EGFR is a potential dual molecular target for cancer and Alzheimer’s disease
DC Field | Value | Language |
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dc.contributor.author | Choi, Hee-Jeong | - |
dc.contributor.author | Jeong, Yoo Joo | - |
dc.contributor.author | Kim, Jieun | - |
dc.contributor.author | Hoe, Hyang-Sook | - |
dc.date.accessioned | 2023-09-19T04:23:53Z | - |
dc.date.available | 2023-09-19T04:23:53Z | - |
dc.date.created | 2023-09-05 | - |
dc.date.issued | 2023-08 | - |
dc.identifier.issn | 1663-9812 | - |
dc.identifier.uri | http://scholarworks.bwise.kr/kbri/handle/2023.sw.kbri/972 | - |
dc.description.abstract | Many researchers are attempting to identify drugs that can be repurposed as effective therapies for Alzheimer's disease (AD). Several recent studies have highlighted epidermal growth factor receptor (EGFR) inhibitors approved for use as anti-cancer drugs as potential candidates for repurposing as AD therapeutics. In cancer, EGFR inhibitors target cell proliferation and angiogenesis, and studies in AD mouse models have shown that EGFR inhibitors can attenuate amyloid-beta (A beta) pathology and improve cognitive function. In this review, we discuss the different functions of EGFR in cancer and AD and the potential of EGFR as a dual molecular target for AD diseases. In addition, we describe the effects of anti-cancer EGFR tyrosine kinase inhibitors (TKIs) on AD pathology and their prospects as therapeutic interventions for AD. By summarizing the physiological functions of EGFR in cancer and AD, this review emphasizes the significance of EGFR as an important molecular target for these diseases. | - |
dc.publisher | Frontiers Media SA | - |
dc.title | EGFR is a potential dual molecular target for cancer and Alzheimer’s disease | - |
dc.type | Article | - |
dc.contributor.affiliatedAuthor | Hoe, Hyang-Sook | - |
dc.identifier.doi | 10.3389/fphar.2023.1238639 | - |
dc.identifier.scopusid | 2-s2.0-85168280164 | - |
dc.identifier.wosid | 001049960900001 | - |
dc.identifier.bibliographicCitation | Frontiers in Pharmacology, v.14 | - |
dc.relation.isPartOf | Frontiers in Pharmacology | - |
dc.citation.title | Frontiers in Pharmacology | - |
dc.citation.volume | 14 | - |
dc.type.rims | ART | - |
dc.type.docType | Review | - |
dc.description.journalClass | 1 | - |
dc.description.isOpenAccess | Y | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Pharmacology & Pharmacy | - |
dc.relation.journalWebOfScienceCategory | Pharmacology & Pharmacy | - |
dc.subject.keywordPlus | EPIDERMAL-GROWTH-FACTOR | - |
dc.subject.keywordPlus | CELL LUNG-CANCER | - |
dc.subject.keywordPlus | FACTOR-RECEPTOR | - |
dc.subject.keywordPlus | TYROSINE KINASE | - |
dc.subject.keywordPlus | DOWN-REGULATION | - |
dc.subject.keywordPlus | POOR-PROGNOSIS | - |
dc.subject.keywordPlus | ERLOTINIB | - |
dc.subject.keywordPlus | EXPRESSION | - |
dc.subject.keywordPlus | RESISTANCE | - |
dc.subject.keywordPlus | INHIBITION | - |
dc.subject.keywordAuthor | Alzheimer&apos | - |
dc.subject.keywordAuthor | s disease | - |
dc.subject.keywordAuthor | EGFR | - |
dc.subject.keywordAuthor | EGFR inhibitor | - |
dc.subject.keywordAuthor | cancer | - |
dc.subject.keywordAuthor | A beta | - |
dc.subject.keywordAuthor | learning and memory | - |
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