Potential role of genipin in cancer therapy
[Display omitted] Genipin, an aglycone derived from the iridoid glycoside, geniposide, is isolated and characterized from the extract of Gardenia jasminoides Ellis fruit (family Rubiaceae). It has long been used in traditional oriental medicine for the prevention and treatment of several inflammatio...
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Veröffentlicht in: | Pharmacological research 2018-07, Vol.133, p.195-200 |
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creator | Shanmugam, Muthu K. Shen, Hongyuan Tang, Feng Ru Arfuso, Frank Rajesh, Mohanraj Wang, Lingzhi Kumar, Alan Prem Bian, Jinsong Goh, Boon Cher Bishayee, Anupam Sethi, Gautam |
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Genipin, an aglycone derived from the iridoid glycoside, geniposide, is isolated and characterized from the extract of Gardenia jasminoides Ellis fruit (family Rubiaceae). It has long been used in traditional oriental medicine for the prevention and treatment of several inflammation driven diseases, including cancer. Genipin has been shown to have hepatoprotective activity acting as a potent antioxidant and inhibitor of mitochondrial uncoupling protein 2 (UCP2), and also reported to exert significant anticancer effects. It is an excellent crosslinking agent that helps to make novel sustained or delayed release nanoparticle formulations. In this review, we present the latest developments of genipin as an anticancer agent and briefly describe its diverse mechanism(s) of action. Several lines of evidence suggest that genipin is a potent inhibitor of UCP2, which functions as a tumor promoter in a variety of cancers, attenuates generation of reactive oxygen species and the expression of matrix metalloproteinase 2, as well as induces caspase-dependent apoptosis in vitro and in in vivo models. These finding suggests that genipin can serve as both a prominent anticancer agent as well as a potent crosslinking drug that may find useful application in several novel pharmaceutical formulations. |
doi_str_mv | 10.1016/j.phrs.2018.05.007 |
format | Article |
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Genipin, an aglycone derived from the iridoid glycoside, geniposide, is isolated and characterized from the extract of Gardenia jasminoides Ellis fruit (family Rubiaceae). It has long been used in traditional oriental medicine for the prevention and treatment of several inflammation driven diseases, including cancer. Genipin has been shown to have hepatoprotective activity acting as a potent antioxidant and inhibitor of mitochondrial uncoupling protein 2 (UCP2), and also reported to exert significant anticancer effects. It is an excellent crosslinking agent that helps to make novel sustained or delayed release nanoparticle formulations. In this review, we present the latest developments of genipin as an anticancer agent and briefly describe its diverse mechanism(s) of action. Several lines of evidence suggest that genipin is a potent inhibitor of UCP2, which functions as a tumor promoter in a variety of cancers, attenuates generation of reactive oxygen species and the expression of matrix metalloproteinase 2, as well as induces caspase-dependent apoptosis in vitro and in in vivo models. These finding suggests that genipin can serve as both a prominent anticancer agent as well as a potent crosslinking drug that may find useful application in several novel pharmaceutical formulations.</description><identifier>ISSN: 1043-6618</identifier><identifier>EISSN: 1096-1186</identifier><identifier>DOI: 10.1016/j.phrs.2018.05.007</identifier><identifier>PMID: 29758279</identifier><language>eng</language><publisher>Netherlands: Elsevier Ltd</publisher><subject>Anticancer ; Crosslinking ; Genipin ; Metastasis ; Nano-formulations ; UCP2</subject><ispartof>Pharmacological research, 2018-07, Vol.133, p.195-200</ispartof><rights>2018 Elsevier Ltd</rights><rights>Copyright © 2018 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c422t-6bcba24601bc63d4ef5d9bfe8452390653175a4ca8158be519839172eb2247f53</citedby><cites>FETCH-LOGICAL-c422t-6bcba24601bc63d4ef5d9bfe8452390653175a4ca8158be519839172eb2247f53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1043661817313567$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29758279$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shanmugam, Muthu K.</creatorcontrib><creatorcontrib>Shen, Hongyuan</creatorcontrib><creatorcontrib>Tang, Feng Ru</creatorcontrib><creatorcontrib>Arfuso, Frank</creatorcontrib><creatorcontrib>Rajesh, Mohanraj</creatorcontrib><creatorcontrib>Wang, Lingzhi</creatorcontrib><creatorcontrib>Kumar, Alan Prem</creatorcontrib><creatorcontrib>Bian, Jinsong</creatorcontrib><creatorcontrib>Goh, Boon Cher</creatorcontrib><creatorcontrib>Bishayee, Anupam</creatorcontrib><creatorcontrib>Sethi, Gautam</creatorcontrib><title>Potential role of genipin in cancer therapy</title><title>Pharmacological research</title><addtitle>Pharmacol Res</addtitle><description>[Display omitted]
