Please use this identifier to cite or link to this item: https://saber.ucv.ve/jspui/handle/10872/15680
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dc.contributor.authorPaniz Mondolfi, Alberto E.-
dc.contributor.authorJour, George-
dc.contributor.authorJohnson, Matthew-
dc.contributor.authorReidy, Jason-
dc.contributor.authorCason, Ronald C.-
dc.contributor.authorBarkoh, Bedia A.-
dc.contributor.authorBenaím, Gustavo-
dc.contributor.authorSingh, Rajesh-
dc.contributor.authorLuthra, Raja-
dc.date.accessioned2017-04-18T15:24:30Z-
dc.date.available2017-04-18T15:24:30Z-
dc.date.issued2013-11-06-
dc.identifier.issn0046-8177-
dc.identifier.otherhttp://dx.doi.org/10.1016/j.humpath.2013.07.014-
dc.identifier.urihttp://hdl.handle.net/10872/15680-
dc.descriptionCorresponding author. Baylor College of Medicine, Department of Pathology and Immunology, Texas Children's Hospital. Houston, TX 77030, USA. E-mail address: albertopanizm@gmail.com (A. E. Paniz Mondolfi).en_US
dc.description.abstractPrimary cutaneous carcinosarcoma is a rare biphenotypic neoplasm exhibiting both epithelial and sarcomatous elements. Even though its origin and biological aspects remain poorly understood, it has been postulated that this tumor may arise from progenitor cells which subsequently differentiate into distinct tumor components. We have investigated the histological and immunohistochemical staining patterns of a cutaneous carcinosarcoma case, as well as its ultrastructural aspects. In addition, sarcomatous and epithelial tumor components were separated by laser capture microdissection and subjected to targeted, high-depth, Next-Generation Sequencing of a 46-cancer gene panel to asses the gene mutational pattern amongst both components. There were transitional cells at the epithelial/ mesenchymal transition which labeled with putative progenitor cell markers (K 19, c-kit, CD34 and BCL-2). There was shared reactivity to antibodies directed against the progenitor cell marker EpCAM (epithelial cell adhesion molecule) in both components. Ultrastructurally, individual cells were demonstrated to have overlapping features of epithelial and mesenchymal differentiation. The mutational analysis revealed point mutations in exon 5 of TP53 which were identical in both the epithelial and sarcomatous components, and which was concordant with p53 expression at a tissue level. The aforementioned histological, ultrastructural, immunohistochemical and mutational pattern is strongly suggestive of a common clonal origin to the distinct elements of this tumor.en_US
dc.language.isoenen_US
dc.publisherHuman Pathologyen_US
dc.relation.ispartofseriesVol. 44;No. 12 pp. 2853-2860-
dc.subjectCarcinosarcomaen_US
dc.subjectCutaneousen_US
dc.subjectBiphenotypic tumorsen_US
dc.subjectCancer stem cellsen_US
dc.subjectTumorigenesisen_US
dc.subjectMutationen_US
dc.subjectTP53en_US
dc.subjectNext generationen_US
dc.subjectsequencingen_US
dc.subjectbiphenotypic neoplasmen_US
dc.titlePrimary cutaneous carcinosarcoma: insights into its clonal origin and mutational pattern expression analysis through next generation sequencingen_US
dc.typeArticleen_US
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