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Antioxidant, DNA cleavage, and cellular effects of silibinin and a new oxovanadium(IV)/silibinin complex
A new complex of the oxovanadium(IV) cation with the flavolignan silibinin has been synthesized and characterized. Vanadium compounds show interesting biological and pharmacological properties and some of them display antitumoral actions. Flavonoids are part of a larger group of antioxidant compound...
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Published in: | Journal of biological inorganic chemistry 2011-04, Vol.16 (4), p.653-668 |
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container_title | Journal of biological inorganic chemistry |
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creator | Naso, Luciana G. Ferrer, Evelina G. Butenko, Nataliya Cavaco, Isabel Lezama, Luis Rojo, Teófilo Etcheverry, Susana B. Williams, Patricia A. M. |
description | A new complex of the oxovanadium(IV) cation with the flavolignan silibinin has been synthesized and characterized. Vanadium compounds show interesting biological and pharmacological properties and some of them display antitumoral actions. Flavonoids are part of a larger group of antioxidant compounds called polyphenols which may inhibit the proliferation and growth of cancer cells. The antioxidant and antitumoral effects of silibinin and its oxovanadium(IV) complex were investigated. Silibinin acted as a very strong antioxidant and its complexation with oxovanadium(IV) improved this behavior. Besides, the generation of reactive oxygen species (ROS) by this compound was favored in tumoral (UMR106) cells and correlated with the deleterious behavior in the proliferation of this cell line. Conversely, silibinin did not exert any effect on the proliferation of normal osteoblasts (MC3T3E1). The cytotoxic action and ROS generation of the oxovanadium(IV) complex was more effective in tumoral cells. This behavior was not consistent with cleaving DNA of plasmid DNA pA1 because no significant cleaving activity was observed in both cases. These results suggest that the main deleterious mechanisms may take place through cytotoxic effects more than genotoxic actions. A comparison with our own findings on the behavior of other flavonoids and their vanadyl(IV) complex has also been performed. |
doi_str_mv | 10.1007/s00775-011-0769-8 |
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M.</creator><creatorcontrib>Naso, Luciana G. ; Ferrer, Evelina G. ; Butenko, Nataliya ; Cavaco, Isabel ; Lezama, Luis ; Rojo, Teófilo ; Etcheverry, Susana B. ; Williams, Patricia A. M.</creatorcontrib><description>A new complex of the oxovanadium(IV) cation with the flavolignan silibinin has been synthesized and characterized. Vanadium compounds show interesting biological and pharmacological properties and some of them display antitumoral actions. Flavonoids are part of a larger group of antioxidant compounds called polyphenols which may inhibit the proliferation and growth of cancer cells. The antioxidant and antitumoral effects of silibinin and its oxovanadium(IV) complex were investigated. Silibinin acted as a very strong antioxidant and its complexation with oxovanadium(IV) improved this behavior. Besides, the generation of reactive oxygen species (ROS) by this compound was favored in tumoral (UMR106) cells and correlated with the deleterious behavior in the proliferation of this cell line. Conversely, silibinin did not exert any effect on the proliferation of normal osteoblasts (MC3T3E1). The cytotoxic action and ROS generation of the oxovanadium(IV) complex was more effective in tumoral cells. This behavior was not consistent with cleaving DNA of plasmid DNA pA1 because no significant cleaving activity was observed in both cases. These results suggest that the main deleterious mechanisms may take place through cytotoxic effects more than genotoxic actions. A comparison with our own findings on the behavior of other flavonoids and their vanadyl(IV) complex has also been performed.