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Cited 24 time in webofscience Cited 27 time in scopus
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Targeting autophagy in gastrointestinal malignancy by using nanomaterials as drug delivery systems

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dc.contributor.authorRaju, G. Seeta Rama-
dc.contributor.authorPavitra, E.-
dc.contributor.authorMerchant, Neha-
dc.contributor.authorLee, Hoomin-
dc.contributor.authorPrasad, Ganji Lakshmi Vara-
dc.contributor.authorNagaraju, Ganji Purnachandra-
dc.contributor.authorHuh, Yun Suk-
dc.contributor.authorHan, Young-Kyu-
dc.date.accessioned2024-09-26T13:31:49Z-
dc.date.available2024-09-26T13:31:49Z-
dc.date.issued2018-04-10-
dc.identifier.issn0304-3835-
dc.identifier.issn1872-7980-
dc.identifier.urihttps://scholarworks.dongguk.edu/handle/sw.dongguk/25259-
dc.description.abstractAutophagy is a conserved catabolic process involving large protein degradation by a ubiquitous auto-phagosomic signaling pathway, which is essential for cellular homeostasis. It is triggered by environmental factors such as stress, lack of nutrients, inflammation, and eliminating intracellular pathogens. Although the mechanisms underlying autophagy are still unclear, increasing evidence illuminates the magnitude of autophagy in a wide range of physiological processes and human diseases. Simultaneously, research community has focused on the triggering of autophagy by the internalization of engineered nanomaterials, which indicates a new line of revolution in cancer cure. However, most studies on nanoparticle-induced autophagy focus on brain, breast, and cervical cancers; limited reports are available on gastrointestinal (GI) cancers. Therefore, the aim of this mini review is to discuss in detail the role of autophagy in GI malignancy and the status of research on nanoparticle-induced autophagy. (C) 2018 Elsevier B.V. All rights reserved.-
dc.format.extent11-
dc.language영어-
dc.language.isoENG-
dc.publisherELSEVIER IRELAND LTD-
dc.titleTargeting autophagy in gastrointestinal malignancy by using nanomaterials as drug delivery systems-
dc.typeArticle-
dc.publisher.location아일랜드-
dc.identifier.doi10.1016/j.canlet.2018.01.044-
dc.identifier.scopusid2-s2.0-85041381574-
dc.identifier.wosid000427102300022-
dc.identifier.bibliographicCitationCANCER LETTERS, v.419, pp 222 - 232-
dc.citation.titleCANCER LETTERS-
dc.citation.volume419-
dc.citation.startPage222-
dc.citation.endPage232-
dc.type.docTypeReview-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaOncology-
dc.relation.journalWebOfScienceCategoryOncology-
dc.subject.keywordPlusHEPATOCELLULAR-CARCINOMA CELLS-
dc.subject.keywordPlusHYPOXIA-INDUCED AUTOPHAGY-
dc.subject.keywordPlusESOPHAGEAL CANCER-CELLS-
dc.subject.keywordPlusCOLON-CANCER-
dc.subject.keywordPlusSIGNALING PATHWAYS-
dc.subject.keywordPlusVACUOLATING CYTOTOXIN-
dc.subject.keywordPlusESOPHAGOGASTRIC CANCER-
dc.subject.keywordPlusOXIDE NANOPARTICLES-
dc.subject.keywordPlusGROWTH-INHIBITION-
dc.subject.keywordPlusINDUCE AUTOPHAGY-
dc.subject.keywordAuthorAutophagy-
dc.subject.keywordAuthorNanomaterial-
dc.subject.keywordAuthorGastric cancer-
dc.subject.keywordAuthorPancreatic cancer-
dc.subject.keywordAuthorLiver cancer-
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