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Eugenol induces apoptosis and inhibits invasion and angiogenesis in a rat model of gastric carcinogenesis induced by MNNG
Combining apoptosis induction with anti-invasive and anti-angiogenic treatment is gaining increasing attention as a promising strategy for cancer chemoprevention. In the present study, eugenol (4-allyl-2-methoxyphenol) was evaluated for its chemopreventive effects on N-methyl-N ′-nitro-N-nitrosoguan...
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Published in: | Life sciences (1973) 2010-06, Vol.86 (25), p.936-941 |
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container_title | Life sciences (1973) |
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creator | Manikandan, Palrasu Murugan, Ramalingam Senthil Priyadarsini, Ramamurthi Vidya Vinothini, Govindarajah Nagini, Siddavaram |
description | Combining apoptosis induction with anti-invasive and anti-angiogenic treatment is gaining increasing attention as a promising strategy for cancer chemoprevention. In the present study, eugenol (4-allyl-2-methoxyphenol) was evaluated for its chemopreventive effects on N-methyl-N
′-nitro-N-nitrosoguanidine (MNNG)-induced gastric carcinogenesis in Wistar rats by analyzing markers of apoptosis, invasion and angiogenesis.
The expressions of markers of apoptosis (Bcl-2, Bcl-xL, Bax, Apaf-1, cytochrome C, caspase-9, caspase-3 and poly(ADP-ribose)polymerase; PARP), invasion (matrix metalloproteinase-2; MMP-2, matrix metalloproteinase-9; MMP-9, reversion-inducing cysteine rich protein with Kazal motifs; RECK and tissue inhibitors of metalloproteinase-2; TIMP-2) and angiogenesis (vascular endothelial growth factor; VEGF and VEGF receptor1; VEGFR1) in stomach tissue of experimental and control animals were measured by gelatin zymogram, immunohistochemical, Western blot and RT-PCR analysis.
Rats administered MNNG developed gastric carcinomas that displayed apoptosis avoidance coupled to upregulation of pro-invasive and angiogenic factors. Administration of eugenol induced apoptosis via the mitochondrial pathway by modulating the Bcl-2 family proteins, Apaf-1, cytochrome C, and caspases and inhibiting invasion, and angiogenesis as evidenced by changes in the activities of MMPs and the expression of MMP-2 and -9, VEGF, VEGFR1, TIMP-2 and RECK.
Phytochemicals such as eugenol that are capable of manipulating the equilibrium between pro- and anti-apoptotic proteins as well as the delicate balance between stimulators and inhibitors of invasion and angiogenesis are attractive candidates for preventing tumour progression. |
doi_str_mv | 10.1016/j.lfs.2010.04.010 |
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′-nitro-N-nitrosoguanidine (MNNG)-induced gastric carcinogenesis in Wistar rats by analyzing markers of apoptosis, invasion and angiogenesis.
The expressions of markers of apoptosis (Bcl-2, Bcl-xL, Bax, Apaf-1, cytochrome C, caspase-9, caspase-3 and poly(ADP-ribose)polymerase; PARP), invasion (matrix metalloproteinase-2; MMP-2, matrix metalloproteinase-9; MMP-9, reversion-inducing cysteine rich protein with Kazal motifs; RECK and tissue inhibitors of metalloproteinase-2; TIMP-2) and angiogenesis (vascular endothelial growth factor; VEGF and VEGF receptor1; VEGFR1) in stomach tissue of experimental and control animals were measured by gelatin zymogram, immunohistochemical, Western blot and RT-PCR analysis.
Rats administered MNNG developed gastric carcinomas that displayed apoptosis avoidance coupled to upregulation of pro-invasive and angiogenic factors. Administration of eugenol induced apoptosis via the mitochondrial pathway by modulating the Bcl-2 family proteins, Apaf-1, cytochrome C, and caspases and inhibiting invasion, and angiogenesis as evidenced by changes in the activities of MMPs and the expression of MMP-2 and -9, VEGF, VEGFR1, TIMP-2 and RECK.
