Study of the expression of cathepsins in histological material from pancreatic lesions


Por: Martinez, J, Ramon Aparicio, J, Peiro, G, Cabezas, A, Roger, M, Ruiz, F, Company, L and Antonio Casellas, J

Publicada: 1 dic 2016
Resumen:
Background and aims: To assess the expression levels of cathepsins in malignant and premalignant lesions. Methods: We retrospectively included patients who underwent pancreatic surgery on pancreatic solid or cystic masses. The expression of cathepsin H, L, B and S was determined in both types of samples. Lesions were divided into three categories: malignant (pancreatic adenocarcinoma and malignant mucinous neoplasms), premalignant (mucinous neoplasms) and benign (other lesions). Results: Thirty-one surgical resection samples were studied. The expression of cathepsins was significantly higher in malignant lesions than in premalignant and benign lesions (H 75%, 27%, 37% p = 0.05; L 92%, 36%, 37% p = 0.011; B 83%, 36%, 62% p = 0.069; S 92%, 36%, 25% p = 0.004, respectively). Conclusions: Cathepsins are overexpressed in histological samples of malignant lesions compared to premalignant and benign lesions. However, the expression of cathepsins is similar in both premalignant and benign lesions.

Filiaciones:
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 Hosp Gen Univ Alicante, Dept Digest Endoscopy, C Pintor Baeza S-N, Alicante 03010, Spain

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 Hosp Gen Univ Alicante, Dept Digest Endoscopy, C Pintor Baeza S-N, Alicante 03010, Spain

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 Hosp Gen Univ Alicante, Dept Anat Pathol, Alicante, Spain

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 Hosp Gen Univ Alicante, Dept Anat Pathol, Alicante, Spain

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 Hosp Gen Univ Alicante, Dept Digest Endoscopy, C Pintor Baeza S-N, Alicante 03010, Spain

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 Hosp Gen Univ Alicante, Dept Digest Endoscopy, C Pintor Baeza S-N, Alicante 03010, Spain

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 Hosp Gen Univ Alicante, Dept Digest Endoscopy, C Pintor Baeza S-N, Alicante 03010, Spain

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 Hosp Gen Univ Alicante, Dept Digest Endoscopy, C Pintor Baeza S-N, Alicante 03010, Spain
ISSN: 11300108





REVISTA ESPANOLA DE ENFERMEDADES DIGESTIVAS
Editorial
ARAN EDICIONES, S A, CASTELLO, 128, 1O, 28006 MADRID, SPAIN, España
Tipo de documento: Article
Volumen: 108 Número: 12
Páginas: 780-784
WOS Id: 000389125100005
ID de PubMed: 27855482
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