Molecular Basis of Resveratrol-Induced Resensitization of Acquired Drug-Resistant Cancer Cells

Multidrug resistance (MDR) to anticancer drugs remains a serious obstacle to the success of cancer chemotherapy. Resveratrol, a polyphenol, present in natural products exerts anticancer activity and acts as a potential MDR inhibitor in various drug-resistant cancer cells. In the process of resensiti...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Nutrients 2022-02, Vol.14 (3), p.699
Hauptverfasser: Choi, Chul Yung, Lim, Sung-Chul, Lee, Tae-Bum, Han, Song Iy
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page
container_issue 3
container_start_page 699
container_title Nutrients
container_volume 14
creator Choi, Chul Yung
Lim, Sung-Chul
Lee, Tae-Bum
Han, Song Iy
description Multidrug resistance (MDR) to anticancer drugs remains a serious obstacle to the success of cancer chemotherapy. Resveratrol, a polyphenol, present in natural products exerts anticancer activity and acts as a potential MDR inhibitor in various drug-resistant cancer cells. In the process of resensitization of drug-resistant cancer cells, resveratrol has been shown to interfere with ABC transporters and drug-metabolizing enzymes, increase DNA damage, inhibit cell cycle progression, and induce apoptosis and autophagy, as well as prevent the induction of epithelial to mesenchymal transition (EMT) and cancer stem cells (CSCs). This review summarizes the mechanisms by which resveratrol counteracts MDR in acquired drug-resistant cancer cell lines and provides a critical basis for understanding the regulation of MDR as well as the development of MDR-inhibiting drugs.
doi_str_mv 10.3390/nu14030699
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8838003</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2627823210</sourcerecordid><originalsourceid>FETCH-LOGICAL-c406t-124b9715e86826212a2fd6ececb2675e70070fa3f8f43c97f773b548547215703</originalsourceid><addsrcrecordid>eNpdkVtLAzEQhYMoKrUv_gBZ8EWE1Vx2k-yLoPUKiiD6akjTWU3ZJppsCvrr3aVVq_Myw8zH4QwHoV2Cjxir8LFLpMAM86paQ9sUC5pzXrD1lXkLDWOc4r4EFpxtoi1WUiFwKbfR851vwKRGh-xMRxszX2cPEOcQdBt8k9-4STIw6Xfgom3tp26tdz12at6TDd3tPKSXvANsbLVrs5F2BkI2gqaJO2ij1k2E4bIP0NPlxePoOr-9v7oZnd7mpsC8zQktxpUgJUguKaeEalpPOBgwY8pFCaK3XmtWy7pgphK1EGxcFrIsBCWlwGyATha6b2k8g4kB1wbdqLdgZzp8KK-t-ntx9lW9-LmSkkmMWSdwsBQI_j1BbNXMRtO9oB34FBXlTAoiaNWj-__QqU_Bde91FBWSMkp6R4cLygQfY4D6xwzBqk9O_SbXwXur9n_Q75zYFx9RkyQ</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2627823210</pqid></control><display><type>article</type><title>Molecular Basis of Resveratrol-Induced Resensitization of Acquired Drug-Resistant Cancer Cells</title><source>MDPI - Multidisciplinary Digital Publishing Institute</source><source>MEDLINE</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><source>PubMed Central Open Access</source><creator>Choi, Chul Yung ; Lim, Sung-Chul ; Lee, Tae-Bum ; Han, Song Iy</creator><creatorcontrib>Choi, Chul Yung ; Lim, Sung-Chul ; Lee, Tae-Bum ; Han, Song Iy</creatorcontrib><description>Multidrug resistance (MDR) to anticancer drugs remains a serious obstacle to the success of cancer chemotherapy. Resveratrol, a polyphenol, present in natural products exerts anticancer activity and acts as a potential MDR inhibitor in various drug-resistant cancer cells. In the process of resensitization of drug-resistant cancer cells, resveratrol has been shown to interfere with ABC transporters and drug-metabolizing enzymes, increase DNA damage, inhibit cell cycle progression, and induce apoptosis and autophagy, as well as prevent the induction of epithelial to mesenchymal transition (EMT) and cancer stem cells (CSCs). This review summarizes the mechanisms by which resveratrol counteracts MDR in acquired drug-resistant cancer cell lines and provides a critical basis for understanding the regulation of MDR as well as the development of MDR-inhibiting drugs.