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Effect of Arylazo Sulfones on DNA: Binding, Cleavage, Photocleavage, Molecular Docking Studies and Interaction with A375 Melanoma and Non-Cancer Cells
A set of arylazo sulfones, known to undergo N-S bond cleavage upon light exposure, has been synthesized, and their activity in the dark and upon irradiation towards DNA has been investigated. Their interaction with calf-thymus DNA has been examined, and the significant affinity observed (most probab...
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Published in: | International journal of molecular sciences 2023-01, Vol.24 (3), p.1834 |
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creator | Mikra, Chrysoula Mitrakas, Achilleas Ghizzani, Virginia Katsani, Katerina R Koffa, Maria Koukourakis, Michael Psomas, George Protti, Stefano Fagnoni, Maurizio Fylaktakidou, Konstantina C |
description | A set of arylazo sulfones, known to undergo N-S bond cleavage upon light exposure, has been synthesized, and their activity in the dark and upon irradiation towards DNA has been investigated. Their interaction with calf-thymus DNA has been examined, and the significant affinity observed (most probably due to DNA intercalation) was analyzed by means of molecular docking "in silico" calculations that pointed out polar contacts, mainly via the sulfonyl moiety. Incubation with plasmid pBluescript KS II revealed DNA cleavage that has been studied over time and concentration. UV-A irradiation considerably improved DNA damage for most of the compounds, whereas under visible light the effect was slightly lower. Moving to in vitro experiments, irradiation was found to slightly enhance the death of the cells in the majority of the compounds. Naphthylazosulfone
showed photo-disruptive effect under UV-A irradiation (IC
~13 μΜ) followed by derivatives
and
(IC
~100 μΜ). Those compounds were irradiated in the presence of two non-cancer cell lines and were found equally toxic only upon irradiation and not in the dark. The temporal and spatial control of light, therefore, might provide a chance for these novel scaffolds to be useful for the development of phototoxic pharmaceuticals. |
doi_str_mv | 10.3390/ijms24031834 |
format | article |
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showed photo-disruptive effect under UV-A irradiation (IC
~13 μΜ) followed by derivatives
and
(IC
~100 μΜ). Those compounds were irradiated in the presence of two non-cancer cell lines and were found equally toxic only upon irradiation and not in the dark. The temporal and spatial control of light, therefore, might provide a chance for these novel scaffolds to be useful for the development of phototoxic pharmaceuticals.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms24031834</identifier><identifier>PMID: 36768159</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Cancer therapies ; Cell death ; Chemotherapy ; Cleavage ; Deoxyribonucleic acid ; DNA ; DNA - chemistry ; DNA Cleavage ; DNA damage ; Experiments ; Fluorides ; Humans ; Light ; Light effects ; Melanoma ; Molecular docking ; Molecular Docking Simulation ; Nitrogen ; Photodynamic therapy ; Radiation damage ; Sulfones ; Sulfones - pharmacology ; Thymus gland ; Tumor cell lines ; Ultraviolet Rays ; Viscosity</subject><ispartof>International journal of molecular sciences, 2023-01, Vol.24 (3), p.1834</ispartof><rights>2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2023 by the authors. 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c412t-703265ad6046225656f002da130dbb43edcf217c2da0730e5fec01d820ddf06d3</citedby><cites>FETCH-LOGICAL-c412t-703265ad6046225656f002da130dbb43edcf217c2da0730e5fec01d820ddf06d3</cites><orcidid>0000-0002-5879-7265 ; 0000-0003-0247-7585 ; 0000-0002-9980-7773 ; 0000-0002-2186-2617 ; 0000-0002-5313-5692</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2774922278/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2774922278?