Molecular chaperones in tumors of salivary glands

dc.contributor.authorBasset, Charbel A.
dc.contributor.authorCappello, Francesco
dc.contributor.authorRappa, Francesca
dc.contributor.authorLentini, Vincenzo Luca
dc.contributor.authorJurjus, Abdo R.
dc.contributor.authorConway de Macario, Everly
dc.contributor.authorMacario, Alberto J.L.
dc.contributor.authorLeone, Angelo
dc.contributor.departmentAnatomy, Cell Biology, and Physiological Sciences
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:36:54Z
dc.date.available2025-01-24T11:36:54Z
dc.date.issued2020
dc.description.abstractThe salivary glands are key components of the mouth and play a central role in its physiology. Their importance may be appreciated considering their number, occurrence in pairs, and distribution in the mouth: two parotids, two submandibular, two sublingual, and many other small ones scattered throughout the mouth. They produce saliva, without which ingestion of non-liquid nutrients and speech would be practically impossible. Nevertheless, the physiology and pathology of salivary glands are poorly understood. For instance, tumors of salivary glands occur, and their incidence is on the rise, but their etiology and pathogenesis are virtually unknown, although some risk factors have been identified. Likewise, the role of the chaperoning system in the development, normal functioning, and pathology, including carcinogenesis, remains to be determined. This scarcity of basic knowledge impedes progress in diagnosis, disease monitoring, and therapeutics of salivary gland tumors. We are currently involved in examining the chaperoning system of human salivary glands and we performed a search of the literature to determine what has been reported relating to oncology. We found data pertaining to six components of the chaperone system, namely HSP27, HSP60, HSP70, HSP84, HSP86, and GRP78, and to another HSP, the heme-oxygenase H-O1, also named HSP32, which does not belong in the chaperoning system but seemed to have potential as a biomarker for diagnostic purposes as much as the HSP/chaperones mentioned above. The reported quantitative variations of the six chaperones were distinctive enough to distinguish malignant from benign tumors, suggesting that these molecules hold potential as biomarkers useful in differential diagnosis. Also, the quantitative variations described accompanying tumor development, as observed in cancers of other organs, encourages research to elucidate whether chaperones play a role in the initiation and/or progression of salivary gland tumors. © 2020, Springer Nature B.V.
dc.identifier.doihttps://doi.org/10.1007/s10735-020-09871-y
dc.identifier.eid2-s2.0-85083524777
dc.identifier.pmid32300923
dc.identifier.urihttp://hdl.handle.net/10938/28752
dc.language.isoen
dc.publisherSpringer
dc.relation.ispartofJournal of Molecular Histology
dc.sourceScopus
dc.subjectChaperoning system
dc.subjectDifferential diagnosis
dc.subjectHsp
dc.subjectMolecular chaperones
dc.subjectSalivary glands
dc.subjectTumorigenesis
dc.subjectTumors
dc.subjectAnimals
dc.subjectCell transformation, neoplastic
dc.subjectDisease susceptibility
dc.subjectHumans
dc.subjectSalivary gland neoplasms
dc.subjectChaperone
dc.subjectChaperonin 60
dc.subjectGlucose regulated protein 78
dc.subjectHeat shock protein 27
dc.subjectHeat shock protein 70
dc.subjectHeat shock protein 84
dc.subjectHeat shock protein 86
dc.subjectHeme oxygenase 1
dc.subjectUnclassified drug
dc.subjectCarcinogenesis
dc.subjectHuman
dc.subjectPathogenesis
dc.subjectPriority journal
dc.subjectReview
dc.subjectSalivary gland
dc.subjectSalivary gland tumor
dc.subjectAnimal
dc.subjectCell transformation
dc.subjectDisease predisposition
dc.subjectGenetics
dc.subjectMetabolism
dc.subjectPathology
dc.titleMolecular chaperones in tumors of salivary glands
dc.typeReview

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