</description><identifier>ISSN: 2072-6643</identifier><identifier>EISSN: 2072-6643</identifier><identifier>DOI: 10.3390/nu14030699</identifier><identifier>PMID: 35277058</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>ABC transporters ; Antitumor activity ; Apoptosis ; Autophagy ; Bladder ; Breast cancer ; Cancer ; Cancer therapies ; Cell cycle ; Chemotherapy ; Colorectal cancer ; DNA damage ; Drug development ; Drug resistance ; Drug Resistance, Multiple ; Drug Resistance, Neoplasm ; Drugs ; Enzymes ; Epithelial-Mesenchymal Transition ; Glycoproteins ; Humans ; Kinases ; Leukemia ; Mesenchyme ; Metabolism ; Multidrug resistance ; Natural products ; Neoplasms - drug therapy ; Neoplasms - metabolism ; Ovaries ; Polyphenols ; Prostate ; Protein expression ; Proteins ; Resveratrol ; Resveratrol - pharmacology ; Review ; Signal transduction ; Stem cells ; Tumor cell lines</subject><ispartof>Nutrients, 2022-02, Vol.14 (3), p.699</ispartof><rights>2022 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>2022 by the authors. 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c406t-124b9715e86826212a2fd6ececb2675e70070fa3f8f43c97f773b548547215703</citedby><cites>FETCH-LOGICAL-c406t-124b9715e86826212a2fd6ececb2675e70070fa3f8f43c97f773b548547215703</cites><orcidid>0000-0003-4975-480X ; 0000-0001-6179-691X ; 0000-0002-2147-0170</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8838003/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8838003/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35277058$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Choi, Chul Yung</creatorcontrib><creatorcontrib>Lim, Sung-Chul</creatorcontrib><creatorcontrib>Lee, Tae-Bum</creatorcontrib><creatorcontrib>Han, Song Iy</creatorcontrib><title>Molecular Basis of Resveratrol-Induced Resensitization of Acquired Drug-Resistant Cancer Cells</title><title>Nutrients</title><addtitle>Nutrients</addtitle><description>Multidrug resistance (MDR) to anticancer drugs remains a serious obstacle to the success of cancer chemotherapy. Resveratrol, a polyphenol, present in natural products exerts anticancer activity and acts as a potential MDR inhibitor in various drug-resistant cancer cells. In the process of resensitization of drug-resistant cancer cells, resveratrol has been shown to interfere with ABC transporters and drug-metabolizing enzymes, increase DNA damage, inhibit cell cycle progression, and induce apoptosis and autophagy, as well as prevent the induction of epithelial to mesenchymal transition (EMT) and cancer stem cells (CSCs). This review summarizes the mechanisms by which resveratrol counteracts MDR in acquired drug-resistant cancer cell lines and provides a critical basis for understanding the regulation of MDR as well as the development of MDR-inhibiting drugs.</description><subject>ABC transporters</subject><subject>Antitumor activity</subject><subject>Apoptosis</subject><subject>Autophagy</subject><subject>Bladder</subject><subject>Breast cancer</subject><subject>Cancer</subject><subject>Cancer therapies</subject><subject>Cell cycle</subject><subject>Chemotherapy</subject><subject>Colorectal cancer</subject><subject>DNA damage</subject><subject>Drug development</subject><subject>Drug resistance</subject><subject>Drug Resistance, Multiple</subject><subject>Drug Resistance, Neoplasm</subject><subject>Drugs</subject><subject>Enzymes</subject><subject>Epithelial-Mesenchymal