</description><identifier>ISSN: 0949-8257</identifier><identifier>EISSN: 1432-1327</identifier><identifier>DOI: 10.1007/s00775-011-0769-8</identifier><identifier>PMID: 21399988</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer-Verlag</publisher><subject>Animals ; Antineoplastic Agents - chemical synthesis ; Antineoplastic Agents - chemistry ; Antineoplastic Agents - pharmacology ; Antioxidants - chemical synthesis ; Antioxidants - chemistry ; Antioxidants - pharmacology ; Biochemistry ; Biomedical and Life Sciences ; Cell Line, Tumor ; Cell Proliferation - drug effects ; DNA Cleavage - drug effects ; Dose-Response Relationship, Drug ; Drug Screening Assays, Antitumor ; Electron Spin Resonance Spectroscopy ; Life Sciences ; Microbiology ; Molecular Structure ; Organometallic Compounds - chemical synthesis ; Organometallic Compounds - chemistry ; Organometallic Compounds - pharmacology ; Original Paper ; Plasmids - drug effects ; Rats ; Reactive Oxygen Species - metabolism ; Silymarin - chemistry ; Silymarin - pharmacology ; Spectrophotometry, Ultraviolet ; Spectroscopy, Fourier Transform Infrared ; Structure-Activity Relationship ; Vanadates - chemistry ; Vanadates - pharmacology</subject><ispartof>Journal of biological inorganic chemistry, 2011-04, Vol.16 (4), p.653-668</ispartof><rights>SBIC 2011</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c418t-3937f7f0b586cef3de9dbfbed6827e523f49190af927b9133b4aa14819ff15393</citedby><cites>FETCH-LOGICAL-c418t-3937f7f0b586cef3de9dbfbed6827e523f49190af927b9133b4aa14819ff15393</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21399988$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Naso, Luciana G.</creatorcontrib><creatorcontrib>Ferrer, Evelina G.</creatorcontrib><creatorcontrib>Butenko, Nataliya</creatorcontrib><creatorcontrib>Cavaco, Isabel</creatorcontrib><creatorcontrib>Lezama, Luis</creatorcontrib><creatorcontrib>Rojo, Teófilo</creatorcontrib><creatorcontrib>Etcheverry, Susana B.</creatorcontrib><creatorcontrib>Williams, Patricia A. M.</creatorcontrib><title>Antioxidant, DNA cleavage, and cellular effects of silibinin and a new oxovanadium(IV)/silibinin complex</title><title>Journal of biological inorganic chemistry</title><addtitle>J Biol Inorg Chem</addtitle><addtitle>J Biol Inorg Chem</addtitle><description>A new complex of the oxovanadium(IV) cation with the flavolignan silibinin has been synthesized and characterized. Vanadium compounds show interesting biological and pharmacological properties and some of them display antitumoral actions. Flavonoids are part of a larger group of antioxidant compounds called polyphenols which may inhibit the proliferation and growth of cancer cells. The antioxidant and antitumoral effects of silibinin and its oxovanadium(IV) complex were investigated. Silibinin acted as a very strong antioxidant and its complexation with oxovanadium(IV) improved this behavior. Besides, the generation of reactive oxygen species (ROS) by this compound was favored in tumoral (UMR106) cells and correlated with the deleterious behavior in the proliferation of this cell line. Conversely, silibinin did not exert any effect on the proliferation of normal osteoblasts (MC3T3E1). The cytotoxic action and ROS generation of the oxovanadium(IV) complex was more effective in tumoral cells. This behavior was not consistent with cleaving DNA of plasmid DNA pA1 because no significant cleaving activity was observed in both cases. These results suggest that the main deleterious mechanisms may take place through cytotoxic effects more than genotoxic actions. A comparison with our own findings on the behavior of other flavonoids and their vanadyl(IV) complex has also been performed.</description><subject>Animals</subject><subject>Antineoplastic Agents - chemical synthesis</subject><subject>Antineoplastic Agents - chemistry</subject><subject>Antineoplastic Agents - pharmacology</subject><subject>Antioxidants - chemical synthesis</subject><subject>Antioxidants - chemistry</subject><subject>Antioxidants - pharmacology</subject><subject>Biochemistry</subject><subject>Biomedical and Life Sciences</subject><subject>Cell Line, Tumor</subject><subject>Cell Proliferation - drug effects</subject><subject>DNA Cleavage - drug effects</subject><subject>Dose-Response Relationship, Drug</subject><subject>Drug Screening Assays, Antitumor</subject><subject>Electron Spin Resonance Spectroscopy</subject><subject>Life Sciences</subject><subject>Microbiology</subject><subject>Molecular Structure</subject><subject>Organometallic Compounds - chemical synthesis</subject><subject>Organometallic Compounds - chemistry</subject><subject>Organometallic Compounds - pharmacology</subject><subject>Original Paper</subject><subject>Plasmids - drug effects</subject><subject>Rats</subject><subject>Reactive