Unveiling anticancer potential of glibenclamide: Its synergistic cytotoxicity with doxorubicin on cancer cells
[Display omitted] •Glibenclamide interacts with DNA through groove binding.•The spectrometric and electrochemical studies reveal direct interaction of Glibenclamide with DNA.•The interaction between Glibenclamide and B-form of DNA is thermodynamically favorable.•Glibenclamide synergistically enhance...
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creator | Subramaniyam, Nithyananthan Arumugam, Suyavaran Ezthupurakkal, Preedia Babu Ariraman, Subastri Biswas, Indrani Muthuvel, Suresh Kumar Balakrishnan, Aristatile Alshammari, Ghedeir M. Chinnasamy, Thirunavukkarasu |
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•Glibenclamide interacts with DNA through groove binding.•The spectrometric and electrochemical studies reveal direct interaction of Glibenclamide with DNA.•The interaction between Glibenclamide and B-form of DNA is thermodynamically favorable.•Glibenclamide synergistically enhances the cytotoxicity of Doxorubicin against HepG2 and A 549 cells.
Drug repurposing has been an emerging therapeutic strategy, which involves exploration of a new therapeutic approach for the use of an existing drug. Glibenclamide (Gli) is an anti-diabetic sulfonylurea drug extensively used for the treatment of type-2 diabetes, it has also been shown to possess anti-proliferative effect against several types of tumors. The present study was executed to understand the mechanisms underlying the interaction of Gli with DNA under physiological conditions. The binding mechanism of Gli with DNA was scrutinized by UV–vis absorption spectroscopy and fluorescence emission spectroscopy. The conformational changes and electrochemical properties were analyzed by circular dichroism spectroscopy and cyclic voltammetry. Isothermal titration calorimetry was employed to examine the thermodynamic changes and molecular docking technique used to analyze the interaction mode of Gli with DNA. The spectroscopic studies revealed that Gli interacts with DNA through groove binding mode. Further, isothermal titration calorimetry depicted a stronger mode of interaction favorably groove-binding. Recently, systemic combination therapy has shown significant promise in inhibiting multiple targets simultaneously yielding high therapeutic competence with lesser side effects. With this concern, we intended to study the combined cytotoxicity of Gli with doxorubicin (Dox). The results of MTT assay and acridine orange (AO)/ethidium bromide (EtBr) staining showed synergistic cytotoxicity of Gli + Dox combination on HepG2 & A549 cells. The present study documents the intricate mechanism of Gli–DNA interaction and delivers a multifaceted access for chemotherapy by Gli + Dox combination. |
doi_str_mv | 10.1016/j.jpba.2018.03.025 |
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•Glibenclamide interacts with DNA through groove binding.•The spectrometric and electrochemical studies reveal direct interaction of Glibenclamide with DNA.•The interaction between Glibenclamide and B-form of DNA is thermodynamically favorable.•Glibenclamide synergistically enhances the cytotoxicity of Doxorubicin against HepG2 and A 549 cells.
Drug repurposing has been an emerging therapeutic strategy, which involves exploration of a new therapeutic approach for the use of an existing drug. Glibenclamide (Gli) is an anti-diabetic sulfonylurea drug extensively used for the treatment of type-2 diabetes, it has also been shown to possess anti-proliferative effect against several types of tumors. The present study was executed to understand the mechanisms underlying the interaction of Gli with DNA under physiological conditions. The binding mechanism of Gli with DNA was scrutinized by UV–vis absorption spectroscopy and fluorescence emission spectroscopy. The conformational changes and electrochemical properties were analyzed by circular dichroism spectroscopy and cyclic voltammetry. Isothermal titration calorimetry was employed to examine the thermodynamic changes and molecular docking technique used to analyze the interaction