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dc.contributor.author Kim, Eun-Kyoung -
dc.contributor.author Yu, Seong-Woon -
dc.contributor.author Lee, Sung Bae -
dc.date.accessioned 2021-07-15T20:07:58Z -
dc.date.available 2021-07-15T20:07:58Z -
dc.date.created 2021-07-15 -
dc.date.issued 2021-01 -
dc.identifier.citation Autophagy, v.17, no.1, pp.1 - 382 -
dc.identifier.issn 1554-8627 -
dc.identifier.uri http://hdl.handle.net/20.500.11750/13868 -
dc.description.abstract In 2008, we published the first set of guidelines for standardizing research in autophagy. Since then, this topic has received increasing attention, and many scientists have entered the field. Our knowledge base and relevant new technologies have also been expanding. Thus, it is important to formulate on a regular basis updated guidelines for monitoring autophagy in different organisms. Despite numerous reviews, there continues to be confusion regarding acceptable methods to evaluate autophagy, especially in multicellular eukaryotes. Here, we present a set of guidelines for investigators to select and interpret methods to examine autophagy and related processes, and for reviewers to provide realistic and reasonable critiques of reports that are focused on these processes. These guidelines are not meant to be a dogmatic set of rules, because the appropriateness of any assay largely depends on the question being asked and the system being used. Moreover, no individual assay is perfect for every situation, calling for the use of multiple techniques to properly monitor autophagy in each experimental setting. Finally, several core components of the autophagy machinery have been implicated in distinct autophagic processes (canonical and noncanonical autophagy), implying that genetic approaches to block autophagy should rely on targeting two or more autophagy-related genes that ideally participate in distinct steps of the pathway. Along similar lines, because multiple proteins involved in autophagy also regulate other cellular pathways including apoptosis, not all of them can be used as a specific marker for bona fide autophagic responses. Here, we critically discuss current methods of assessing autophagy and the information they can, or cannot, provide. Our ultimate goal is to encourage intellectual and technical innovation in the field. © 2020 Informa UK Limited, trading as Taylor & Francis Group. -
dc.language English -
dc.publisher Bellwether Publishing, Ltd. -
dc.title Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition) -
dc.type Article -
dc.identifier.doi 10.1080/15548627.2020.1797280 -
dc.identifier.wosid 000636121800001 -
dc.identifier.scopusid 2-s2.0-85102619204 -
dc.type.local Article(Overseas) -
dc.type.rims ART -
dc.description.journalClass 1 -
dc.citation.publicationname Autophagy -
dc.identifier.citationVolume 17 -
dc.identifier.citationNumber 1 -
dc.identifier.citationStartPage 1 -
dc.identifier.citationEndPage 382 -
dc.identifier.citationTitle Autophagy -
dc.description.isOpenAccess Y -
dc.subject.keywordAuthor Autophagosome -
dc.subject.keywordAuthor cancer -
dc.subject.keywordAuthor flux -
dc.subject.keywordAuthor LC3 -
dc.subject.keywordAuthor lysosome -
dc.subject.keywordAuthor macroautophagy -
dc.subject.keywordAuthor neurodegeneration -
dc.subject.keywordAuthor phagophore -
dc.subject.keywordAuthor stress -
dc.subject.keywordAuthor vacuole -
dc.subject.keywordPlus CHAPERONE-MEDIATED AUTOPHAGY -
dc.subject.keywordPlus ACTIVATED PROTEIN-KINASE -
dc.subject.keywordPlus PROGRAMMED CELL-DEATH -
dc.subject.keywordPlus STARVATION-INDUCED AUTOPHAGY -
dc.subject.keywordPlus ENDOPLASMIC-RETICULUM STRESS -
dc.subject.keywordPlus NF-KAPPA-B -
dc.subject.keywordPlus BREAST-CANCER CELLS -
dc.subject.keywordPlus LIFE-SPAN EXTENSION -
dc.subject.keywordPlus AMYOTROPHIC-LATERAL-SCLEROSI -
dc.subject.keywordPlus SGENOME-WIDE ASSOCIATION -
dc.contributor.affiliatedAuthor Kim, Eun-Kyoung -
dc.contributor.affiliatedAuthor Yu, Seong-Woon -
dc.contributor.affiliatedAuthor Lee, Sung Bae -

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