Phytochemicals such as eugenol that are capable of manipulating the equilibrium between pro- and anti-apoptotic proteins as well as the delicate balance between stimulators and inhibitors of invasion and angiogenesis are attractive candidates for preventing tumour progression.</description><identifier>ISSN: 0024-3205</identifier><identifier>EISSN: 1879-0631</identifier><identifier>DOI: 10.1016/j.lfs.2010.04.010</identifier><identifier>PMID: 20434464</identifier><language>eng</language><publisher>Netherlands: Elsevier Inc</publisher><subject>Angiogenesis ; Animals ; Apoptosis ; Apoptosis - drug effects ; Blotting, Western ; Chemoprevention ; Densitometry ; Disease Models, Animal ; Eugenol ; Eugenol - pharmacology ; Gene Expression Regulation, Neoplastic - drug effects ; Immunohistochemistry ; Invasion ; Male ; Matrix Metalloproteinase 2 - genetics ; Matrix Metalloproteinase 2 - metabolism ; Matrix Metalloproteinase 9 - genetics ; Matrix Metalloproteinase 9 - metabolism ; Methylnitronitrosoguanidine ; MNNG ; Neoplasm Invasiveness ; Neoplasm Proteins - genetics ; Neoplasm Proteins - metabolism ; Neovascularization, Pathologic - drug therapy ; Neovascularization, Pathologic - genetics ; Neovascularization, Pathologic - pathology ; Neovascularization, Pathologic - prevention & control ; Rats ; Rats, Wistar ; Reverse Transcriptase Polymerase Chain Reaction ; Stomach Neoplasms - blood supply ; Stomach Neoplasms - chemically induced ; Stomach Neoplasms - genetics ; Stomach Neoplasms - pathology</subject><ispartof>Life sciences (1973), 2010-06, Vol.86 (25), p.936-941</ispartof><rights>2010 Elsevier Inc.</rights><rights>Copyright 2010 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c450t-261bf8aece70522a80b867cb9909573075b12cfc5de9476e44084e121199a0913</citedby><cites>FETCH-LOGICAL-c450t-261bf8aece70522a80b867cb9909573075b12cfc5de9476e44084e121199a0913</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20434464$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Manikandan, Palrasu</creatorcontrib><creatorcontrib>Murugan, Ramalingam Senthil</creatorcontrib><creatorcontrib>Priyadarsini, Ramamurthi Vidya</creatorcontrib><creatorcontrib>Vinothini, Govindarajah</creatorcontrib><creatorcontrib>Nagini, Siddavaram</creatorcontrib><title>Eugenol induces apoptosis and inhibits invasion and angiogenesis in a rat model of gastric carcinogenesis induced by MNNG</title><title>Life sciences (1973)</title><addtitle>Life Sci</addtitle><description>Combining apoptosis induction with anti-invasive and anti-angiogenic treatment is gaining increasing attention as a promising strategy for cancer chemoprevention. In the present study, eugenol (4-allyl-2-methoxyphenol) was evaluated for its chemopreventive effects on N-methyl-N
′-nitro-N-nitrosoguanidine (MNNG)-induced gastric carcinogenesis in Wistar rats by analyzing markers of apoptosis, invasion and angiogenesis.
The expressions of markers of apoptosis (Bcl-2, Bcl-xL, Bax, Apaf-1, cytochrome C, caspase-9, caspase-3 and poly(ADP-ribose)polymerase; PARP), invasion (matrix metalloproteinase-2; MMP-2, matrix metalloproteinase-9; MMP-9, reversion-inducing cysteine rich protein with Kazal motifs; RECK and tissue inhibitors of metalloproteinase-2; TIMP-2) and angiogenesis (vascular endothelial growth factor; VEGF and VEGF receptor1; VEGFR1) in stomach tissue of experimental and control animals were measured by gelatin zymogram, immunohistochemical, Western blot and RT-PCR analysis.
Rats administered MNNG developed gastric carcinomas that displayed apoptosis avoidance coupled to upregulation of pro-invasive and angiogenic factors. Administration of eugenol induced apoptosis via the mitochondrial pathway by modulating the Bcl-2 family proteins, Apaf-1, cytochrome C, and caspases and inhibiting invasion, and angiogenesis as evidenced by changes in the activities of MMPs and the expression of MMP-2 and -9, VEGF, VEGFR1, TIMP-2 and RECK.
