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Non-cancer to anti-cancer: investigation of human ether-a-go-go-related gene potassium channel inhibitors as potential therapeutics
Background The expression of hERG K.sup.+ channels is observed in various cancer cells including epithelial, neuronal, leukemic, and connective tissue. The role of hERG potassium channels in regulating the growth and death of cancer cells include cell proliferation, survival, secretion of proangioge...
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Published in: | Journal of Egyptian National Cancer Institute 2021-11, Vol.33 (1), p.1-16 |
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description | Background The expression of hERG K.sup.+ channels is observed in various cancer cells including epithelial, neuronal, leukemic, and connective tissue. The role of hERG potassium channels in regulating the growth and death of cancer cells include cell proliferation, survival, secretion of proangiogenic factors, invasiveness, and metastasis. Methods In the reported study, an attempt has been made to investigate some non-cancer hERG blockers as potential cancer therapeutics using a computational drug repurposing strategy. Preliminary investigation for hERG blockers/non-blockers has identified 26 potential clinically approved compounds for further studies using molecular modeling. Results The interactions at the binding pockets have been investigated along with the prioritization based on the binding score. Some of the identified potential hERG inhibitors, i.e., Bromocriptine, Darglitazone, and Troglitazone, have been investigated to derive the mechanism of cancer inhibition. Conclusions The proposed mechanism for anti-cancer properties via hERG blocking for some of the potential compounds is required to be explored using other experimental methodologies. The drug repurposing approach applied to investigate anti-cancer therapeutics may direct to provide a therapeutic solution to late-stage cancer and benefit a significant population of patients. |
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The role of hERG potassium channels in regulating the growth and death of cancer cells include cell proliferation, survival, secretion of proangiogenic factors, invasiveness, and metastasis. Methods In the reported study, an attempt has been made to investigate some non-cancer hERG blockers as potential cancer therapeutics using a computational drug repurposing strategy. Preliminary investigation for hERG blockers/non-blockers has identified 26 potential clinically approved compounds for further studies using molecular modeling. Results The interactions at the binding pockets have been investigated along with the prioritization based on the binding score. Some of the identified potential hERG inhibitors, i.e., Bromocriptine, Darglitazone, and Troglitazone, have been investigated to derive the mechanism of cancer inhibition. Conclusions The proposed mechanism for anti-cancer properties via hERG blocking for some of the potential compounds is required to be explored using other experimental methodologies. The drug repurposing approach applied to investigate anti-cancer therapeutics may direct to provide a therapeutic solution to late-stage cancer and benefit a significant population of patients.</description><identifier>ISSN: 1110-0362</identifier><identifier>EISSN: 2589-0409</identifier><identifier>DOI: 10.1186/s43046-021-00091-3</identifier><language>eng</language><publisher>Cairo: Springer</publisher><subject>Anti-cancer agents ; Apoptosis ; Cancer ; Cardiac arrhythmia ; Cardiotoxicity ; Care and treatment ; Cell cycle ; Cell growth ; Datasets ; Diabetes ; Dofetilide ; Drug repurposing ; Drug therapy ; FDA approval ; Genetic aspects ; Genetic research ; hERG inhibitors ; Hypoglycemic agents ; Investigations ; Leukemia ; Molecular docking ; Non-cancer ; Oncology, Experimental ; Potassium ; Potassium channels ; Prevention ; Thioridazine</subject><ispartof>Journal of Egyptian National Cancer Institute, 2021-11, Vol.33 (1), p.1-16</ispartof><rights>COPYRIGHT 2021 Springer</rights><rights>The Author(s) 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c529t-df93b7fe542479aa259623088d1aacce530e9987a3f3edea6325bdfcef71c6d73</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2729536144/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2729536144?