Hsp60 as a novel target in IBD management: A prospect

dc.contributor.authorCappello, Francesco
dc.contributor.authorMazzola, Margherita
dc.contributor.authorJurjus, Abdo R.
dc.contributor.authorZeenny, Marie Noel
dc.contributor.authorJurjus, Rosalyn A.
dc.contributor.authorCarini, Francesco
dc.contributor.authorLeone, Angelo
dc.contributor.authorBonaventura, Giuseppe
dc.contributor.authorTomasello, Giovanni
dc.contributor.authorBucchieri, Fabio
dc.contributor.authorConway de Macario, Everly
dc.contributor.authorMacario, Alberto J.L.
dc.contributor.departmentAnatomy, Cell Biology, and Physiological Sciences
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:36:46Z
dc.date.available2025-01-24T11:36:46Z
dc.date.issued2019
dc.description.abstractInflammatory bowel disease (IBD) encompasses various pathological conditions similar but distinct that share a multifactorial etiology, including involvement of the intestinal barrier function, the immune system, and intestinal microorganisms. Hsp60 is a chaperonin component of the chaperoning system, present in all cells and tissues, including the intestine. It plays important roles in cell physiology outside and inside mitochondria, its canonical place of residence. However, Hsp60 can also be pathogenic in many conditions, the Hsp60 chaperonopathies, possibly including IBD. The various clinico-pathological types of IBD have a complicated mix of causative factors, among which Hsp60 can be considered a putatively important driver of events and could play an etiopathogenic role. This possibility is discussed in this review. We also indicate that Hsp60 can be a biomarker useful in disease diagnosing and monitoring and, if found active in pathogenesis, should become a target for developing new therapies. The latter are particularly needed to alleviate patient suffering and to prevent complications, including colon cancer. Copyright © 2019 Cappello, Mazzola, Jurjus, Zeenny, Jurjus, Carini, Leone, Bonaventura, Tomasello, Bucchieri, Conway de Macario and Macario. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
dc.identifier.doihttps://doi.org/10.3389/fphar.2019.00026
dc.identifier.eid2-s2.0-85065907026
dc.identifier.urihttp://hdl.handle.net/10938/28715
dc.language.isoen
dc.publisherFrontiers Media S.A.
dc.relation.ispartofFrontiers in Pharmacology
dc.sourceScopus
dc.subjectChaperoning system
dc.subjectChaperonopathy
dc.subjectChaperonotherapy
dc.subjectHsp60
dc.subjectImmune system
dc.subjectInflammatory bowel disease
dc.subjectIntestinal wall
dc.subjectMicrobiota
dc.subjectBiological marker
dc.subjectChaperone
dc.subjectChaperonin
dc.subjectChaperonin 60
dc.subjectArticle
dc.subjectHuman
dc.subjectIntestine wall
dc.subjectMitochondrion
dc.subjectMolecular mechanics
dc.subjectNonhuman
dc.subjectPathogenesis
dc.subjectPatient monitoring
dc.subjectProtein function
dc.subjectProtein homeostasis
dc.subjectProtein targeting
dc.titleHsp60 as a novel target in IBD management: A prospect
dc.typeArticle

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