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Journal of Korean Medical Science ; : 1154-1160, 2013.
Article Dans Anglais | WPRIM | ID: wpr-173142

Résumé

15-Hydroxyprostaglandin dehydrogenase (15-PGDH) is downregulated during the early stages of colorectal carcinogenesis. The aim of the present study was to investigate the potential role of 15-PGDH in normal-appearing colorectal mucosa as a biomarker for predicting colorectal neoplasms. We obtained paired tumor and normal tissues from the surgical specimens of 32 sporadic colorectal cancer patients. mRNA expression of 15-PGDH was measured using a quantitative real-time PCR assay. We evaluated the association between 15-PGDH mRNA expression in normal-appearing mucosa, the presence of synchronous adenoma, and the cumulative incidence of metachronous adenoma. The relative 15-PGDH expression of normal-appearing mucosa in patients with synchronous adenoma was significantly lower than in patients without synchronous adenoma (0.71 vs 1.00, P = 0.044). The patients in the lowest tertile of 15-PGDH expression in normal-appearing mucosa were most likely to have synchronous adenoma (OR: 10.5, P = 0.024). Patients with low 15-PGDH expression in normal-appearing mucosa also demonstrated more advanced stage colorectal cancer (P = 0.045). However, there was no significant difference in the cumulative incidence of metachronous adenoma according to 15-PGDH mRNA expression in normal-appearing mucosa (P = 0.333). Hence, 15-PGDH in normal-appearing colorectal mucosa can be a useful biomarker of field effect for the prediction of sporadic synchronous neoplasms.


Sujets)
Sujet âgé , Femelle , Humains , Mâle , Adulte d'âge moyen , Tumeurs colorectales/diagnostic , Régulation négative , Hydroxyprostaglandine dehydrogenases/génétique , Muqueuse intestinale/enzymologie , Stadification tumorale , Tumeurs primitives multiples/enzymologie , Seconde tumeur primitive/enzymologie , Odds ratio , Valeur prédictive des tests , ARN messager/métabolisme , Réaction de polymérisation en chaine en temps réel , Facteurs de risque , Marqueurs biologiques tumoraux/métabolisme
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