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,25753,27924,27925,37012,44590,75126</link.rule.ids></links><search><creatorcontrib>Patil, Vaishali M</creatorcontrib><creatorcontrib>Gaurav, Anand</creatorcontrib><creatorcontrib>Garg, Priyanka</creatorcontrib><creatorcontrib>Masand, Neeraj</creatorcontrib><title>Non-cancer to anti-cancer: investigation of human ether-a-go-go-related gene potassium channel inhibitors as potential therapeutics</title><title>Journal of Egyptian National Cancer Institute</title><description>Background The expression of hERG K.sup.+ channels is observed in various cancer cells including epithelial, neuronal, leukemic, and connective tissue. The role of hERG potassium channels in regulating the growth and death of cancer cells include cell proliferation, survival, secretion of proangiogenic factors, invasiveness, and metastasis. Methods In the reported study, an attempt has been made to investigate some non-cancer hERG blockers as potential cancer therapeutics using a computational drug repurposing strategy. Preliminary investigation for hERG blockers/non-blockers has identified 26 potential clinically approved compounds for further studies using molecular modeling. Results The interactions at the binding pockets have been investigated along with the prioritization based on the binding score. Some of the identified potential hERG inhibitors, i.e., Bromocriptine, Darglitazone, and Troglitazone, have been investigated to derive the mechanism of cancer inhibition. Conclusions The proposed mechanism for anti-cancer properties via hERG blocking for some of the potential compounds is required to be explored using other experimental methodologies. The drug repurposing approach applied to investigate anti-cancer therapeutics may direct to provide a therapeutic solution to late-stage cancer and benefit a significant population of patients.</description><subject>Anti-cancer agents</subject><subject>Apoptosis</subject><subject>Cancer</subject><subject>Cardiac arrhythmia</subject><subject>Cardiotoxicity</subject><subject>Care and treatment</subject><subject>Cell cycle</subject><subject>Cell growth</subject><subject>Datasets</subject><subject>Diabetes</subject><subject>Dofetilide</subject><subject>Drug repurposing</subject><subject>Drug therapy</subject><subject>FDA approval</subject><subject>Genetic aspects</subject><subject>Genetic research</subject><subject>hERG inhibitors</subject><subject>Hypoglycemic agents</subject><subject>Investigations</subject><subject>Leukemia</subject><subject>Molecular docking</subject><subject>Non-cancer</subject><subject>Oncology, Experimental</subject><subject>Potassium</subject><subject>Potassium channels</subject><subject>Prevention</subject><subject>Thioridazine</subject><issn>1110-0362</issn><issn>2589-0409</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkM-LFTEMxwdR8Ln6D3gqeO7a3zP1tiz-WFj0ouch00nn9THTPtuO4Nl_3D53QQ-SQEjyzSchXfeas2vOB_O2KMmUoUxwyhiznMon3UHowVKmmH3aHTjnjDJpxPPuRSknxoxhvT50vz6nSB1Eh5nURCDW8Ji-IyH-wFLDAjWkSJInx32DSLAeMVOgS7p4xhUqzmTBiOScKpQS9o24I8SIa2McwxRqyoVAufSxbYCVXBhwxr0GV152zzysBV89xqvu24f3X28_0fsvH-9ub-6p08JWOnsrp96jVkL1FkBoa4RkwzBzAOdQS4bWDj1IL3FGMFLoafYOfc-dmXt51d09cOcEp_Gcwwb555ggjH8KKS8j5HbQiiNzSs-9V4ZNTCnFQbZEajV5Z3WvZWO9eWCdc_q-tzeNp7Tn2M4fRS-sloYr9Ve1QIOG6FPN4LZQ3HhjBq6t7QfdVNf_UTWbcQsuRfSh1f8Z-A0L6Jlj</recordid><startdate>20211108</startdate><enddate>20211108</enddate><creator>Patil, Vaishali M</creator><creator>Gaurav, Anand</creator><creator>Garg, Priyanka</creator><creator>Masand, Neeraj</creator><general>Springer</general><general>Springer Nature B.V</general><general>SpringerOpen</general><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</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>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>NAPCQ</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>DOA</scope></search><sort><creationdate>20211108</creationdate><title>Non-cancer to anti-cancer: investigation of human ether-a-go-go-related gene potassium channel inhibitors as potential therapeutics</title><author>Patil, Vaishali