Targeting of cancer cell death mechanisms by resveratrol: a review
Cancer cell death is the utmost aim in cancer therapy. Anti-cancer agents can induce apoptosis, mitotic catastrophe, senescence, or autophagy through the production of free radicals and induction of DNA damage. However, cancer cells can acquire some new properties to adapt to anti-cancer agents. An...
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description | Cancer cell death is the utmost aim in cancer therapy. Anti-cancer agents can induce apoptosis, mitotic catastrophe, senescence, or autophagy through the production of free radicals and induction of DNA damage. However, cancer cells can acquire some new properties to adapt to anti-cancer agents. An increase in the incidence of apoptosis, mitotic catastrophe, senescence, and necrosis is in favor of overcoming tumor resistance to therapy. Although an increase in the autophagy process may help the survival of cancer cells, some studies indicated that stimulation of autophagy cell death may be useful for cancer therapy. Using some low toxic agents to amplify cancer cell death is interesting for the eradication of clonogenic cancer cells. Resveratrol (a polyphenol agent) may affect various signaling pathways related to cell death. It can induce death signals and also downregulate the expression of anti-apoptotic genes. Resveratrol has also been shown to modulate autophagy and induce mitotic catastrophe and senescence in some cancer cells. This review focuses on the important targets and mechanisms for the modulation of cancer cell death by resveratrol. |
doi_str_mv | 10.1007/s10495-021-01689-7 |
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Anti-cancer agents can induce apoptosis, mitotic catastrophe, senescence, or autophagy through the production of free radicals and induction of DNA damage. However, cancer cells can acquire some new properties to adapt to anti-cancer agents. An increase in the incidence of apoptosis, mitotic catastrophe, senescence, and necrosis is in favor of overcoming tumor resistance to therapy. Although an increase in the autophagy process may help the survival of cancer cells, some studies indicated that stimulation of autophagy cell death may be useful for cancer therapy. Using some low toxic agents to amplify cancer cell death is interesting for the eradication of clonogenic cancer cells. Resveratrol (a polyphenol agent) may affect various signaling pathways related to cell death. It can induce death signals and also downregulate the expression of anti-apoptotic genes. Resveratrol has also been shown to modulate autophagy and induce mitotic catastrophe and senescence in some cancer cells. This review focuses on the important targets and mechanisms for the modulation of cancer cell death by resveratrol.</description><identifier>ISSN: 1360-8185</identifier><identifier>EISSN: 1573-675X</identifier><identifier>DOI: 10.1007/s10495-021-01689-7</identifier><identifier>PMID: 34561763</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Anticancer properties ; Antineoplastic Agents - pharmacology ; Antitumor agents ; Apoptosis ; Autophagy ; Biochemistry ; Biomedical and Life Sciences ; Biomedicine ; Cancer ; Cancer Research ; Cancer therapies ; Cell Biology ; Cell death ; DNA damage ; Free radicals ; Gene expression ; Humans ; Mortality ; Necrosis ; Neoplasms - drug therapy ; Neoplasms - genetics ; Oncology ; Phagocytosis ; Resveratrol ; Resveratrol - pharmacology ; Resveratrol - therapeutic use ; Review ; Senescence ; Therapy ; Tumors ; Virology</subject><ispartof>Apoptosis (London), 2021-12, Vol.26 (11-12), p.561-573</ispartof><rights>The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2021</rights><rights>2021. 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Anti-cancer agents can induce apoptosis, mitotic catastrophe, senescence, or autophagy through the production of free radicals and induction of DNA damage. However, cancer cells can acquire some new properties to adapt to anti-cancer agents. An increase in the incidence of apoptosis, mitotic catastrophe, senescence, and necrosis is in favor of overcoming tumor resistance to therapy. Although an increase in the autophagy process may help the survival of cancer cells, some studies indicated that stimulation of autophagy cell death may be useful for cancer therapy. Using some low toxic agents to amplify cancer cell death is interesting for the eradication of clonogenic cancer cells. Resveratrol (a polyphenol agent) may affect various signaling pathways related to cell death. It can induce death signals and also downregulate the expression of anti-apoptotic genes. Resveratrol has also been shown to modulate autophagy and induce mitotic catastrophe and senescence in some cancer cells. This review focuses on the important targets and mechanisms for the modulation of cancer cell death by resveratrol.