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Telomere Gene Therapy: Polarizing Therapeutic Goals for Treatment of Various Diseases

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dc.contributor.authorHong, JinWoo-
dc.contributor.authorYun, Chae-Ok-
dc.date.accessioned2021-07-30T05:23:08Z-
dc.date.available2021-07-30T05:23:08Z-
dc.date.created2021-05-12-
dc.date.issued2019-05-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/4582-
dc.description.abstractModulation of telomerase maintenance by gene therapy must meet two polarizing requirements to achieve different therapeutic outcomes: Anti-aging/regenerative applications require upregulation, while anticancer applications necessitate suppression of various genes integral to telomere maintenance (e.g., telomerase, telomerase RNA components, and shelterin complex). Patients suffering from aging-associated illnesses often exhibit telomere attrition, which promotes chromosomal instability and cellular senescence, thus requiring the transfer of telomere maintenance-related genes to improve patient outcomes. However, reactivation and overexpression of telomerase are observed in 85% of cancer patients; this process is integral to cancer immortality. Thus, telomere-associated genes in the scope of cancer gene therapy must be inactivated or inhibited to induce anticancer effects. These contradicting requirements for achieving different therapeutic outcomes mean that any vector-mediated upregulation of telomere-associated genes must be accompanied by rigorous evaluation of potential oncogenesis. Thus, this review aims to discuss how telomere-associated genes are being targeted or utilized in various gene therapy applications and provides some insight into currently available safety hazard assessments.-
dc.language영어-
dc.language.isoen-
dc.publisherMDPI-
dc.titleTelomere Gene Therapy: Polarizing Therapeutic Goals for Treatment of Various Diseases-
dc.typeArticle-
dc.contributor.affiliatedAuthorYun, Chae-Ok-
dc.identifier.doi10.3390/cells8050392-
dc.identifier.wosid000470994400012-
dc.identifier.bibliographicCitationCELLS, v.8, no.5, pp.1 - 17-
dc.relation.isPartOfCELLS-
dc.citation.titleCELLS-
dc.citation.volume8-
dc.citation.number5-
dc.citation.startPage1-
dc.citation.endPage17-
dc.type.rimsART-
dc.type.docTypeReview-
dc.description.journalClass1-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.relation.journalResearchAreaCell Biology-
dc.relation.journalWebOfScienceCategoryCell Biology-
dc.subject.keywordPlusREVERSE-TRANSCRIPTASE PROMOTER-
dc.subject.keywordPlusNUCLEUS PULPOSUS CELLS-
dc.subject.keywordPlusHUMAN CANCER-CELLS-
dc.subject.keywordPlusCARDIOVASCULAR-DISEASE-
dc.subject.keywordPlusONCOLYTIC ADENOVIRUS-
dc.subject.keywordPlusMEDIATED INHIBITION-
dc.subject.keywordPlusPULMONARY-FIBROSIS-
dc.subject.keywordPlusRNA INTERFERENCE-
dc.subject.keywordPlusLIVER-CIRRHOSIS-
dc.subject.keywordPlusHTERT PROMOTER-
dc.subject.keywordAuthortelomere-
dc.subject.keywordAuthortelomerase-
dc.subject.keywordAuthortelomere dysfunction-
dc.subject.keywordAuthorgene therapy-
dc.subject.keywordAuthoranti-aging-
dc.subject.keywordAuthorregenerative medicine-
dc.subject.keywordAuthorcancer therapy-
dc.identifier.urlhttps://www.mdpi.com/2073-4409/8/5/392-
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