M ; Gaurav, Anand ; Garg, Priyanka ; Masand, Neeraj</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c529t-df93b7fe542479aa259623088d1aacce530e9987a3f3edea6325bdfcef71c6d73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Anti-cancer agents</topic><topic>Apoptosis</topic><topic>Cancer</topic><topic>Cardiac arrhythmia</topic><topic>Cardiotoxicity</topic><topic>Care and treatment</topic><topic>Cell cycle</topic><topic>Cell growth</topic><topic>Datasets</topic><topic>Diabetes</topic><topic>Dofetilide</topic><topic>Drug repurposing</topic><topic>Drug therapy</topic><topic>FDA approval</topic><topic>Genetic aspects</topic><topic>Genetic research</topic><topic>hERG inhibitors</topic><topic>Hypoglycemic agents</topic><topic>Investigations</topic><topic>Leukemia</topic><topic>Molecular docking</topic><topic>Non-cancer</topic><topic>Oncology, Experimental</topic><topic>Potassium</topic><topic>Potassium channels</topic><topic>Prevention</topic><topic>Thioridazine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Patil, Vaishali M</creatorcontrib><creatorcontrib>Gaurav, Anand</creatorcontrib><creatorcontrib>Garg, Priyanka</creatorcontrib><creatorcontrib>Masand, Neeraj</creatorcontrib><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</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 Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Nursing & Allied Health Premium</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>DOAJ Directory of Open Access Journals</collection><jtitle>Journal of Egyptian National Cancer Institute</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Patil, Vaishali M</au><au>Gaurav, Anand</au><au>Garg, Priyanka</au><au>Masand, Neeraj</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Non-cancer to anti-cancer: investigation of human ether-a-go-go-related gene potassium channel inhibitors as potential therapeutics</atitle><jtitle>Journal of Egyptian National Cancer Institute</jtitle><date>2021-11-08</date><risdate>2021</risdate><volume>33</volume><issue>1</issue><spage>1</spage><epage>16</epage><pages>1-16</pages><issn>1110-0362</issn><eissn>2589-0409</eissn><abstract>Background The expression of hERG K.sup.+ channels is observed in various cancer cells including epithelial, neuronal, leukemic, and connective tissue. The role of hERG potassium channels in regulating the growth and death of cancer cells include cell proliferation, survival, secretion of proangiogenic factors, invasiveness, and metastasis. Methods In the reported study, an attempt has been made to investigate some non-cancer hERG blockers as potential cancer therapeutics using a computational drug repurposing strategy. Preliminary investigation for hERG blockers/non-blockers has identified 26 potential clinically approved compounds for further studies using molecular modeling. Results The interactions at the binding pockets have been investigated along with the prioritization based on the binding score. Some of the identified potential hERG inhibitors, i.e., Bromocriptine, Darglitazone, and Troglitazone, have been investigated to derive the mechanism of cancer inhibition. Conclusions The proposed mechanism for anti-cancer properties via hERG blocking for some of the potential compounds is required to be explored using other experimental methodologies. The drug repurposing approach applied to investigate anti-cancer therapeutics may direct to provide a therapeutic solution to late-stage cancer and benefit a significant population of patients.</abstract><cop>Cairo</cop><pub>Springer</pub><doi>10.1186/s43046-021-00091-3</doi><tpages>16</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Anti-cancer agents Apoptosis Cancer Cardiac arrhythmia Cardiotoxicity Care and treatment Cell cycle Cell growth Datasets Diabetes Dofetilide Drug repurposing Drug therapy FDA approval Genetic aspects Genetic research hERG inhibitors Hypoglycemic agents Investigations Leukemia Molecular docking Non-cancer Oncology, Experimental Potassium Potassium channels Prevention Thioridazine |
title | Non-cancer to anti-cancer: investigation of human ether-a-go-go-related gene potassium channel inhibitors as potential therapeutics |
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