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Alpha retinal ganglion cells in pigmented mice retina: number and distribution

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dc.contributor.author Gallego-Ortega,Alejandro
dc.contributor.author Norte-Munoz,Maria
dc.contributor.author Di-Pierdomenico,Johnny
dc.contributor.author Aviles-Trigueros,Marcelino
dc.contributor.author de-la-Villa,Pedro
dc.contributor.author Javier-Valiente-Soriano,Francisco
dc.contributor.author Vidal-Sanz,Manuel
dc.date.accessioned 2025-10-20T14:38:04Z
dc.date.available 2025-10-20T14:38:04Z
dc.date.issued 01/12/2022
dc.identifier.citation Gallego-Ortega A, Norte-Muñoz M, Di Pierdomenico J, Avilés-Trigueros M, De La Villa P, Valiente-Soriano FJ, et al. Alpha retinal ganglion cells in pigmented mice retina: number and distribution. Front Neuroanat. 1 de diciembre de 2022;16:1054849.
dc.identifier.issn 1662-5129
dc.identifier.uri https://sms.carm.es/ricsmur/handle/123456789/20453
dc.description.abstract BackgroundUp to 30% of breast cancer (BC) patients treated with neoadjuvant chemotherapy (NCT) will relapse. Our objective was to analyze the predictive capacity of several markers associated with immune response and cell proliferation combined with clinical parameters. MethodsThis was a single-center, retrospective cohort study of BC patients treated with NCT (2001-2010), in whom pretreatment biomarkers were analyzed: neutrophil-to-lymphocyte ratio (NLR) in peripheral blood, CD3+ tumor-infiltrating lymphocytes (TILs), and gene expression of AURKA, MYBL2 and MKI67 using qRT-PCR. ResultsA total of 121 patients were included. Median followup was 12 years. In a univariate analysis, NLR, TILs, AURKA, and MYBL2 showed prognostic value for overall survival. In multivariate analyses, including hormone receptor, HER2 status, and response to NCT, NLR (HR 1.23, 95% CI 1.01-1.75), TILs (HR 0.84, 95% CI 0.73-0.93), AURKA (HR 1.05, 95% CI 1.00-1.11) and MYBL2 (HR 1.19, 95% CI 1.05-1.35) remained as independent predictor variables. ConclusionConsecutive addition of these biomarkers to a regression model progressively increased its discriminatory capacity for survival. Should independent cohort studies validate these findings, management of early BC patients may well be changed.
dc.language.iso eng
dc.publisher FRONTIERS MEDIA SA
dc.rights Atribución-NoComercial-SinDerivadas 3.0 España
dc.rights.uri http://creativecommons.org/licenses/by-nc-nd/3.0/es/ *
dc.title Alpha retinal ganglion cells in pigmented mice retina: number and distribution
dc.type info:eu-repo/semantics/article
dc.identifier.pmid 36530520
dc.relation.publisherversion https://dx.doi.org/10.3389/fnana.2022.1054849
dc.type.version info:eu-repo/semantics/publishedVersion
dc.identifier.doi 10.3389/fnana.2022.1054849
dc.journal.title Frontiers in Neuroanatomy


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Atribución-NoComercial-SinDerivadas 3.0 España Excepto si se señala otra cosa, la licencia del ítem se describe como Atribución-NoComercial-SinDerivadas 3.0 España

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