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dc.contributor.authorDonizy, Piotr
dc.contributor.authorWu, Cheng-Lin
dc.contributor.authorMull, Jason
dc.contributor.authorFujimoto, Masakazu
dc.contributor.authorChłopik, Agata
dc.contributor.authorPeng, Yan
dc.contributor.authorShalin, Sara C.
dc.contributor.authorSelim, M. Angelica
dc.contributor.authorPuig, Susana
dc.contributor.authorFernandez Figueras, Maria-Teresa
dc.contributor.authorShea, Christopher R.
dc.contributor.authorBiernat, Wojciech
dc.contributor.authorRys, Janusz
dc.contributor.authorMarszalek, Andrzej
dc.contributor.authorHoang, Mai P.
dc.date.accessioned2021-09-03T15:45:43Z
dc.date.available2021-09-03T15:45:43Z
dc.date.issued2020
dc.identifier.citationDonizy, Piotr; Wu, Cheng-Lin; Mull, Jason [et al.]. Up-regulation of PARP1 expression significantly correlated with poor survival in mucosal melanomas. Cells, 2020, 9(5), 1135. Disponible en: <https://www.mdpi.com/2073-4409/9/5/1135>. Fecha de acceso: 3 sep. 2021. DOI: 10.3390/cells9051135ca
dc.identifier.issn2073-4409ca
dc.identifier.urihttp://hdl.handle.net/20.500.12328/2755
dc.description.abstractIntroduction: Mucosal melanoma is rare and associated with poorer prognosis in comparison to conventional melanoma subtypes. Little is known about the prognostic significance as well as possible associations between PARP1 and immunologic response in mucosal melanoma. Methods: PARP1, PD-L1 and IDO1 immunostains were performed on 192 mucosal melanomas including 86 vulvar, 89 sinonasal, and 17 anorectal melanomas. Results: By Kaplan–Meier analyses, high PARP1 expression correlated with worse overall and melanoma-specific survival (log-rank p values = 0.026 and 0.047, respectively). Tumors with combined PARP1 and IDO1 high expression correlated with worse overall and melanoma-specific survival (p = 0.015, 0.0034 respectively). By multivariate analyses, high PARP1 expression remained a predictor of worse survival independent of stage. By Fisher’s exact test, high PARP1 expression correlated with highly mitogenic tumors (p = 0.02). High tumoral PD-L1 and IDO1 expression were associated with ulcerated primary tumors (p = 0.019, 0.0019, respectively). By linear regression analyses, correlations between PARP1 expression versus IDO1 expression (p = 0.0001) and mitotic index (p = 0.0052) were observed. Conclusion: Increased expression of PARP1 is an independent negative prognostic marker in mucosal melanomas. The association between PARP1 and IDO1 and their combined adverse prognostic role raise the potential of combined therapy in mucosal melanoma.en
dc.format.extent12ca
dc.language.isoengca
dc.publisherMDPIca
dc.relation.ispartofCellsca
dc.relation.ispartofseries9;5
dc.rightsThis is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.en
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subject.otherMelanoma de la mucosaca
dc.subject.otherMelanoma vulvarca
dc.subject.otherMelanoma sinonasalca
dc.subject.otherMelanoma anorectalca
dc.subject.otherPARPca
dc.subject.otherIDO1ca
dc.subject.otherPronòsticca
dc.subject.otherNeoplàsiaca
dc.subject.otherMelanoma mucosoes
dc.subject.otherMelanoma vulvares
dc.subject.otherMelanoma nasosinusales
dc.subject.otherMelanoma anorrectales
dc.subject.otherPARPes
dc.subject.otherIDO1es
dc.subject.otherPronósticoes
dc.subject.otherNeoplasiaes
dc.subject.otherMucosal melanomaen
dc.subject.otherVulvar melanomaen
dc.subject.otherSinonasal melanomaen
dc.subject.otherAnorectal melanomaen
dc.subject.otherPARPen
dc.subject.otherIDO1en
dc.subject.otherPrognosisen
dc.subject.otherNeoplasiaen
dc.titleUp-regulation of PARP1 expression significantly correlated with poor survival in mucosal melanomasen
dc.typeinfo:eu-repo/semantics/articleca
dc.description.versioninfo:eu-repo/semantics/publishedVersionca
dc.rights.accessLevelinfo:eu-repo/semantics/openAccess
dc.embargo.termscapca
dc.subject.udc61ca
dc.identifier.doihttps://dx.doi.org/10.3390/cells9051135ca


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This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Except where otherwise noted, this item's license is described as https://creativecommons.org/licenses/by/4.0/
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