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25731,27901,27902,36989,36990,44566,53766,53768,74869</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36768159$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mikra, Chrysoula</creatorcontrib><creatorcontrib>Mitrakas, Achilleas</creatorcontrib><creatorcontrib>Ghizzani, Virginia</creatorcontrib><creatorcontrib>Katsani, Katerina R</creatorcontrib><creatorcontrib>Koffa, Maria</creatorcontrib><creatorcontrib>Koukourakis, Michael</creatorcontrib><creatorcontrib>Psomas, George</creatorcontrib><creatorcontrib>Protti, Stefano</creatorcontrib><creatorcontrib>Fagnoni, Maurizio</creatorcontrib><creatorcontrib>Fylaktakidou, Konstantina C</creatorcontrib><title>Effect of Arylazo Sulfones on DNA: Binding, Cleavage, Photocleavage, Molecular Docking Studies and Interaction with A375 Melanoma and Non-Cancer Cells</title><title>International journal of molecular sciences</title><addtitle>Int J Mol Sci</addtitle><description>A set of arylazo sulfones, known to undergo N-S bond cleavage upon light exposure, has been synthesized, and their activity in the dark and upon irradiation towards DNA has been investigated. Their interaction with calf-thymus DNA has been examined, and the significant affinity observed (most probably due to DNA intercalation) was analyzed by means of molecular docking "in silico" calculations that pointed out polar contacts, mainly via the sulfonyl moiety. Incubation with plasmid pBluescript KS II revealed DNA cleavage that has been studied over time and concentration. UV-A irradiation considerably improved DNA damage for most of the compounds, whereas under visible light the effect was slightly lower. Moving to in vitro experiments, irradiation was found to slightly enhance the death of the cells in the majority of the compounds. Naphthylazosulfone
showed photo-disruptive effect under UV-A irradiation (IC
~13 μΜ) followed by derivatives
and
(IC
~100 μΜ). Those compounds were irradiated in the presence of two non-cancer cell lines and were found equally toxic only upon irradiation and not in the dark. The temporal and spatial control of light, therefore, might provide a chance for these novel scaffolds to be useful for the development of phototoxic pharmaceuticals.</description><subject>Cancer therapies</subject><subject>Cell death</subject><subject>Chemotherapy</subject><subject>Cleavage</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA - chemistry</subject><subject>DNA Cleavage</subject><subject>DNA damage</subject><subject>Experiments</subject><subject>Fluorides</subject><subject>Humans</subject><subject>Light</subject><subject>Light effects</subject><subject>Melanoma</subject><subject>Molecular docking</subject><subject>Molecular Docking Simulation</subject><subject>Nitrogen</subject><subject>Photodynamic therapy</subject><subject>Radiation damage</subject><subject>Sulfones</subject><subject>Sulfones - pharmacology</subject><subject>Thymus gland</subject><subject>Tumor cell lines</subject><subject>Ultraviolet Rays</subject><subject>Viscosity</subject><issn>1422-0067</issn><issn>1661-6596</issn><issn>1422-0067</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNpdkU9vFCEYxifGxtbWm2dD4sXDTuXPADMemqzTqk36x6R6Jiwwu6wMVGDatB_Ezyu1dbN64oX3l1948lTVawQPCenge7seE24gQS1pnlV7qMG4hpDx51vzbvUypTWEmGDavah2CeOsRbTbq36dDINRGYQBzOOdk_cBXE1uCN4kEDw4vph_AB-t19YvZ6B3Rt7IpZmBr6uQg9pcz4MzanIyguOgfhQWXOVJ2-KQXoNTn02UKtsivLV5BeaEU3BunPRhlH-Qi-DrXnplIuiNc-mg2hmkS-bV07lfff908q3_Up9dfj7t52e1ahDONYcEMyo1gw3DmDLKhhJSS0SgXiwaYrQaMOKqPEFOoKElK0S6xVDrATJN9qujR-_1tBgLbXyO0onraEcZ70SQVvy78XYlluFGdB2iHDVF8O5JEMPPyaQsRptUiSC9CVMSmHPKEG9bWtC3_6HrMEVf4j1QTYcx5m2hZo-UiiGlaIbNZxAUD4WL7cIL_mY7wAb-2zD5DZnApwE</recordid><startdate>20230117</startdate><enddate>20230117</enddate><creator>Mikra, Chrysoula</creator><creator>Mitrakas, Achilleas</creator><creator>Ghizzani, Virginia</creator><creator>Katsani, Katerina R</creator><creator>Koffa, Maria</creator><creator>Koukourakis, Michael</creator><creator>Psomas, George</creator><creator>Protti, Stefano</creator><creator>Fagnoni, Maurizio</creator><creator>Fylaktakidou, Konstantina C</creator><general>MDPI AG</general><general>MDPI</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>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-5879-7265</orcidid><orcidid>https://orcid.org/0000-0003-0247-7585</orcidid><orcidid>https://orcid.org/0000-0002-9980-7773</orcidid><orcidid>https://orcid.org/0000-0002-2186-2617</orcidid><orcidid>https://orcid.org/0000-0002-5313-5692</orcidid></search><sort><creationdate>20230117</creationdate><title>Effect of Arylazo Sulfones on DNA: Binding, Cleavage, Photocleavage, Molecular Docking Studies and Interaction with A375 Melanoma and Non-Cancer Cells</title><author>Mikra, Chrysoula ; Mitrakas, Achilleas ; Ghizzani, Virginia ; Katsani, Katerina R ; Koffa, Maria ; Koukourakis, Michael ; Psomas, George ; Protti, Stefano ; Fagnoni, Maurizio ; Fylaktakidou, Konstantina C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c412t-703265ad6046225656f002da130dbb43edcf217c2da0730e5fec01d820ddf06d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Cancer therapies</topic><topic>Cell