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1.
Br J Cancer ; 110(12): 2935-44, 2014 Jun 10.
Artículo en Inglés | MEDLINE | ID: mdl-24786601

RESUMEN

BACKGROUND: Tumour aggressiveness might be related to the degree of main cancer hallmark acquirement of tumour cells, reflected by expression levels of specific biomarkers. We investigated the expression of Aldh1, Survivin, and EpCAM, together reflecting main cancer hallmarks, in relation to clinical outcome of colorectal cancer (CRC) patients. METHODS: Immunohistochemistry was performed using a tumour tissue microarray of TNM (Tumour, Node, Metastasis)-stage I-IV CRC tissues. Single-marker expression or their combination was assessed for associations with the clinical outcome of CRC patients (N=309). RESULTS: Increased expression of Aldh1 or Survivin, or decreased expression of EpCAM was each associated with poor clinical outcome, and was therefore identified as clinically unfavourable expression. Analyses of the combination of all three markers showed worse clinical outcome, specifically in colon cancer patients, with an increasing number of markers showing unfavourable expression. Hazard ratios ranged up to 8.3 for overall survival (P<0.001), 36.6 for disease-specific survival (P<0.001), and 27.1 for distant recurrence-free survival (P<0.001). CONCLUSIONS: Our data identified combined expression levels of Aldh1, Survivin, and EpCAM as strong independent prognostic factors, with high hazard ratios, for survival and tumour recurrence in colon cancer patients, and therefore reflect tumour aggressiveness.


Asunto(s)
Antígenos de Neoplasias/biosíntesis , Biomarcadores de Tumor/biosíntesis , Moléculas de Adhesión Celular/biosíntesis , Neoplasias Colorrectales/patología , Proteínas Inhibidoras de la Apoptosis/biosíntesis , Isoenzimas/biosíntesis , Retinal-Deshidrogenasa/biosíntesis , Anciano , Familia de Aldehído Deshidrogenasa 1 , Neoplasias Colorrectales/metabolismo , Neoplasias Colorrectales/mortalidad , Molécula de Adhesión Celular Epitelial , Femenino , Regulación Neoplásica de la Expresión Génica , Humanos , Masculino , Persona de Mediana Edad , Metástasis de la Neoplasia , Pronóstico , Survivin , Análisis de Matrices Tisulares
2.
Nucleosides Nucleotides Nucleic Acids ; 23(8-9): 1381-4, 2004 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-15571263

RESUMEN

In a panel of 18 colon cancer cell lines we found that the thymidylate synthase (TS) genotype was related to TS enzyme activity, but not to TS protein and mRNA levels. In addition, no relation with drug sensitivity was observed. TS genotyping of different tissues from 78 colorectal cancer patients revealed a high level of homology in polymorphic status between normal and malignant tissues and the heterozygous genotype to be the most frequent.


Asunto(s)
Neoplasias del Colon/enzimología , Neoplasias del Colon/genética , Polimorfismo Genético , Timidilato Sintasa/biosíntesis , Timidilato Sintasa/genética , Antimetabolitos Antineoplásicos/farmacología , Línea Celular Tumoral , Resistencia a Antineoplásicos , Fluorouracilo/farmacología , Genotipo , Heterocigoto , Humanos , ARN Mensajero/metabolismo , Distribución Tisular
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