages><issn>1422-0067</issn><issn>1661-6596</issn><eissn>1422-0067</eissn><abstract>Finding new therapeutic approaches towards colorectal cancer (CRC) is of increased relevance, as CRC is one of the most common cancers worldwide. CRC standard therapy includes surgery, chemotherapy, and radiotherapy, which may be used alone or in combination. The reported side effects and acquired resistance associated with these strategies lead to an increasing need to search for new therapies with better efficacy and less toxicity. Several studies have demonstrated the antitumorigenic properties of microbiota-derived short-chain fatty acids (SCFAs). The tumor microenvironment is composed by non-cellular components, microbiota, and a great diversity of cells, such as immune cells. The influence of SCFAs on the different constituents of the tumor microenvironment is an important issue that should be taken into consideration, and to the best of our knowledge there is a lack of reviews on this subject. The tumor microenvironment is not only closely related to the growth and development of CRC but also affects the treatment and prognosis of the patients. Immunotherapy has emerged as a new hope, but, in CRC, it was found that only a small percentage of patients benefit from this treatment being closely dependent on the genetic background of the tumors. The aim of this review was to perform an up-to-date critical literature review on current knowledge regarding the effects of microbiota-derived SCFAs in the tumor microenvironment, particularly in the context of CRC and its impact in CRC therapeutic strategies. SCFAs, namely acetate, butyrate, and propionate, have the ability to modulate the tumor microenvironment in distinct ways. SCFAs promote immune cell differentiation, downregulate the expression of pro-inflammatory mediators, and restrict the tumor-induced angiogenesis. SCFAs also sustain the integrity of basement membranes and modulate the intestinal pH. CRC patients have lower concentrations of SCFAs than healthy individuals. Increasing the production of SCFAs through the manipulation of the gut microbiota could constitute an important therapeutic strategy towards CRC due to their antitumorigenic effect and ability of modulating tumor microenvironment.
This article is a result of the project EcoAgriFood NORTE-01-0145-FEDER-00009, supported by Norte Portugal Regional Operational Programme (NORTE 2020), under the PORTUGAL 2020 Partnership Agreement, through the European Regional Development Fund (ERDF). Sara Gomes thanks FCT for her PhD grant SFRH/BD/140965/2018. This work was financed by the Portuguese Foundation for Science and Technology (Fundação para a Ciência e a Tecnologia, FCT) within the scope of project PTDC/QUIQIN/28662/2017. This work was also supported by “Contrato-Programa” UIDB/04050/2020 funded by national funds through the FCT I.P.</abstract><cop>Switzerland</cop><pub>Multidisciplinary Digital Publishing Institute (MDPI)</pub><pmid>36982144</pmid><doi>10.3390/ijms24065069</doi><tpages>19</tpages><orcidid>https://orcid.org/0000-0002-3492-1153</orcidid><orcidid>https://orcid.org/0000-0002-7302-0630</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1422-0067 |
ispartof | International journal of molecular sciences, 2023-03, Vol.24 (6), p.1-19 |
issn | 1422-0067 1661-6596 1422-0067 |
language | eng |
recordid | cdi_doaj_primary_oai_doaj_org_article_491fd11ace194d1bb5509a68a3244f26 |
source | PubMed Central database; ProQuest Publicly Available Content database |
subjects | Acetic acid Angiogenesis Antimitotic agents Antineoplastic agents Basement membranes Butyrates - pharmacology Cancer Cancer therapies Cell differentiation Chemotherapy Colorectal cancer Colorectal cancer (CRC) Colorectal carcinoma Colorectal Neoplasms - drug therapy Colorectal Neoplasms - metabolism Differentiation (biology) Drugs Fatty acids Fatty Acids, Volatile - metabolism Gastrointestinal Microbiome Health aspects Humans Immune system Immunotherapy Inflammation Intestinal microflora Kinases Literature reviews Metabolites Metastasis Microbiota Microbiota (Symbiotic organisms) Monoclonal antibodies Mutation Patients Radiation therapy Review Science & Technology short-chain fatty acids (SCFAs) Therapy Toxicity Tumor Microenvironment Tumors Vascular endothelial growth factor |
title | Modulation of the tumor microenvironment by microbiota-derived short-chain fatty acids: impact in colorectal cancer therapy |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-27T19%3A58%3A51IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Modulation%20of%20the%20tumor%20microenvironment%20by%20microbiota-derived%20short-chain%20fatty%20acids:%20impact%20in%20colorectal%20cancer%20therapy&rft.jtitle=International%20journal%20of%20molecular%20sciences&rft.au=Gomes,%20Sara&rft.date=2023-03-07&rft.volume=24&rft.issue=6&rft.spage=1&rft.epage=19&rft.pages=1-19&rft.issn=1422-0067&rft.eissn=1422-0067&rft_id=info:doi/10.3390/ijms24065069&rft_dat=%3Cgale_doaj_%3EA751925790%3C/gale_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c571t-19063c0ffebeff788f069ddfb06f2f17779b93a7677575f46bb99a76ebb4f60e3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2791655713&rft_id=info:pmid/36982144&rft_galeid=A751925790&rfr_iscdi=true |