mode of Gli with DNA. The spectroscopic studies revealed that Gli interacts with DNA through groove binding mode. Further, isothermal titration calorimetry depicted a stronger mode of interaction favorably groove-binding. Recently, systemic combination therapy has shown significant promise in inhibiting multiple targets simultaneously yielding high therapeutic competence with lesser side effects. With this concern, we intended to study the combined cytotoxicity of Gli with doxorubicin (Dox). The results of MTT assay and acridine orange (AO)/ethidium bromide (EtBr) staining showed synergistic cytotoxicity of Gli + Dox combination on HepG2 & A549 cells. The present study documents the intricate mechanism of Gli–DNA interaction and delivers a multifaceted access for chemotherapy by Gli + Dox combination.</description><identifier>ISSN: 0731-7085</identifier><identifier>EISSN: 1873-264X</identifier><identifier>DOI: 10.1016/j.jpba.2018.03.025</identifier><identifier>PMID: 29567572</identifier><language>eng</language><publisher>England: Elsevier B.V</publisher><subject>A549 Cells ; Anti-cancer ; Antineoplastic Agents - pharmacology ; Calorimetry - methods ; Cell Line, Tumor ; Circular Dichroism - methods ; Combination therapy ; Cytotoxins - pharmacology ; DNA - drug effects ; DNA interaction ; Doxorubicin - pharmacology ; Drug Synergism ; Fluorescence ; Glibenclamide ; Glyburide - pharmacology ; Grove binding ; Hep G2 Cells ; Humans ; Molecular Docking Simulation - methods ; Spectrometry, Fluorescence - methods ; Thermodynamics</subject><ispartof>Journal of pharmaceutical and biomedical analysis, 2018-05, Vol.154, p.294-301</ispartof><rights>2018 Elsevier B.V.</rights><rights>Copyright © 2018 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c356t-195109e22667d0b08c68c5d551f1e891c78a3c9483dc7f6c8ee3362b117e13403</citedby><cites>FETCH-LOGICAL-c356t-195109e22667d0b08c68c5d551f1e891c78a3c9483dc7f6c8ee3362b117e13403</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jpba.2018.03.025$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29567572$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Subramaniyam, Nithyananthan</creatorcontrib><creatorcontrib>Arumugam, Suyavaran</creatorcontrib><creatorcontrib>Ezthupurakkal, Preedia Babu</creatorcontrib><creatorcontrib>Ariraman, Subastri</creatorcontrib><creatorcontrib>Biswas, Indrani</creatorcontrib><creatorcontrib>Muthuvel, Suresh Kumar</creatorcontrib><creatorcontrib>Balakrishnan, Aristatile</creatorcontrib><creatorcontrib>Alshammari, Ghedeir M.</creatorcontrib><creatorcontrib>Chinnasamy, Thirunavukkarasu</creatorcontrib><title>Unveiling anticancer potential of glibenclamide: Its synergistic cytotoxicity with doxorubicin on cancer cells</title><title>Journal of pharmaceutical and biomedical analysis</title><addtitle>J Pharm Biomed Anal</addtitle><description>[Display omitted]
•Glibenclamide interacts with DNA through groove binding.•The spectrometric and electrochemical studies reveal direct interaction of Glibenclamide with DNA.•The interaction between Glibenclamide and B-form of DNA is thermodynamically favorable.•Glibenclamide synergistically enhances the cytotoxicity of Doxorubicin against HepG2 and A 549 cells.
Drug repurposing has been an emerging therapeutic strategy, which involves exploration of a new therapeutic approach for the use of an existing drug. Glibenclamide (Gli) is an anti-diabetic sulfonylurea drug extensively used for the treatment of type-2 diabetes, it has also been shown to possess anti-proliferative effect against several types of tumors. The present study was executed to understand the mechanisms underlying the interaction of Gli with DNA under physiological conditions. The binding mechanism of Gli with DNA was scrutinized by UV–vis absorption spectroscopy and fluorescence emission spectroscopy. The conformational changes and electrochemical properties were analyzed by circular dichroism spectroscopy and cyclic voltammetry. Isothermal titration calorimetry was employed to examine the thermodynamic changes and molecular docking technique used to analyze the interaction mode of Gli with DNA. The