Shiga toxins as multi-functional proteins: induction of host cellular stress responses, role in pathogenesis and therapeutic applications = 감염성 시가독소의 다중기능성: 숙주세포 반응유도, 병리기전 및 치료에의 적용

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dc.contributor.authorMoo-Seung Lee-
dc.contributor.authorS Koo-
dc.contributor.authorDae Gwin Jeong-
dc.contributor.authorV L Tesh-
dc.date.accessioned2017-04-19T10:19:02Z-
dc.date.available2017-04-19T10:19:02Z-
dc.date.issued2016-
dc.identifier.issn2072-6651-
dc.identifier.uri10.3390/toxins8030077ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/13195-
dc.description.abstractShiga toxins (Stxs) produced by Shiga toxin-producing bacteria Shigella dysenteriae serotype 1 and select serotypes of Escherichia coli are primary virulence factors in the pathogenesis of hemorrhagic colitis progressing to potentially fatal systemic complications, such as hemolytic uremic syndrome and central nervous system abnormalities. Current therapeutic options to treat patients infected with toxin-producing bacteria are limited. The structures of Stxs, toxin-receptor binding, intracellular transport and the mode of action of the toxins have been well defined. However, in the last decade, numerous studies have demonstrated that in addition to being potent protein synthesis inhibitors, Stxs are also multifunctional proteins capable of activating multiple cell stress signaling pathways, which may result in apoptosis, autophagy or activation of the innate immune response. Here, we briefly present the current understanding of Stx-activated signaling pathways and provide a concise review of therapeutic applications to target tumors by engineering the toxins.-
dc.publisherMDPI-
dc.titleShiga toxins as multi-functional proteins: induction of host cellular stress responses, role in pathogenesis and therapeutic applications = 감염성 시가독소의 다중기능성: 숙주세포 반응유도, 병리기전 및 치료에의 적용-
dc.title.alternativeShiga toxins as multi-functional proteins: induction of host cellular stress responses, role in pathogenesis and therapeutic applications-
dc.typeArticle-
dc.citation.titleToxins-
dc.citation.number3-
dc.citation.endPage77-
dc.citation.startPage77-
dc.citation.volume8-
dc.contributor.affiliatedAuthorMoo-Seung Lee-
dc.contributor.affiliatedAuthorDae Gwin Jeong-
dc.contributor.alternativeName이무승-
dc.contributor.alternativeName구선우-
dc.contributor.alternativeName정대균-
dc.contributor.alternativeNameTesh-
dc.identifier.bibliographicCitationToxins, vol. 8, no. 3, pp. 77-77-
dc.identifier.doi10.3390/toxins8030077-
dc.subject.keywordShiga toxins-
dc.subject.keywordShiga toxin type 1 and 2-
dc.subject.keywordShiga toxin-producing Escherichia coli-
dc.subject.keywordhemolytic uremic syndrome-
dc.subject.keywordsignaling pathways-
dc.subject.keywordcancer therapeutics-
dc.subject.localShiga Toxin-
dc.subject.localShiga toxin-
dc.subject.localShiga toxins-
dc.subject.localShiga toxin types 1 and 2-
dc.subject.localShiga toxin type 1 and 2-
dc.subject.localShiga-toxin-producing Escherichia coli (STEC)-
dc.subject.localShiga toxin-producing Escherichia coli-
dc.subject.localHemolytic uremic syndrome-
dc.subject.localHemolytic uremic syndrome (HUS)-
dc.subject.localHemolytic Uremic Syndrome-
dc.subject.localhemolytic uremic syndrome-
dc.subject.localhemolytic uremic syndrome-
dc.subject.localHemolytic Uremic Syndrome (HUS)-
dc.subject.localSignaling pathways-
dc.subject.localsignaling pathways-
dc.subject.localSignaling pathway-
dc.subject.localcancer therapeutics-
dc.description.journalClassY-
Appears in Collections:
Division of Research on National Challenges > Environmental diseases research center > 1. Journal Articles
Division of Research on National Challenges > Bionanotechnology Research Center > 1. Journal Articles
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