Epidermal Growth Factor Receptor (EGFR) and its Cross-Talks with Topoisomerases: Challenges and Opportunities for Multi-Target Anticancer Drugs

dc.contributor.authorChauhan, Monika
dc.contributor.authorSharma, Gourav
dc.contributor.authorJoshi, Gaurav
dc.contributor.authorKumar, Raj
dc.date.accessioned2017-08-03T09:02:44Z
dc.date.accessioned2024-08-13T12:05:42Z
dc.date.available2017-08-03T09:02:44Z
dc.date.available2024-08-13T12:05:42Z
dc.date.issued2016
dc.description.abstractBackground: The interactions of Epidermal Growth Factor Receptor (EGFR) and topoisomerases have been seen in various cancer including brain, breast, ovarian, colorectal, gastric, etc. Methods: The studies in adenocarcinoma patients, chromogenic in situ hybridization, western blotting, receptor binding assay and electromobility shift assays, etc. threw light on the biophysical and biochemical features of EGFR and Topoisomerase cross-talks. Results: It has been revealed that both the isomers of topoisomerase (Topo I and Topo II) interact via different mechanisms with EGFR. Topo II and HER2 share the same location i.e. 17q12-21 regions which could be a possible cause of predominant interactions seen between them. Topo I and EGFR interactions are mechanically related to the nucleolar translocation of heparenase by EGF and c-Jun. Conclusion: We compiled literature findings including the mechanistic interventions, signaling pathways, patents, in vitro and in vivo data of tested inhibitors and combinations in clinical trials, which provide convincing confirmations for the interactions of EGFR and topoisomerases. These interactions may be used for deriving a consistent route of mechanism, design and development of standard drug combinations and dual or multi inhibitors. ? 2016 Bentham Science Publishers.en_US
dc.identifier.citationChauhan, M., Sharma, G., Joshi, G., & Kumar, R. (2016). Epidermal Growth Factor Receptor (EGFR) and its Cross-Talks with Topoisomerases: Challenges and Opportunities for Multi-Target Anticancer Drugs. Current Pharmaceutical Design, 22(21), 3226-3236. doi: 10.2174/1381612822666160224142200en_US
dc.identifier.doi10.2174/1381612822666160224142200
dc.identifier.issn13816128
dc.identifier.urihttps://kr.cup.edu.in/handle/32116/275
dc.identifier.urlhttp://www.eurekaselect.com/139782/article
dc.language.isoenen_US
dc.publisherBentham Science Publishers B.V.en_US
dc.subjectantineoplastic agenten_US
dc.subjectDNA topoisomeraseen_US
dc.subjectDNA topoisomerase (ATP hydrolysing)en_US
dc.subjectDNA topoisomerase inhibitoren_US
dc.subjectepidermal growth factor receptoren_US
dc.subjectepidermal growth factor receptor 2en_US
dc.subjectepidermal growth factor receptor kinase inhibitoren_US
dc.subjectheparin lyaseen_US
dc.subjectprotein c junen_US
dc.subjectantineoplastic agenten_US
dc.subjectDNA topoisomeraseen_US
dc.subjectDNA topoisomerase (ATP hydrolysing)en_US
dc.subjectepidermal growth factor receptoren_US
dc.subjectadenocarcinomaen_US
dc.subjectantineoplastic activity cancer patienten_US
dc.subjectdrug mechanismen_US
dc.subjectdrug receptor bindingen_US
dc.subjectgel mobility shift assay;en_US
dc.titleEpidermal Growth Factor Receptor (EGFR) and its Cross-Talks with Topoisomerases: Challenges and Opportunities for Multi-Target Anticancer Drugsen_US
dc.title.journalCurrent Pharmaceutical Design
dc.typeArticleen_US

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