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The value of desmosomal plaque-related markers to distinguish squamous cell carcinoma and adenocarcinoma of the lung.
Galindo, Inmaculada; Gómez-Morales, Mercedes; Díaz-Cano, Inés; Andrades, Álvaro; Caba-Molina, Mercedes; Miranda-León, María Teresa; Medina, Pedro Pablo; Martín-Padron, Joel; Fárez-Vidal, María Esther.
Afiliación
  • Galindo I; Department of Pathology, School of Medicine, University of Granada, Granada, Spain.
  • Gómez-Morales M; Department of Pathology, School of Medicine, University of Granada, Granada, Spain.
  • Díaz-Cano I; Department of Biochemistry and Molecular Biology III, School of Medicine, University of Granada, Granada, Spain.
  • Andrades Á; Centre for Genomics and Oncological Research (GENYO), Granada, Spain.
  • Caba-Molina M; Institute for Biomedical Research (IBS Granada), University Hospital Complex of Granada/University of Granada, Granada, Spain.
  • Miranda-León MT; Centre for Genomics and Oncological Research (GENYO), Granada, Spain.
  • Medina PP; Department of Biochemistry and Molecular Biology I, University of Granada, Granada, Spain.
  • Martín-Padron J; Department of Pathology, School of Medicine, University of Granada, Granada, Spain.
  • Fárez-Vidal ME; Department of Statistics and Operative Research, School of Medicine, University of Granada, Granada, Spain.
Ups J Med Sci ; 125(1): 19-29, 2020 Feb.
Article en En | MEDLINE | ID: mdl-31809668
ABSTRACT

Background:

An antibody panel is needed to definitively differentiate between adenocarcinoma (AC) and squamous cell carcinoma (SCC) in order to meet more stringent requirements for the histologic classification of lung cancers. Staining of desmosomal plaque-related proteins may be useful in the diagnosis of lung SCC.Materials and

methods:

We compared the usefulness of six conventional (CK5/6, p40, p63, CK7, TTF1, and Napsin A) and three novel (PKP1, KRT15, and DSG3) markers to distinguish between lung SCC and AC in 85 small biopsy specimens (41 ACs and 44 SCCs). Correlations were examined between expression of the markers and patients' histologic and clinical data.

Results:

The specificity for SCC of membrane staining for PKP1, KRT15, and DSG3 was 97.4%, 94.6%, and 100%, respectively, and it was 100% when the markers were used together and in combination with the conventional markers (AUCs of 0.7619 for Panel 1 SCC, 0.7375 for Panel 2 SCC, 0.8552 for Panel 1 AC, and 0.8088 for Panel 2 AC). In a stepwise multivariate logistic regression model, the combination of CK5/6, p63, and PKP1 in membrane was the optimal panel to differentiate between SCC and AC, with a percentage correct classification of 96.2% overall (94.6% of ACs and 97.6% of SCCs). PKP1 and DSG3 are related to the prognosis.

Conclusions:

PKP1, KRT15, and DSG3 are highly specific for SCC, but they were more useful to differentiate between SCC and AC when used together and in combination with conventional markers. PKP1 and DSG3 expressions may have prognostic value.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Carcinoma de Células Escamosas / Adenocarcinoma / Biomarcadores de Tumor / Desmosomas / Neoplasias Pulmonares Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Female / Humans / Male / Middle aged Idioma: En Revista: Ups J Med Sci Año: 2020 Tipo del documento: Article País de afiliación: España

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Carcinoma de Células Escamosas / Adenocarcinoma / Biomarcadores de Tumor / Desmosomas / Neoplasias Pulmonares Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Female / Humans / Male / Middle aged Idioma: En Revista: Ups J Med Sci Año: 2020 Tipo del documento: Article País de afiliación: España