Transition</subject><subject>Glycoproteins</subject><subject>Humans</subject><subject>Kinases</subject><subject>Leukemia</subject><subject>Mesenchyme</subject><subject>Metabolism</subject><subject>Multidrug resistance</subject><subject>Natural products</subject><subject>Neoplasms - drug therapy</subject><subject>Neoplasms - metabolism</subject><subject>Ovaries</subject><subject>Polyphenols</subject><subject>Prostate</subject><subject>Protein expression</subject><subject>Proteins</subject><subject>Resveratrol</subject><subject>Resveratrol - pharmacology</subject><subject>Review</subject><subject>Signal transduction</subject><subject>Stem cells</subject><subject>Tumor cell lines</subject><issn>2072-6643</issn><issn>2072-6643</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNpdkVtLAzEQhYMoKrUv_gBZ8EWE1Vx2k-yLoPUKiiD6akjTWU3ZJppsCvrr3aVVq_Myw8zH4QwHoV2Cjxir8LFLpMAM86paQ9sUC5pzXrD1lXkLDWOc4r4EFpxtoi1WUiFwKbfR851vwKRGh-xMRxszX2cPEOcQdBt8k9-4STIw6Xfgom3tp26tdz12at6TDd3tPKSXvANsbLVrs5F2BkI2gqaJO2ij1k2E4bIP0NPlxePoOr-9v7oZnd7mpsC8zQktxpUgJUguKaeEalpPOBgwY8pFCaK3XmtWy7pgphK1EGxcFrIsBCWlwGyATha6b2k8g4kB1wbdqLdgZzp8KK-t-ntx9lW9-LmSkkmMWSdwsBQI_j1BbNXMRtO9oB34FBXlTAoiaNWj-__QqU_Bde91FBWSMkp6R4cLygQfY4D6xwzBqk9O_SbXwXur9n_Q75zYFx9RkyQ</recordid><startdate>20220207</startdate><enddate>20220207</enddate><creator>Choi, Chul Yung</creator><creator>Lim, Sung-Chul</creator><creator>Lee, Tae-Bum</creator><creator>Han, Song Iy</creator><general>MDPI AG</general><general>MDPI</general><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>7TS</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</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>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-4975-480X</orcidid><orcidid>https://orcid.org/0000-0001-6179-691X</orcidid><orcidid>https://orcid.org/0000-0002-2147-0170</orcidid></search><sort><creationdate>20220207</creationdate><title>Molecular Basis of Resveratrol-Induced Resensitization of Acquired Drug-Resistant Cancer Cells</title><author>Choi, Chul Yung ; Lim, Sung-Chul ; Lee, Tae-Bum ; Han, Song Iy</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c406t-124b9715e86826212a2fd6ececb2675e70070fa3f8f43c97f773b548547215703</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>ABC transporters</topic><topic>Antitumor activity</topic><topic>Apoptosis</topic><topic>Autophagy</topic><topic>Bladder</topic><topic>Breast cancer</topic><topic>Cancer</topic><topic>Cancer therapies</topic><topic>Cell cycle</topic><topic>Chemotherapy</topic><topic>Colorectal cancer</topic><topic>DNA damage</topic><topic>Drug development</topic><topic>Drug resistance</topic><topic>Drug Resistance, Multiple</topic><topic>Drug Resistance, Neoplasm</topic><topic>Drugs</topic><topic>Enzymes</topic><topic>Epithelial-Mesenchymal Transition</topic><topic>Glycoproteins</topic><topic>Humans</topic><topic>Kinases</topic><topic>Leukemia</topic><topic>Mesenchyme</topic><topic>Metabolism</topic><topic>Multidrug resistance</topic><topic>Natural products</topic><topic>Neoplasms - drug therapy</topic><topic>Neoplasms - metabolism</topic><topic>Ovaries</topic><topic>Polyphenols</topic><topic>Prostate</topic><topic>Protein expression</topic><topic>Proteins</topic><topic>Resveratrol</topic><topic>Resveratrol - pharmacology</topic><topic>Review</topic><topic>Signal transduction</topic><topic>Stem cells</topic><topic>Tumor cell lines</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Choi, Chul Yung</creatorcontrib><creatorcontrib>Lim, Sung-Chul</creatorcontrib><creatorcontrib>Lee, Tae-Bum</creatorcontrib><creatorcontrib>Han, Song