Pancreatic ductal adenocarcinoma (PDAC) is an increasing cause of cancer-related death, due to its biologic aggressiveness and the lack of effective treatments. The cell membrane plays a significant role in carcinogenesis, expressing components that mediate the interaction with the peritumoral environment. The aims of our study were to evaluate the expression of six membrane components (CA 19-9, mucin 1 and 4 (MUC1, MUC4), mesothelin (MSLN), Glypican-1 (GPC-1), and Annexin A10 (ANXA10)) on 50 surgical samples of patients with PDAC and correlate it with the oncologic outcomes. The expression was assessed using the histo-score (H-score), a quantitative method based on immunostaining, on tumoral and peritumoral tissues. CA 19-9 and MUC1 showed an intense expression on tumor cells and a lower expression on pancreatic acini and ducts. Moreover, a high intensity of CA 19-9 correlated with a worse prognosis. MUC4, MSLN, GPC-1, and ANXA10 were selectively expressed by PDAC cells and may be potential biomarkers of the disease.(1) Background: Pancreatic ductal adenocarcinoma (PDAC) is one of the most lethal malignancies. The lack of validated disease biomarkers makes timely diagnosis challenging in most cases. Cell membrane and surface proteins play a crucial role in several routes of oncogenesis. The aim of this study was to evaluate the expression of six membrane antigens on PDAC (CA 19-9, mucin 1 and 4 (MUC1, MUC4), mesothelin (MSLN), Annexin A10 (ANXA10), Glypican-1 (GPC-1)) and their correlation with oncologic outcomes. (2) Methods: Immunohistochemical staining for CA 19.9, MUC1, MUC4, MSLN, ANXA10, and GPC-1 of surgical samples of 50 consecutive patients with PDAC was performed. Antigen expression for tumor, ductal, and acinar tissues was classified according to the histo-score (H-score) by two pathologists. (3) Results: Recurrence rate was 47% and 18 patients (36%) deceased (median follow-up 21.5 months). Immunostaining for CA 19-9 and MUC1 showed a significantly higher expression in the neoplastic tissue compared to non-tumor ductal and acinar tissues (p < 0.001). MUC4, MSLN, ANXA10, and GPC-1 were selectively expressed in the neoplastic tissue (p < 0.001). A CA 19-9 H-score value >270 was independently associated with a worse overall survival (p = 0.05) and disease-free survival (p = 0.05). (4) Conclusions: CA 19-9 and MUC1 are highly expressed in PDAC cells. The histological expression of CA 19-9 may predict prognosis. MUC4, MSLN, ANXA10, and GPC-1 are selectively expressed by neoplastic tissue and may represent a potential histological biomarker of disease.

Nicoletti, A., Vitale, F., Quero, G., Paratore, M., Fiorillo, C., Negri, M., Carlino, A., Inzani, F., Gasbarrini, A., Alfieri, S., Zileri Dal Verme, L., Immunohistochemical Evaluation of the Expression of Specific Membrane Antigens in Patients with Pancreatic Ductal Adenocarcinoma, <<CANCERS>>, 2023; 15 (18): N/A-N/A. [doi:10.3390/cancers15184586] [https://hdl.handle.net/10807/260332]

Immunohistochemical Evaluation of the Expression of Specific Membrane Antigens in Patients with Pancreatic Ductal Adenocarcinoma

Nicoletti, Alberto;Vitale, Federica;Quero, Giuseppe;Paratore, Mattia;Fiorillo, Claudio;Negri, Marcantonio;Inzani, Frediano;Gasbarrini, Antonio
;
Alfieri, Sergio;Zileri Dal Verme, Lorenzo
2023

Abstract

Pancreatic ductal adenocarcinoma (PDAC) is an increasing cause of cancer-related death, due to its biologic aggressiveness and the lack of effective treatments. The cell membrane plays a significant role in carcinogenesis, expressing components that mediate the interaction with the peritumoral environment. The aims of our study were to evaluate the expression of six membrane components (CA 19-9, mucin 1 and 4 (MUC1, MUC4), mesothelin (MSLN), Glypican-1 (GPC-1), and Annexin A10 (ANXA10)) on 50 surgical samples of patients with PDAC and correlate it with the oncologic outcomes. The expression was assessed using the histo-score (H-score), a quantitative method based on immunostaining, on tumoral and peritumoral tissues. CA 19-9 and MUC1 showed an intense expression on tumor cells and a lower expression on pancreatic acini and ducts. Moreover, a high intensity of CA 19-9 correlated with a worse prognosis. MUC4, MSLN, GPC-1, and ANXA10 were selectively expressed by PDAC cells and may be potential biomarkers of the disease.(1) Background: Pancreatic ductal adenocarcinoma (PDAC) is one of the most lethal malignancies. The lack of validated disease biomarkers makes timely diagnosis challenging in most cases. Cell membrane and surface proteins play a crucial role in several routes of oncogenesis. The aim of this study was to evaluate the expression of six membrane antigens on PDAC (CA 19-9, mucin 1 and 4 (MUC1, MUC4), mesothelin (MSLN), Annexin A10 (ANXA10), Glypican-1 (GPC-1)) and their correlation with oncologic outcomes. (2) Methods: Immunohistochemical staining for CA 19.9, MUC1, MUC4, MSLN, ANXA10, and GPC-1 of surgical samples of 50 consecutive patients with PDAC was performed. Antigen expression for tumor, ductal, and acinar tissues was classified according to the histo-score (H-score) by two pathologists. (3) Results: Recurrence rate was 47% and 18 patients (36%) deceased (median follow-up 21.5 months). Immunostaining for CA 19-9 and MUC1 showed a significantly higher expression in the neoplastic tissue compared to non-tumor ductal and acinar tissues (p < 0.001). MUC4, MSLN, ANXA10, and GPC-1 were selectively expressed in the neoplastic tissue (p < 0.001). A CA 19-9 H-score value >270 was independently associated with a worse overall survival (p = 0.05) and disease-free survival (p = 0.05). (4) Conclusions: CA 19-9 and MUC1 are highly expressed in PDAC cells. The histological expression of CA 19-9 may predict prognosis. MUC4, MSLN, ANXA10, and GPC-1 are selectively expressed by neoplastic tissue and may represent a potential histological biomarker of disease.
2023
Inglese
Nicoletti, A., Vitale, F., Quero, G., Paratore, M., Fiorillo, C., Negri, M., Carlino, A., Inzani, F., Gasbarrini, A., Alfieri, S., Zileri Dal Verme, L., Immunohistochemical Evaluation of the Expression of Specific Membrane Antigens in Patients with Pancreatic Ductal Adenocarcinoma, <<CANCERS>>, 2023; 15 (18): N/A-N/A. [doi:10.3390/cancers15184586] [https://hdl.handle.net/10807/260332]
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