Genipin, an aglycone derived from the iridoid glycoside, geniposide, is isolated and characterized from the extract of Gardenia jasminoides Ellis fruit (family Rubiaceae). It has long been used in traditional oriental medicine for the prevention and treatment of several inflammation driven diseases, including cancer. Genipin has been shown to have hepatoprotective activity acting as a potent antioxidant and inhibitor of mitochondrial uncoupling protein 2 (UCP2), and also reported to exert significant anticancer effects. It is an excellent crosslinking agent that helps to make novel sustained or delayed release nanoparticle formulations. In this review, we present the latest developments of genipin as an anticancer agent and briefly describe its diverse mechanism(s) of action. Several lines of evidence suggest that genipin is a potent inhibitor of UCP2, which functions as a tumor promoter in a variety of cancers, attenuates generation of reactive oxygen species and the expression of matrix metalloproteinase 2, as well as induces caspase-dependent apoptosis in vitro and in in vivo models. These finding suggests that genipin can serve as both a prominent anticancer agent as well as a potent crosslinking drug that may find useful application in several novel pharmaceutical formulations.</description><subject>Anticancer</subject><subject>Crosslinking</subject><subject>Genipin</subject><subject>Metastasis</subject><subject>Nano-formulations</subject><subject>UCP2</subject><issn>1043-6618</issn><issn>1096-1186</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp9kE1LxDAQhoMo7rr6BzxIj4K0TtIkTcCLLH7Bgh70HNJ06mbptjXpCvvv7bKrR2Fg5vC8L8xDyCWFjAKVt6usX4aYMaAqA5EBFEdkSkHLlFIlj3c3z1MpqZqQsxhXAKA5hVMyYboQihV6Sm7eugHbwdsmCV2DSVcnn9j63rfJOM62DkMyLDHYfntOTmrbRLw47Bn5eHx4nz-ni9enl_n9InWcsSGVpSst4xJo6WRecaxFpcsaFRcs1yBFTgthubOKClWioFrlmhYMS8Z4UYt8Rq73vX3ovjYYB7P20WHT2Ba7TTQMcs1UwZkaUbZHXehiDFibPvi1DVtDwewkmZXZSTI7SQaEGSWNoatD_6ZcY_UX-bUyAnd7AMcvvz0GE53HUUXlA7rBVJ3_r_8HqgZ2fQ</recordid><startdate>201807</startdate><enddate>201807</enddate><creator>Shanmugam, Muthu K.</creator><creator>Shen, Hongyuan</creator><creator>Tang, Feng Ru</creator><creator>Arfuso, Frank</creator><creator>Rajesh, Mohanraj</creator><creator>Wang, Lingzhi</creator><creator>Kumar, Alan Prem</creator><creator>Bian, Jinsong</creator><creator>Goh, Boon Cher</creator><creator>Bishayee, Anupam</creator><creator>Sethi, Gautam</creator><general>Elsevier Ltd</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201807</creationdate><title>Potential role of genipin in cancer therapy</title><author>Shanmugam, Muthu K. ; Shen, Hongyuan ; Tang, Feng Ru ; Arfuso, Frank ; Rajesh, Mohanraj ; Wang, Lingzhi ; Kumar, Alan Prem ; Bian, Jinsong ; Goh, Boon Cher ; Bishayee, Anupam ; Sethi, Gautam</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c422t-6bcba24601bc63d4ef5d9bfe8452390653175a4ca8158be519839172eb2247f53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Anticancer</topic><topic>Crosslinking</topic><topic>Genipin</topic><topic>Metastasis</topic><topic>Nano-formulations</topic><topic>UCP2</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shanmugam, Muthu K.</creatorcontrib><creatorcontrib>Shen, Hongyuan</creatorcontrib><creatorcontrib>Tang, Feng Ru</creatorcontrib><creatorcontrib>Arfuso, Frank</creatorcontrib><creatorcontrib>Rajesh, Mohanraj</creatorcontrib><creatorcontrib>Wang, Lingzhi</creatorcontrib><creatorcontrib>Kumar, Alan Prem</creatorcontrib><creatorcontrib>Bian, Jinsong</creatorcontrib><creatorcontrib>Goh, Boon Cher</creatorcontrib><creatorcontrib>Bishayee, Anupam</creatorcontrib><creatorcontrib>Sethi, Gautam</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Pharmacological research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shanmugam, Muthu K.</au><au>Shen, Hongyuan</au><au>Tang, Feng Ru</au><au>Arfuso, Frank</au><au>Rajesh, Mohanraj</au><au>Wang, Lingzhi</au><au>Kumar, Alan Prem</au><au>Bian, Jinsong</au><au>Goh, Boon Cher</au><au>Bishayee, Anupam</au><au>Sethi, Gautam</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Potential role of genipin in cancer therapy</atitle><jtitle>Pharmacological research</jtitle><addtitle>Pharmacol Res</addtitle><date>2018-07</date><risdate>2018</risdate><volume>133</volume><spage>195</spage><epage>200</epage><pages>195-200</pages><issn>1043-6618</issn><eissn>1096-1186</eissn><abstract>[Display omitted]
Genipin, an aglycone derived from the iridoid glycoside, geniposide, is isolated and characterized from the extract of Gardenia jasminoides Ellis fruit (family Rubiaceae). It has long been used in traditional oriental medicine for the prevention and treatment of several inflammation driven diseases, including cancer. Genipin has been shown to have hepatoprotective activity acting as a potent antioxidant and inhibitor of mitochondrial uncoupling protein 2 (UCP2), and also reported to exert significant anticancer effects. It is an excellent crosslinking agent that helps to make novel sustained or delayed release nanoparticle formulations. In this review, we present the latest developments of genipin as an anticancer agent and briefly describe its diverse mechanism(s) of action. Several lines of evidence suggest that genipin is a potent inhibitor of UCP2, which functions as a tumor promoter in a variety of cancers, attenuates generation of reactive oxygen species and the expression of matrix metalloproteinase 2, as well as induces caspase-dependent apoptosis in vitro and in in vivo models. These finding suggests that genipin can serve as both a prominent anticancer agent as well as a potent crosslinking drug that may find useful application in several novel pharmaceutical formulations.</abstract><cop>Netherlands</cop><pub>Elsevier Ltd</pub><pmid>29758279</pmid><doi>10.1016/j.phrs.2018.05.007</doi><tpages>6</tpages></addata></record> |
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subjects | Anticancer Crosslinking Genipin Metastasis Nano-formulations UCP2 |
title | Potential role of genipin in cancer therapy |
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