spectroscopic studies revealed that Gli interacts with DNA through groove binding mode. Further, isothermal titration calorimetry depicted a stronger mode of interaction favorably groove-binding. Recently, systemic combination therapy has shown significant promise in inhibiting multiple targets simultaneously yielding high therapeutic competence with lesser side effects. With this concern, we intended to study the combined cytotoxicity of Gli with doxorubicin (Dox). The results of MTT assay and acridine orange (AO)/ethidium bromide (EtBr) staining showed synergistic cytotoxicity of Gli + Dox combination on HepG2 & A549 cells. The present study documents the intricate mechanism of Gli–DNA interaction and delivers a multifaceted access for chemotherapy by Gli + Dox combination.</description><subject>A549 Cells</subject><subject>Anti-cancer</subject><subject>Antineoplastic Agents - pharmacology</subject><subject>Calorimetry - methods</subject><subject>Cell Line, Tumor</subject><subject>Circular Dichroism - methods</subject><subject>Combination therapy</subject><subject>Cytotoxins - pharmacology</subject><subject>DNA - drug effects</subject><subject>DNA interaction</subject><subject>Doxorubicin - pharmacology</subject><subject>Drug Synergism</subject><subject>Fluorescence</subject><subject>Glibenclamide</subject><subject>Glyburide - pharmacology</subject><subject>Grove binding</subject><subject>Hep G2 Cells</subject><subject>Humans</subject><subject>Molecular Docking Simulation - methods</subject><subject>Spectrometry, Fluorescence - methods</subject><subject>Thermodynamics</subject><issn>0731-7085</issn><issn>1873-264X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1vEzEQhi0EomnhD3BAPnLZxWOvPxZxQRXQSpW4UImbteudDY42drCdtvn3OCRw5GSN9byvZh5C3gBrgYF6v2k3u3FoOQPTMtEyLp-RFRgtGq66H8_JimkBjWZGXpDLnDeMMQl995Jc8F4qLTVfkXAfHtAvPqzpEIp3Q3CY6C4WrNOw0DjT9eJHDG4Ztn7CD_S2ZJoPAdPa5xqg7lBiiU_e-XKgj778pFN8imk_1p9AY6DnTofLkl-RF_OwZHx9fq_I_ZfP369vmrtvX2-vP901TkhVGuglsB45V0pPbGTGKePkJCXMgKYHp80gXN8ZMTk9K2cQhVB8BNAIomPiirw79e5S_LXHXOzW5-MGQ8C4z_bojIGATlWUn1CXYs4JZ7tLfjukgwVmj57txh49_8lYJmz1XENvz_37cYvTv8hfsRX4eAKwXvngMdnsfLWIk0_oip2i_1__b3pfkDo</recordid><startdate>20180530</startdate><enddate>20180530</enddate><creator>Subramaniyam, Nithyananthan</creator><creator>Arumugam, Suyavaran</creator><creator>Ezthupurakkal, Preedia Babu</creator><creator>Ariraman, Subastri</creator><creator>Biswas, Indrani</creator><creator>Muthuvel, Suresh Kumar</creator><creator>Balakrishnan, Aristatile</creator><creator>Alshammari, Ghedeir M.</creator><creator>Chinnasamy, Thirunavukkarasu</creator><general>Elsevier 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>7X8</scope></search><sort><creationdate>20180530</creationdate><title>Unveiling anticancer potential of glibenclamide: Its synergistic cytotoxicity with doxorubicin on cancer cells</title><author>Subramaniyam, Nithyananthan ; Arumugam, Suyavaran ; Ezthupurakkal, Preedia Babu ; Ariraman, Subastri ; Biswas, Indrani ; Muthuvel, Suresh Kumar ; Balakrishnan, Aristatile ; Alshammari, Ghedeir M. ; Chinnasamy, Thirunavukkarasu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c356t-195109e22667d0b08c68c5d551f1e891c78a3c9483dc7f6c8ee3362b117e13403</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>A549 Cells</topic><topic>Anti-cancer</topic><topic>Antineoplastic Agents - pharmacology</topic><topic>Calorimetry - methods</topic><topic>Cell Line, Tumor</topic><topic>Circular Dichroism - methods</topic><topic>Combination therapy</topic><topic>Cytotoxins - pharmacology</topic><topic>DNA - drug effects</topic><topic>DNA interaction</topic><topic>Doxorubicin - pharmacology</topic><topic>Drug Synergism</topic><topic>Fluorescence</topic><topic>Glibenclamide</topic><topic>Glyburide - pharmacology</topic><topic>Grove binding</topic><topic>Hep G2 Cells</topic><topic>Humans</topic><topic>Molecular Docking Simulation - methods</topic><topic>Spectrometry, Fluorescence - methods</topic><topic>Thermodynamics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Subramaniyam, Nithyananthan</creatorcontrib><creatorcontrib>Arumugam, Suyavaran</creatorcontrib><creatorcontrib>Ezthupurakkal, Preedia Babu</creatorcontrib><creatorcontrib>Ariraman, Subastri</creatorcontrib><creatorcontrib>Biswas, Indrani</creatorcontrib><creatorcontrib>Muthuvel, Suresh Kumar</creatorcontrib><creatorcontrib>Balakrishnan, Aristatile</creatorcontrib><creatorcontrib>Alshammari, Ghedeir M.