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Developing theragnostics for Alzheimer's disease: Insights from cancer treatment

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dc.contributor.authorLee, Hyun ju-
dc.contributor.authorHee-Jeong Choi-
dc.contributor.authorYoo Joo Jeong-
dc.contributor.authorYoon-Hee Na-
dc.contributor.authorJin Tae Hong-
dc.contributor.authorJi Min Han-
dc.contributor.authorHoe, Hyang-Sook-
dc.contributor.authorKey-Hwan Lim-
dc.date.accessioned2024-06-14T01:00:17Z-
dc.date.available2024-06-14T01:00:17Z-
dc.date.issued2024-06-
dc.identifier.issn0141-8130-
dc.identifier.issn1879-0003-
dc.identifier.urihttp://scholarworks.bwise.kr/kbri/handle/2023.sw.kbri/1182-
dc.description.abstractThe prevalence of Alzheimer's disease (AD) and its associated economic and societal burdens are on the rise, but there are no curative treatments for AD. Interestingly, this neurodegenerative disease shares several biological and pathophysiological features with cancer, including cell-cycle dysregulation, angiogenesis, mitochondrial dysfunction, protein misfolding, and DNA damage. However, the genetic factors contributing to the overlap in biological processes between cancer and AD have not been actively studied. In this review, we discuss the shared biological features of cancer and AD, the molecular targets of anticancer drugs, and therapeutic approaches. First, we outline the common biological features of cancer and AD. Second, we describe several anticancer drugs, their molecular targets, and their effects on AD pathology. Finally, we discuss how protein–protein interactions (PPIs), receptor inhibition, immunotherapy, and gene therapy can be exploited for the cure and management of both cancer and AD. Collectively, this review provides insights for the development of AD theragnostics based on cancer drugs and molecular targets.-
dc.language영어-
dc.language.isoENG-
dc.publisherElsevier BV-
dc.titleDeveloping theragnostics for Alzheimer's disease: Insights from cancer treatment-
dc.typeArticle-
dc.publisher.location네델란드-
dc.identifier.doi10.1016/j.ijbiomac.2024.131925-
dc.identifier.wosid001240388300001-
dc.identifier.bibliographicCitationInternational Journal of Biological Macromolecules, v.269-
dc.citation.titleInternational Journal of Biological Macromolecules-
dc.citation.volume269-
dc.type.docTypeReview-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaPolymer Science-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryChemistry, Applied-
dc.relation.journalWebOfScienceCategoryPolymer Science-
dc.subject.keywordPlusENDOTHELIAL GROWTH-FACTOR-
dc.subject.keywordPlusINDUCED MITOCHONDRIAL DYSFUNCTION-
dc.subject.keywordPlusHYPOXIA-INDUCIBLE FACTOR-1-
dc.subject.keywordPlusAMYLOID PRECURSOR PROTEIN-
dc.subject.keywordPlusCELL-CYCLE PROGRESSION-
dc.subject.keywordPlusBLOOD-BRAIN-BARRIER-
dc.subject.keywordPlusBREAST-CANCER-
dc.subject.keywordPlusFACTOR RECEPTOR-
dc.subject.keywordPlusMOUSE MODEL-
dc.subject.keywordPlusGENE-THERAPY-
dc.subject.keywordAuthoralzheimer 's disease-
dc.subject.keywordAuthorcancer-
dc.subject.keywordAuthorDrug discovery-
dc.subject.keywordAuthorMitochondrial dysfunction-
dc.subject.keywordAuthorAngiogenesis-
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