Recent updates on the therapeutic potential of HER2 tyrosine kinase inhibitors for the treatment of breast cancer

dc.contributor.authorSingla, Heena
dc.contributor.authorMunshi, Anjana
dc.contributor.authorBanipal, Raja Paramjit Singh
dc.contributor.authorKumar, Vinod
dc.date.accessioned2018-07-14T01:19:06Z
dc.date.accessioned2024-08-14T07:41:22Z
dc.date.available2018-07-14T01:19:06Z
dc.date.available2024-08-14T07:41:22Z
dc.date.issued2018
dc.description.abstractHER2 positive breast cancer is characterized by the low survival rate in the metastatic patients. Development of resistance and disease-relapse are the major problems associated with the currently available therapies for HER2 positive breast cancer. There are two major targeted therapies for HER2 positive breast cancer viz. monoclonal antibodies and tyrosine-kinase inhibitors, and both of these therapies have their advantages and limitations. To address the limitations associated with the existing therapies, use of antibodies and TKIs as combination therapy proved to be more effective. Various chemical modifications can be performed on tyrosine-kinase inhibitors to develop novel ligands with increased selectivity for HER2 kinase. A number of tyrosine-kinase inhibitors are in various phases of clinical trials for the treatment of HER2 positive breast cancer. In the current review article, recent developments on various HER2 tyrosine-kinase inhibitors have been reported. Various structurally different scaffolds bind to the HER2 receptor and exhibit potent anti-cancer activities. The structural and pharmacophoric requirements of the scaffolds are discussed in detail so as to discover effective drug candidates for the treatment of HER2 positive breast cancer. ? 2018 Bentham Science Publishers.en_US
dc.identifier.citationSingla, H., Munshi, A., Banipal, R. P. S., & Kumar, V. (2018). Recent updates on the therapeutic potential of HER2 tyrosine kinase inhibitors for the treatment of breast cancer. Current Cancer Drug Targets, 18(4), 306-327. doi: 10.2174/1568009617666170623122213en_US
dc.identifier.doi10.2174/1568009617666170623122213
dc.identifier.issn15680096
dc.identifier.urihttps://kr.cup.edu.in/handle/32116/1446
dc.identifier.urlhttp://www.eurekaselect.com/153604/article
dc.language.isoen_USen_US
dc.publisherBentham Science Publishers B.V.en_US
dc.subject4 [1 (3 fluorobenzyl) 5 indazolylamino] 5 methylpyrrolo[2,1 f][1,2,4]triazine 6 carbamic acid 3 morpholinomethyl esteren_US
dc.subject6 [4 (4 ethyl 1 piperazinylmethyl)phenyl] 4 (alpha methylbenzylamino) 7h pyrrolo[2,3 d]pyrimidineen_US
dc.subjectafatiniben_US
dc.subjectbms 690514en_US
dc.subjectcanertiniben_US
dc.subjectcp 724714en_US
dc.subjectcudc 101en_US
dc.subjectdacomitiniben_US
dc.subjectepertiniben_US
dc.subjectepidermal growth factor receptoren_US
dc.subjectepidermal growth factor receptor 2en_US
dc.subjectepidermal growth factor receptor kinase inhibitoren_US
dc.subjectkbp 5209en_US
dc.subjectlapatiniben_US
dc.subjectmubritiniben_US
dc.subjectn [4 [3 chloro 4 (3 fluorobenzyloxy)anilino] 6 qen_US
dc.titleRecent updates on the therapeutic potential of HER2 tyrosine kinase inhibitors for the treatment of breast canceren_US
dc.title.journalCurrent Cancer Drug Targets
dc.typeReviewen_US

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