Iy</creatorcontrib><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>Physical Education Index</collection><collection>Health &amp; Medical Collection</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>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>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>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Nutrients</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Choi, Chul Yung</au><au>Lim, Sung-Chul</au><au>Lee, Tae-Bum</au><au>Han, Song Iy</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Molecular Basis of Resveratrol-Induced Resensitization of Acquired Drug-Resistant Cancer Cells</atitle><jtitle>Nutrients</jtitle><addtitle>Nutrients</addtitle><date>2022-02-07</date><risdate>2022</risdate><volume>14</volume><issue>3</issue><spage>699</spage><pages>699-</pages><issn>2072-6643</issn><eissn>2072-6643</eissn><abstract>Multidrug resistance (MDR) to anticancer drugs remains a serious obstacle to the success of cancer chemotherapy. Resveratrol, a polyphenol, present in natural products exerts anticancer activity and acts as a potential MDR inhibitor in various drug-resistant cancer cells. In the process of resensitization of drug-resistant cancer cells, resveratrol has been shown to interfere with ABC transporters and drug-metabolizing enzymes, increase DNA damage, inhibit cell cycle progression, and induce apoptosis and autophagy, as well as prevent the induction of epithelial to mesenchymal transition (EMT) and cancer stem cells (CSCs). This review summarizes the mechanisms by which resveratrol counteracts MDR in acquired drug-resistant cancer cell lines and provides a critical basis for understanding the regulation of MDR as well as the development of MDR-inhibiting drugs.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>35277058</pmid><doi>10.3390/nu14030699</doi><orcidid>https://orcid.org/0000-0003-4975-480X</orcidid><orcidid>https://orcid.org/0000-0001-6179-691X</orcidid><orcidid>https://orcid.org/0000-0002-2147-0170</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 2072-6643
ispartof Nutrients, 2022-02, Vol.14 (3), p.699
issn 2072-6643
2072-6643
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8838003
source MDPI - Multidisciplinary Digital Publishing Institute; MEDLINE; EZB-FREE-00999 freely available EZB journals; PubMed Central; PubMed Central Open Access
subjects ABC transporters
Antitumor activity
Apoptosis
Autophagy
Bladder
Breast cancer
Cancer
Cancer therapies
Cell cycle
Chemotherapy
Colorectal cancer
DNA damage
Drug development
Drug resistance
Drug Resistance, Multiple
Drug Resistance, Neoplasm
Drugs
Enzymes
Epithelial-Mesenchymal Transition
Glycoproteins
Humans
Kinases
Leukemia
Mesenchyme
Metabolism
Multidrug resistance
Natural products
Neoplasms - drug therapy
Neoplasms - metabolism
Ovaries
Polyphenols
Prostate
Protein expression
Proteins
Resveratrol
Resveratrol - pharmacology
Review
Signal transduction
Stem cells
Tumor cell lines
title Molecular Basis of Resveratrol-Induced Resensitization of Acquired Drug-Resistant Cancer Cells
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-07T03%3A35%3A25IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Molecular%20Basis%20of%20Resveratrol-Induced%20Resensitization%20of%20Acquired%20Drug-Resistant%20Cancer%20Cells&rft.jtitle=Nutrients&rft.au=Choi,%20Chul%20Yung&rft.date=2022-02-07&rft.volume=14&rft.issue=3&rft.spage=699&rft.pages=699-&rft.issn=2072-6643&rft.eissn=2072-6643&rft_id=info:doi/10.3390/nu14030699&rft_dat=%3Cproquest_pubme%3E2627823210%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2627823210&rft_id=info:pmid/35277058&rfr_iscdi=true