Epidermal Growth Factor Is Essential for the Maintenance of Novel Prostate Epithelial Cells Isolated From Patient-Derived Organoids

dc.contributor.authorCheaito, Katia A.
dc.contributor.authorBahmad, Hisham F.
dc.contributor.authorJalloul, Hiba A.
dc.contributor.authorHadadeh, Ola
dc.contributor.authorMsheik, Hiba
dc.contributor.authorEl Hajj, Albert Elias
dc.contributor.authorMukherji, Deborah M.
dc.contributor.authorAl-Sayegh, Mohamed Ahmed
dc.contributor.authorAbou-Kheir, Wassim G.
dc.contributor.departmentAnatomy, Cell Biology, and Physiological Sciences
dc.contributor.departmentSurgery
dc.contributor.departmentInternal Medicine
dc.contributor.departmentDivision of Urology
dc.contributor.departmentDivision of Hematology Oncology
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.abstractProstate cancer (PCa) is the second leading cause of cancer-related mortality and morbidity among males worldwide. Deciphering the biological mechanisms and molecular pathways involved in PCa pathogenesis and progression has been hindered by numerous technical limitations mainly attributed to the limited number of cell lines available, which do not recapitulate the diverse phenotypes of clinical disease. Indeed, PCa has proven problematic to establish as cell lines in culture due to its heterogeneity which remains a challenge, despite the various in vitro and in vivo model systems available. Growth factors have been shown to play a central role in the complex regulation of cell proliferation among hormone sensitive tumors, such as PCa. Here, we report the isolation and characterization of novel patient-derived prostate epithelial (which we named as AUB-PrC) cells from organoids culture system. We also assessed the role of epidermal growth factor (EGF) in culturing those cells. We profiled the AUB-PrC cells isolated from unaffected and tumor patient samples via depicting their molecular and epithelial lineage features through immunofluorescence staining and quantitative real-time PCR (qRT-PCR), as well as through functional assays and transcriptomic profiling through RNA sequencing. In addition, by optimizing a previously established prostate organoids culture system, we were able to grow human prostate epithelial cells using growth medium and EGF only. With these data collected, we were able to gain insight at the molecular architecture of novel human AUB-PrC cells, which might pave the way for deciphering the mechanisms that lead to PCa development and progression, and ultimately improving prognostic abilities and treatments. © Copyright © 2020 Cheaito, Bahmad, Jalloul, Hadadeh, Msheik, El-Hajj, Mukherji, Al-Sayegh and Abou-Kheir.
dc.identifier.doihttps://doi.org/10.3389/fcell.2020.571677
dc.identifier.eid2-s2.0-85096005552
dc.identifier.urihttp://hdl.handle.net/10938/28754
dc.language.isoen
dc.publisherFrontiers Media S.A.
dc.relation.ispartofFrontiers in Cell and Developmental Biology
dc.sourceScopus
dc.subjectEgf
dc.subjectLineage markers
dc.subjectOrganoids
dc.subjectProstate cancer
dc.subjectProstate epithelial cells
dc.subjectRna-seq
dc.subjectAndrogen receptor
dc.subjectCell adhesion molecule
dc.subjectCollagen type 1
dc.subjectCytokeratin 13
dc.subjectCytokeratin 14
dc.subjectCytokeratin 18
dc.subjectCytokeratin 19
dc.subjectCytokeratin 5
dc.subjectCytokeratin 8
dc.subjectDna binding protein
dc.subjectEpidermal growth factor
dc.subjectFibroblast growth factor 10
dc.subjectFibroblast growth factor 2
dc.subjectFibroblast growth factor receptor 1
dc.subjectHepatocyte nuclear factor 3alpha
dc.subjectHermes antigen
dc.subjectInterleukin 6
dc.subjectMessenger rna
dc.subjectMyc protein
dc.subjectNerve cell adhesion molecule
dc.subjectNeurotrophin 3
dc.subjectProtein p63
dc.subjectReactive oxygen metabolite
dc.subjectTranscription factor
dc.subjectTranscription factor e2f
dc.subjectTranscriptome
dc.subjectTwist related protein 1
dc.subjectUvomorulin
dc.subjectVimentin
dc.subjectAdult
dc.subjectArticle
dc.subjectCancer growth
dc.subjectCell culture
dc.subjectCell growth
dc.subjectCell isolation
dc.subjectCell lineage
dc.subjectCell migration
dc.subjectCell proliferation
dc.subjectCell viability
dc.subjectCholesterol metabolism
dc.subjectControlled study
dc.subjectDna microarray
dc.subjectDown regulation
dc.subjectExtracellular matrix
dc.subjectGene expression
dc.subjectGene expression profiling
dc.subjectGenetic background
dc.subjectGenetic fingerprinting
dc.subjectGleason score
dc.subjectHuman
dc.subjectHuman cell
dc.subjectHuman tissue
dc.subjectImmunofluorescence
dc.subjectIn vitro study
dc.subjectMale
dc.subjectMrna expression level
dc.subjectMtt assay
dc.subjectNeural crest cell
dc.subjectNotch signaling
dc.subjectOrganoid
dc.subjectPhenotype
dc.subjectProstate adenocarcinoma
dc.subjectProstate epithelium cell
dc.subjectReal time polymerase chain reaction
dc.subjectRna extraction
dc.subjectRna purification
dc.subjectRna sequencing
dc.subjectSensation
dc.subjectSequence analysis
dc.subjectSignal transduction
dc.subjectTranscription regulation
dc.subjectTranscriptomics
dc.subjectUpregulation
dc.titleEpidermal Growth Factor Is Essential for the Maintenance of Novel Prostate Epithelial Cells Isolated From Patient-Derived Organoids
dc.typeArticle

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