Oxygen Species - metabolism</subject><subject>Silymarin - chemistry</subject><subject>Silymarin - pharmacology</subject><subject>Spectrophotometry, Ultraviolet</subject><subject>Spectroscopy, Fourier Transform Infrared</subject><subject>Structure-Activity Relationship</subject><subject>Vanadates - chemistry</subject><subject>Vanadates - pharmacology</subject><issn>0949-8257</issn><issn>1432-1327</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNp9kMtOwzAQRS0EoqXwAWyQd4DUUDtO6nhZlVclBBtgaznJuLhK7BInpfw9Li2wYzOWxudeaQ5Cp5RcUUL4yIfB04hQGhE-FlG2h_o0YXFEWcz3UZ-IJCzjlPfQkfcLQghLaXqIejFlQogs66O3iW2NW5tS2XaIrx8nuKhArdQchljZEhdQVV2lGgxaQ9F67DT2pjK5scZ-Ewpb-MBu7VbKqtJ09cXs9XL0xxSuXlawPkYHWlUeTnbvAL3c3jxP76OHp7vZdPIQFQnN2ogJxjXXJE-zcQGalSDKXOdQjrOYQxoznQgqiNIi5rmgjOWJUjTJqNCapiE9QOfb3mXj3jvwrayN31yhLLjOS0GSQKcJDyTdkkXjvG9Ay2VjatV8Skrkxq_c-pXBr9z4lVnInO3au7yG8jfxIzQA8Rbw4cvOoZEL1zU2XPxP6xeawYXk</recordid><startdate>20110401</startdate><enddate>20110401</enddate><creator>Naso, Luciana G.</creator><creator>Ferrer, Evelina G.</creator><creator>Butenko, Nataliya</creator><creator>Cavaco, Isabel</creator><creator>Lezama, Luis</creator><creator>Rojo, Teófilo</creator><creator>Etcheverry, Susana B.</creator><creator>Williams, Patricia A. 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M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Antioxidant, DNA cleavage, and cellular effects of silibinin and a new oxovanadium(IV)/silibinin complex</atitle><jtitle>Journal of biological inorganic chemistry</jtitle><stitle>J Biol Inorg Chem</stitle><addtitle>J Biol Inorg Chem</addtitle><date>2011-04-01</date><risdate>2011</risdate><volume>16</volume><issue>4</issue><spage>653</spage><epage>668</epage><pages>653-668</pages><issn>0949-8257</issn><eissn>1432-1327</eissn><abstract>A new complex of the oxovanadium(IV) cation with the flavolignan silibinin has been synthesized and characterized. Vanadium compounds show interesting biological and pharmacological properties and some of them display antitumoral actions. Flavonoids are part of a larger group of antioxidant compounds called polyphenols which may inhibit the proliferation and growth of cancer cells. The antioxidant and antitumoral effects of silibinin and its oxovanadium(IV) complex were investigated. Silibinin acted as a very strong antioxidant and its complexation with oxovanadium(IV) improved this behavior. Besides, the generation of reactive oxygen species (ROS) by this compound was favored in tumoral (UMR106) cells and correlated with the deleterious behavior in the proliferation of this cell line. Conversely, silibinin did not exert any effect on the proliferation of normal osteoblasts (MC3T3E1). The cytotoxic action and ROS generation of the oxovanadium(IV) complex was more effective in tumoral cells. This behavior was not consistent with cleaving DNA of plasmid DNA pA1 because no significant cleaving activity was observed in both cases. These results suggest that the main deleterious mechanisms may take place through cytotoxic effects more than genotoxic actions. A comparison with our own findings on the behavior of other flavonoids and their vanadyl(IV) complex has also been performed.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer-Verlag</pub><pmid>21399988</pmid><doi>10.1007/s00775-011-0769-8</doi><tpages>16</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Antineoplastic Agents - chemical synthesis Antineoplastic Agents - chemistry Antineoplastic Agents - pharmacology Antioxidants - chemical synthesis Antioxidants - chemistry Antioxidants - pharmacology Biochemistry Biomedical and Life Sciences Cell Line, Tumor Cell Proliferation - drug effects DNA Cleavage - drug effects Dose-Response Relationship, Drug Drug Screening Assays, Antitumor Electron Spin Resonance Spectroscopy Life Sciences Microbiology Molecular Structure Organometallic Compounds - chemical synthesis Organometallic Compounds - chemistry Organometallic Compounds - pharmacology Original Paper Plasmids - drug effects Rats Reactive Oxygen Species - metabolism Silymarin - chemistry Silymarin - pharmacology Spectrophotometry, Ultraviolet Spectroscopy, Fourier Transform Infrared Structure-Activity Relationship Vanadates - chemistry Vanadates - pharmacology |
title | Antioxidant, DNA cleavage, and cellular effects of silibinin and a new oxovanadium(IV)/silibinin complex |
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