</description><subject>Anticancer properties</subject><subject>Antineoplastic Agents - pharmacology</subject><subject>Antitumor agents</subject><subject>Apoptosis</subject><subject>Autophagy</subject><subject>Biochemistry</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cancer</subject><subject>Cancer Research</subject><subject>Cancer therapies</subject><subject>Cell Biology</subject><subject>Cell death</subject><subject>DNA damage</subject><subject>Free radicals</subject><subject>Gene expression</subject><subject>Humans</subject><subject>Mortality</subject><subject>Necrosis</subject><subject>Neoplasms - drug therapy</subject><subject>Neoplasms - genetics</subject><subject>Oncology</subject><subject>Phagocytosis</subject><subject>Resveratrol</subject><subject>Resveratrol - pharmacology</subject><subject>Resveratrol - therapeutic use</subject><subject>Review</subject><subject>Senescence</subject><subject>Therapy</subject><subject>Tumors</subject><subject>Virology</subject><issn>1360-8185</issn><issn>1573-675X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kE1PwzAMhiMEYmPwBzigSpwDSdMkDTeY-JImcRkStyjJnK1T146kG9q_J9ABN0625dev7Qehc0quKCHyOlJSKI5JTjGholRYHqAh5ZJhIfnbYcqZILikJR-gkxiXhBBWsuIYDVjBBZWCDdHd1IQ5dFUzz1qfOdM4CJmDus5mYLpFtgK3ME0VVzGzuyxA3EIwXWjrm8ykclvBxyk68qaOcLaPI_T6cD8dP-HJy-Pz-HaCXVHQDheWWseBKVcKkA6EdUwxKhWxUoADxanM8xknXqXbvLdcWuI9z3mujHSGjdBl77sO7fsGYqeX7SY0aaXOuSrL9CwrkirvVS60MQbweh2qlQk7TYn-wqZ7bDph09_YtExDF3vrjV3B7Hfkh1MSsF4QU6uZQ_jb_Y_tJ3Qhd4U</recordid><startdate>20211201</startdate><enddate>20211201</enddate><creator>Fu, Xiao</creator><creator>Li, Mu</creator><creator>Tang, Cuilian</creator><creator>Huang, Zezhi</creator><creator>Najafi, Masoud</creator><general>Springer US</general><general>Springer Nature B.V</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>7QL</scope><scope>7QP</scope><scope>7RQ</scope><scope>7TK</scope><scope>7TM</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>U9A</scope><orcidid>https://orcid.org/0000-0002-6341-9007</orcidid></search><sort><creationdate>20211201</creationdate><title>Targeting of cancer cell death mechanisms by resveratrol: a review</title><author>Fu, Xiao ; Li, Mu ; Tang, Cuilian ; Huang, Zezhi ; Najafi, Masoud</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c441t-4b1bc5e39c86e7ce6bc3931790b76ece951722d50f9617ffb57b0ff52529a7ca3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Anticancer properties</topic><topic>Antineoplastic Agents - pharmacology</topic><topic>Antitumor agents</topic><topic>Apoptosis</topic><topic>Autophagy</topic><topic>Biochemistry</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Cancer</topic><topic>Cancer Research</topic><topic>Cancer therapies</topic><topic>Cell Biology</topic><topic>Cell death</topic><topic>DNA damage</topic><topic>Free radicals</topic><topic>Gene expression</topic><topic>Humans</topic><topic>Mortality</topic><topic>Necrosis</topic><topic>Neoplasms - drug therapy</topic><topic>Neoplasms - genetics</topic><topic>Oncology</topic><topic>Phagocytosis</topic><topic>Resveratrol</topic><topic>Resveratrol - pharmacology</topic><topic>Resveratrol - therapeutic use</topic><topic>Review</topic><topic>Senescence</topic><topic>Therapy</topic><topic>Tumors</topic><topic>Virology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fu, Xiao</creatorcontrib><creatorcontrib>Li, Mu</creatorcontrib><creatorcontrib>Tang, Cuilian</creatorcontrib><creatorcontrib>Huang, Zezhi</creatorcontrib><creatorcontrib>Najafi, Masoud</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>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Career & Technical Education Database</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</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>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</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 Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science 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 Basic</collection><jtitle>Apoptosis (London)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fu, Xiao</au><au>Li, Mu</au><au>Tang, Cuilian</au><au>Huang, Zezhi</au><au>Najafi, Masoud</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Targeting of cancer cell death mechanisms by resveratrol: a review</atitle><jtitle>Apoptosis (London)</jtitle><stitle>Apoptosis</stitle><addtitle>Apoptosis</addtitle><date>2021-12-01</date><risdate>2021</risdate><volume>26</volume><issue>11-12</issue><spage>561</spage><epage>573</epage><pages>561-573</pages><issn>1360-8185</issn><eissn>1573-675X</eissn><abstract>Cancer cell death is the utmost aim in cancer therapy. 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subjects | Anticancer properties Antineoplastic Agents - pharmacology Antitumor agents Apoptosis Autophagy Biochemistry Biomedical and Life Sciences Biomedicine Cancer Cancer Research Cancer therapies Cell Biology Cell death DNA damage Free radicals Gene expression Humans Mortality Necrosis Neoplasms - drug therapy Neoplasms - genetics Oncology Phagocytosis Resveratrol Resveratrol - pharmacology Resveratrol - therapeutic use Review Senescence Therapy Tumors Virology |
title | Targeting of cancer cell death mechanisms by resveratrol: a review |
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