</creatorcontrib><creatorcontrib>Chinnasamy, Thirunavukkarasu</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><jtitle>Journal of pharmaceutical and biomedical analysis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Subramaniyam, Nithyananthan</au><au>Arumugam, Suyavaran</au><au>Ezthupurakkal, Preedia Babu</au><au>Ariraman, Subastri</au><au>Biswas, Indrani</au><au>Muthuvel, Suresh Kumar</au><au>Balakrishnan, Aristatile</au><au>Alshammari, Ghedeir M.</au><au>Chinnasamy, Thirunavukkarasu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Unveiling anticancer potential of glibenclamide: Its synergistic cytotoxicity with doxorubicin on cancer cells</atitle><jtitle>Journal of pharmaceutical and biomedical analysis</jtitle><addtitle>J Pharm Biomed Anal</addtitle><date>2018-05-30</date><risdate>2018</risdate><volume>154</volume><spage>294</spage><epage>301</epage><pages>294-301</pages><issn>0731-7085</issn><eissn>1873-264X</eissn><abstract>[Display omitted]
•Glibenclamide interacts with DNA through groove binding.•The spectrometric and electrochemical studies reveal direct interaction of Glibenclamide with DNA.•The interaction between Glibenclamide and B-form of DNA is thermodynamically favorable.•Glibenclamide synergistically enhances the cytotoxicity of Doxorubicin against HepG2 and A 549 cells.
Drug repurposing has been an emerging therapeutic strategy, which involves exploration of a new therapeutic approach for the use of an existing drug. Glibenclamide (Gli) is an anti-diabetic sulfonylurea drug extensively used for the treatment of type-2 diabetes, it has also been shown to possess anti-proliferative effect against several types of tumors. The present study was executed to understand the mechanisms underlying the interaction of Gli with DNA under physiological conditions. The binding mechanism of Gli with DNA was scrutinized by UV–vis absorption spectroscopy and fluorescence emission spectroscopy. The conformational changes and electrochemical properties were analyzed by circular dichroism spectroscopy and cyclic voltammetry. Isothermal titration calorimetry was employed to examine the thermodynamic changes and molecular docking technique used to analyze the interaction mode of Gli with DNA. The spectroscopic studies revealed that Gli interacts with DNA through groove binding mode. Further, isothermal titration calorimetry depicted a stronger mode of interaction favorably groove-binding. Recently, systemic combination therapy has shown significant promise in inhibiting multiple targets simultaneously yielding high therapeutic competence with lesser side effects. With this concern, we intended to study the combined cytotoxicity of Gli with doxorubicin (Dox). The results of MTT assay and acridine orange (AO)/ethidium bromide (EtBr) staining showed synergistic cytotoxicity of Gli + Dox combination on HepG2 & A549 cells. The present study documents the intricate mechanism of Gli–DNA interaction and delivers a multifaceted access for chemotherapy by Gli + Dox combination.</abstract><cop>England</cop><pub>Elsevier B.V</pub><pmid>29567572</pmid><doi>10.1016/j.jpba.2018.03.025</doi><tpages>8</tpages></addata></record> |
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subjects | A549 Cells Anti-cancer Antineoplastic Agents - pharmacology Calorimetry - methods Cell Line, Tumor Circular Dichroism - methods Combination therapy Cytotoxins - pharmacology DNA - drug effects DNA interaction Doxorubicin - pharmacology Drug Synergism Fluorescence Glibenclamide Glyburide - pharmacology Grove binding Hep G2 Cells Humans Molecular Docking Simulation - methods Spectrometry, Fluorescence - methods Thermodynamics |
title | Unveiling anticancer potential of glibenclamide: Its synergistic cytotoxicity with doxorubicin on cancer cells |
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