Phytochemicals such as eugenol that are capable of manipulating the equilibrium between pro- and anti-apoptotic proteins as well as the delicate balance between stimulators and inhibitors of invasion and angiogenesis are attractive candidates for preventing tumour progression.</description><subject>Angiogenesis</subject><subject>Animals</subject><subject>Apoptosis</subject><subject>Apoptosis - drug effects</subject><subject>Blotting, Western</subject><subject>Chemoprevention</subject><subject>Densitometry</subject><subject>Disease Models, Animal</subject><subject>Eugenol</subject><subject>Eugenol - pharmacology</subject><subject>Gene Expression Regulation, Neoplastic - drug effects</subject><subject>Immunohistochemistry</subject><subject>Invasion</subject><subject>Male</subject><subject>Matrix Metalloproteinase 2 - genetics</subject><subject>Matrix Metalloproteinase 2 - metabolism</subject><subject>Matrix Metalloproteinase 9 - genetics</subject><subject>Matrix Metalloproteinase 9 - metabolism</subject><subject>Methylnitronitrosoguanidine</subject><subject>MNNG</subject><subject>Neoplasm Invasiveness</subject><subject>Neoplasm Proteins - genetics</subject><subject>Neoplasm Proteins - metabolism</subject><subject>Neovascularization, Pathologic - drug therapy</subject><subject>Neovascularization, Pathologic - genetics</subject><subject>Neovascularization, Pathologic - pathology</subject><subject>Neovascularization, Pathologic - prevention & control</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>Stomach Neoplasms - blood supply</subject><subject>Stomach Neoplasms - chemically induced</subject><subject>Stomach Neoplasms - genetics</subject><subject>Stomach Neoplasms - pathology</subject><issn>0024-3205</issn><issn>1879-0631</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNqFkUFP3DAQha0KBFvKD-BS-cYp27EzTmJxQghoJaCX9mw5zmTrVTbe2gnS_nu8LFQ9tacZP31vRp7H2IWApQBRfVkvhz4tJeQ34DKXD2whmloXUJXiiC0AJBalBHXKPqa0BgCl6vKEnUrAErHCBdvdzisaw8D92M2OErfbsJ1C8rkbu6z-8q2fUm6ebfJhfFXtuPIh22iP-azxaCe-CR0NPPR8ZdMUvePORufHv8D9ho63O_749HT_iR33dkh0_lbP2M-72x83X4uH7_ffbq4fCocKpkJWou0bS45qUFLaBtqmql2rNej8GahVK6TrnepIY10RIjRIQgqhtQUtyjN2eZi7jeH3TGkyG58cDYMdKczJ1ApVKVDh_0lsNKIsVSbFgXQxpBSpN9voNzbujACzj8asTY7G7KMxgCaX7Pn8Nn1uN9T9cbxnkYGrA0D5Gs-eoknO05hP5iO5yXTB_2P8C1dYnsE</recordid><startdate>20100619</startdate><enddate>20100619</enddate><creator>Manikandan, Palrasu</creator><creator>Murugan, Ramalingam Senthil</creator><creator>Priyadarsini, Ramamurthi Vidya</creator><creator>Vinothini, Govindarajah</creator><creator>Nagini, Siddavaram</creator><general>Elsevier Inc</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>7X8</scope><scope>7U7</scope><scope>C1K</scope></search><sort><creationdate>20100619</creationdate><title>Eugenol induces apoptosis and inhibits invasion and angiogenesis in a rat model of gastric carcinogenesis induced by MNNG</title><author>Manikandan, Palrasu ; Murugan, Ramalingam Senthil ; Priyadarsini, Ramamurthi Vidya ; Vinothini, Govindarajah ; Nagini, Siddavaram</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c450t-261bf8aece70522a80b867cb9909573075b12cfc5de9476e44084e121199a0913</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Angiogenesis</topic><topic>Animals</topic><topic>Apoptosis</topic><topic>Apoptosis - drug effects</topic><topic>Blotting, Western</topic><topic>Chemoprevention</topic><topic>Densitometry</topic><topic>Disease Models, Animal</topic><topic>Eugenol</topic><topic>Eugenol - pharmacology</topic><topic>Gene Expression Regulation, Neoplastic - drug effects</topic><topic>Immunohistochemistry</topic><topic>Invasion</topic><topic>Male</topic><topic>Matrix Metalloproteinase 2 - genetics</topic><topic>Matrix Metalloproteinase 2 - metabolism</topic><topic>Matrix Metalloproteinase 9 - genetics</topic><topic>Matrix Metalloproteinase 9 - metabolism</topic><topic>Methylnitronitrosoguanidine</topic><topic>MNNG</topic><topic>Neoplasm Invasiveness</topic><topic>Neoplasm Proteins - genetics</topic><topic>Neoplasm Proteins - metabolism</topic><topic>Neovascularization, Pathologic - drug therapy</topic><topic>Neovascularization, Pathologic - genetics</topic><topic>Neovascularization, Pathologic - pathology</topic><topic>Neovascularization, Pathologic - prevention & control</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>Stomach Neoplasms - blood supply</topic><topic>Stomach Neoplasms - chemically induced</topic><topic>Stomach Neoplasms - genetics</topic><topic>Stomach Neoplasms - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Manikandan, Palrasu</creatorcontrib><creatorcontrib>Murugan, Ramalingam Senthil</creatorcontrib><creatorcontrib>Priyadarsini, Ramamurthi Vidya</creatorcontrib><creatorcontrib>Vinothini, Govindarajah</creatorcontrib><creatorcontrib>Nagini, Siddavaram</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Life sciences (1973)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Manikandan, Palrasu</au><au>Murugan, Ramalingam Senthil</au><au>Priyadarsini, Ramamurthi Vidya</au><au>Vinothini, Govindarajah</au><au>Nagini, Siddavaram</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Eugenol induces apoptosis and inhibits invasion and angiogenesis in a rat model of gastric carcinogenesis induced by MNNG</atitle><jtitle>Life sciences (1973)</jtitle><addtitle>Life Sci</addtitle><date>2010-06-19</date><risdate>2010</risdate><volume>86</volume><issue>25</issue><spage>936</spage><epage>941</epage><pages>936-941</pages><issn>0024-3205</issn><eissn>1879-0631</eissn><abstract>Combining apoptosis induction with anti-invasive and anti-angiogenic treatment is gaining increasing attention as a promising strategy for cancer chemoprevention. In the present study, eugenol (4-allyl-2-methoxyphenol) was evaluated for its chemopreventive effects on N-methyl-N
′-nitro-N-nitrosoguanidine (MNNG)-induced gastric carcinogenesis in Wistar rats by analyzing markers of apoptosis, invasion and angiogenesis.
The expressions of markers of apoptosis (Bcl-2, Bcl-xL, Bax, Apaf-1, cytochrome C, caspase-9, caspase-3 and poly(ADP-ribose)polymerase; PARP), invasion (matrix metalloproteinase-2; MMP-2, matrix metalloproteinase-9; MMP-9, reversion-inducing cysteine rich protein with Kazal motifs; RECK and tissue inhibitors of metalloproteinase-2; TIMP-2) and angiogenesis (vascular endothelial growth factor; VEGF and VEGF receptor1; VEGFR1) in stomach tissue of experimental and control animals were measured by gelatin zymogram, immunohistochemical, Western blot and RT-PCR analysis.
Rats administered MNNG developed gastric carcinomas that displayed apoptosis avoidance coupled to upregulation of pro-invasive and angiogenic factors. Administration of eugenol induced apoptosis via the mitochondrial pathway by modulating the Bcl-2 family proteins, Apaf-1, cytochrome C, and caspases and inhibiting invasion, and angiogenesis as evidenced by changes in the activities of MMPs and the expression of MMP-2 and -9, VEGF, VEGFR1, TIMP-2 and RECK.
Phytochemicals such as eugenol that are capable of manipulating the equilibrium between pro- and anti-apoptotic proteins as well as the delicate balance between stimulators and inhibitors of invasion and angiogenesis are attractive candidates for preventing tumour progression.</abstract><cop>Netherlands</cop><pub>Elsevier Inc</pub><pmid>20434464</pmid><doi>10.1016/j.lfs.2010.04.010</doi><tpages>6</tpages></addata></record> |
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subjects | Angiogenesis Animals Apoptosis Apoptosis - drug effects Blotting, Western Chemoprevention Densitometry Disease Models, Animal Eugenol Eugenol - pharmacology Gene Expression Regulation, Neoplastic - drug effects Immunohistochemistry Invasion Male Matrix Metalloproteinase 2 - genetics Matrix Metalloproteinase 2 - metabolism Matrix Metalloproteinase 9 - genetics Matrix Metalloproteinase 9 - metabolism Methylnitronitrosoguanidine MNNG Neoplasm Invasiveness Neoplasm Proteins - genetics Neoplasm Proteins - metabolism Neovascularization, Pathologic - drug therapy Neovascularization, Pathologic - genetics Neovascularization, Pathologic - pathology Neovascularization, Pathologic - prevention & control Rats Rats, Wistar Reverse Transcriptase Polymerase Chain Reaction Stomach Neoplasms - blood supply Stomach Neoplasms - chemically induced Stomach Neoplasms - genetics Stomach Neoplasms - pathology |
title | Eugenol induces apoptosis and inhibits invasion and angiogenesis in a rat model of gastric carcinogenesis induced by MNNG |
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