death</topic><topic>Chemotherapy</topic><topic>Cleavage</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>DNA - chemistry</topic><topic>DNA Cleavage</topic><topic>DNA damage</topic><topic>Experiments</topic><topic>Fluorides</topic><topic>Humans</topic><topic>Light</topic><topic>Light effects</topic><topic>Melanoma</topic><topic>Molecular docking</topic><topic>Molecular Docking Simulation</topic><topic>Nitrogen</topic><topic>Photodynamic therapy</topic><topic>Radiation damage</topic><topic>Sulfones</topic><topic>Sulfones - pharmacology</topic><topic>Thymus gland</topic><topic>Tumor cell lines</topic><topic>Ultraviolet Rays</topic><topic>Viscosity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mikra, Chrysoula</creatorcontrib><creatorcontrib>Mitrakas, Achilleas</creatorcontrib><creatorcontrib>Ghizzani, Virginia</creatorcontrib><creatorcontrib>Katsani, Katerina R</creatorcontrib><creatorcontrib>Koffa, Maria</creatorcontrib><creatorcontrib>Koukourakis, Michael</creatorcontrib><creatorcontrib>Psomas, George</creatorcontrib><creatorcontrib>Protti, Stefano</creatorcontrib><creatorcontrib>Fagnoni, Maurizio</creatorcontrib><creatorcontrib>Fylaktakidou, Konstantina C</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>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest research library</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content 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 China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>International journal of molecular sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mikra, Chrysoula</au><au>Mitrakas, Achilleas</au><au>Ghizzani, Virginia</au><au>Katsani, Katerina R</au><au>Koffa, Maria</au><au>Koukourakis, Michael</au><au>Psomas, George</au><au>Protti, Stefano</au><au>Fagnoni, Maurizio</au><au>Fylaktakidou, Konstantina C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of Arylazo Sulfones on DNA: Binding, Cleavage, Photocleavage, Molecular Docking Studies and Interaction with A375 Melanoma and Non-Cancer Cells</atitle><jtitle>International journal of molecular sciences</jtitle><addtitle>Int J Mol Sci</addtitle><date>2023-01-17</date><risdate>2023</risdate><volume>24</volume><issue>3</issue><spage>1834</spage><pages>1834-</pages><issn>1422-0067</issn><issn>1661-6596</issn><eissn>1422-0067</eissn><abstract>A set of arylazo sulfones, known to undergo N-S bond cleavage upon light exposure, has been synthesized, and their activity in the dark and upon irradiation towards DNA has been investigated. Their interaction with calf-thymus DNA has been examined, and the significant affinity observed (most probably due to DNA intercalation) was analyzed by means of molecular docking "in silico" calculations that pointed out polar contacts, mainly via the sulfonyl moiety. Incubation with plasmid pBluescript KS II revealed DNA cleavage that has been studied over time and concentration. UV-A irradiation considerably improved DNA damage for most of the compounds, whereas under visible light the effect was slightly lower. Moving to in vitro experiments, irradiation was found to slightly enhance the death of the cells in the majority of the compounds. Naphthylazosulfone
showed photo-disruptive effect under UV-A irradiation (IC
~13 μΜ) followed by derivatives
and
(IC
~100 μΜ). Those compounds were irradiated in the presence of two non-cancer cell lines and were found equally toxic only upon irradiation and not in the dark. The temporal and spatial control of light, therefore, might provide a chance for these novel scaffolds to be useful for the development of phototoxic pharmaceuticals.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>36768159</pmid><doi>10.3390/ijms24031834</doi><orcidid>https://orcid.org/0000-0002-5879-7265</orcidid><orcidid>https://orcid.org/0000-0003-0247-7585</orcidid><orcidid>https://orcid.org/0000-0002-9980-7773</orcidid><orcidid>https://orcid.org/0000-0002-2186-2617</orcidid><orcidid>https://orcid.org/0000-0002-5313-5692</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Cancer therapies Cell death Chemotherapy Cleavage Deoxyribonucleic acid DNA DNA - chemistry DNA Cleavage DNA damage Experiments Fluorides Humans Light Light effects Melanoma Molecular docking Molecular Docking Simulation Nitrogen Photodynamic therapy Radiation damage Sulfones Sulfones - pharmacology Thymus gland Tumor cell lines Ultraviolet Rays Viscosity |
title | Effect of Arylazo Sulfones on DNA: Binding, Cleavage, Photocleavage, Molecular Docking Studies and Interaction with A375 Melanoma and Non-Cancer Cells |
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