Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/90731
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dc.contributor.authorBurke, M.-
dc.contributor.authorMorais, C.-
dc.contributor.authorOliver, K.-
dc.contributor.authorLambie, D.-
dc.contributor.authorGobe, G.-
dc.contributor.authorCarroll, R.-
dc.contributor.authorStaatz, C.-
dc.contributor.authorSinnya, S.-
dc.contributor.authorSoyer, H.-
dc.contributor.authorWinterford, C.-
dc.contributor.authorHaass, N.-
dc.contributor.authorCampbell, S.-
dc.contributor.authorIsbel, N.-
dc.date.issued2015-
dc.identifier.citationAmerican Journal of Clinical Pathology, 2015; 143(4):514-526-
dc.identifier.issn0002-9173-
dc.identifier.issn1943-7722-
dc.identifier.urihttp://hdl.handle.net/2440/90731-
dc.description.abstractObjectives: This study aims to investigate how immunosuppression influences the protein expression of antiapoptotic members of the Bcl-2 family—namely, Bcl-xL and Mcl-1—in nonmelanoma skin cancer (NMSC) and the peritumoral epidermis of renal transplant recipients. Methods: NMSC and peritumoral epidermis protein expression of Bcl-xL and Mcl-1 were assessed by immunohistochemistry in renal transplant recipients receiving tacrolimus or sirolimus and the general population not receiving immunosuppression. Results: NMSC from renal transplant recipients compared with patients not receiving immunosuppressant medications had a reduced Bcl-xL expression intensity (P = .042). Mcl-1 expression intensity in NMSC was decreased in tacrolimus-treated patients compared with sirolimus-treated patients and the nonimmunosuppressed population (P = .024). Bcl-xL expression intensity was increased in peritumoral epidermis compared with NMSC (P = .002). Conclusions: It was shown for the first time that Bcl-xL and Mcl-1 expression are widespread in the peritumoral epidermis and NMSC of renal transplant recipients. Importantly in NMSC, Bcl-xL expression was reduced with immunosuppression exposure, and Mcl-1 expression was reduced in tacrolimus-treated compared with sirolimustreated patients.-
dc.description.statementofresponsibilityMichael T. Burke, Christudas Morais, Kimberley A. Oliver, Duncan L. J. Lambie, Glenda C. Gobe, Robert P. Carroll, Christine E. Staatz, Sudipta Sinnya, H. Peter Soyer, Clay Winterford, Nikolas K. Haass, Scott B. Campbell and Nicole M. Isbel-
dc.language.isoen-
dc.publisherLippincott, Williams & Wilkins-
dc.rights© 2015 by The American Society for Clinical Pathology-
dc.source.urihttp://dx.doi.org/10.1309/ajcpqnb5wa3plqbk-
dc.subjectHumans-
dc.subjectCarcinoma, Basal Cell-
dc.subjectCarcinoma, Squamous Cell-
dc.subjectSkin Neoplasms-
dc.subjectSirolimus-
dc.subjectTacrolimus-
dc.subjectImmunosuppressive Agents-
dc.subjectKidney Transplantation-
dc.subjectImmunohistochemistry-
dc.subjectMitosis-
dc.subjectApoptosis-
dc.subjectAdult-
dc.subjectAged-
dc.subjectAged, 80 and over-
dc.subjectMiddle Aged-
dc.subjectFemale-
dc.subjectMale-
dc.subjectbcl-X Protein-
dc.subjectMyeloid Cell Leukemia Sequence 1 Protein-
dc.subjectTransplant Recipients-
dc.titleExpression of Bcl-xL and Mcl-1 in the nonmelanoma skin cancers of renal transplant recipients-
dc.typeJournal article-
dc.identifier.doi10.1309/AJCPQNB5WA3PLQBK-
pubs.publication-statusPublished-
dc.identifier.orcidCarroll, R. [0000-0002-6238-026X]-
Appears in Collections:Aurora harvest 7
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