Please use this identifier to cite or link to this item: https://hdl.handle.net/10216/111875
Author(s): Balmaña, M
Duran, A
Gomes, C
Llop, E
López-Martos, R
Ortiz, MR
Barrabés, S
Reis, CA
Peracaula, R
Title: Analysis of sialyl-Lewis x on MUC5AC and MUC1 mucins in pancreatic cancer tissues
Publisher: Elsevier
Issue Date: 2018
Abstract: Pancreatic adenocarcinoma (PDAC) lacks efficient biomarkers. Mucins are glycoproteins that can carry aberrant glycosylation in cancer. Our objective was to identify cancer-related glycan epitopes on MUC1 and MUC5AC mucins in PDAC as potential biomarkers. We have analysed the tumour-associated carbohydrate antigens sialyl-Lewis x (SLex) and sialyl-Tn (STn) on MUC1 and MUC5AC in PDAC tissues. The selected cohort for this study consisted of twenty-one PDAC tissues positive for SLex antigen and three normal pancreas specimens as controls. STn expression was shown in 76% of the PDAC tissues. MUC1 and MUC5AC were detected in 90% of PDAC tissues. We performed in situ proximity ligation assay combining antibodies against mucins and glycan epitopes to identify specific mucin glycoforms. MUC1-SLex and MUC5AC-SLex were found in 68% and 84% respectively, of the mucin expressing PDAC tissues, while STn hardly colocalized with any of the evaluated mucins. Further analysis by Western blot of MUC5AC and SLex in eight PDAC tissue lysates showed that six out of eight cases were positive for both markers. Moreover, immunoprecipitation of MUC5AC from positive PDAC tissues and subsequent SLex immunodetection confirmed the presence of SLex on MUC5AC. Altogether, MUC5AC-SLex glycoform is present in PDAC and can be regarded as potential biomarker.
Subject: Mucins
Pancreatic cancer
Sialyl-Lewis x
URI: http://hdl.handle.net/10216/111875
Series: International journal of biological macromolecules, vol. 112, p. 33-45
Document Type: Artigo em Revista Científica Internacional
Rights: embargoedAccess
License: https://creativecommons.org/licenses/by-nc-nd/3.0/pt/
Embargo End Date: 2019-06-30
Appears in Collections:I3S - Artigo em Revista Científica Internacional

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