作者: Monika Chauhan , Gourav Sharma , Gaurav Joshi , Raj Kumar
DOI: 10.2174/1381612822666160224142200
关键词: Blot 、 Cancer 、 In vivo 、 Signal transduction 、 Epidermal growth factor receptor 、 Biology 、 Topoisomerase 、 Pharmacology 、 Electrophoretic mobility shift assay 、 Chromogenic in situ hybridization
摘要: Background: The interactions of Epidermal Growth Factor Receptor (EGFR) and topoisomerases have been seen in various cancer including brain, breast, ovarian, colorectal, gastric, etc. Methods: studies adenocarcinoma patients, chromogenic situ hybridization, western blotting, receptor binding assay electromobility shift assays, threw light on the biophysical biochemical features EGFR Topoisomerase cross-talks. Results: It has been revealed that both isomers topoisomerase (Topo I Topo II) interact via different mechanisms with EGFR. II HER2 share same location i.e. 17q12–21 regions which could be a possible cause predominant between them. are mechanically related to nucleolar translocation heparenase by EGF c-Jun. Conclusion: We compiled literature findings mechanistic interventions, signaling pathways, patents, vitro vivo data tested inhibitors and combinations clinical trials, provide convincing confirmations for topoisomerases. These may be used deriving consistent route mechanism, design development standard drug and dual or multi inhibitors.