Cargando…
Candidate protein biomarkers in pancreatic neuroendocrine neoplasms grade 3
Pancreatic neuroendocrine neoplasms (PanNENs) are rare tumours that compose 1–2% of all pancreatic tumours. Patients with metastatic grade 3 neoplasia are usually treated with chemotherapy but have a poor progression-free and overall survival. According to the WHO 2017 classification, they are divid...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7327066/ https://www.ncbi.nlm.nih.gov/pubmed/32606315 http://dx.doi.org/10.1038/s41598-020-67670-7 |
_version_ | 1783552464973201408 |
---|---|
author | Ali, Abir Salwa Perren, Aurel Lindskog, Cecilia Welin, Staffan Sorbye, Halfdan Grönberg, Malin Janson, Eva Tiensuu |
author_facet | Ali, Abir Salwa Perren, Aurel Lindskog, Cecilia Welin, Staffan Sorbye, Halfdan Grönberg, Malin Janson, Eva Tiensuu |
author_sort | Ali, Abir Salwa |
collection | PubMed |
description | Pancreatic neuroendocrine neoplasms (PanNENs) are rare tumours that compose 1–2% of all pancreatic tumours. Patients with metastatic grade 3 neoplasia are usually treated with chemotherapy but have a poor progression-free and overall survival. According to the WHO 2017 classification, they are divided into neuroendocrine tumours (NETs) G3 and neuroendocrine carcinomas (NECs). Despite the new classification, new diagnostic and prognostic biomarkers are needed to sub-categorise the patients and to help guide therapy decisions. Blood from 42 patients and 42 healthy controls were screened for the presence of 92 proteins with the Immuno-Oncology panel using the Proximity Extension Assay provided by Olink Biosciences. Immunohistochemical staining of FAS ligand (FASLG) was performed on 16 patient tumour specimens using a commercial antibody. Fifty-four out of 87 evaluable proteins differed significantly in concentration between blood from patients and blood from healthy controls. FASLG was the only protein for which the concentration in blood was significantly lower in patients compared to controls and the levels correlated negatively to Ki-67 index. Seven of 14 evaluable PanNEN G3 specimens showed FASLG immunoreactivity in the tumour cells while there was scattered immunoreactivity in immune cells. Positive FASLG immunoreactivity correlated to well-differentiated morphology. FASLG concentration in blood was significantly lower in patients with pancreatic NENs G3 compared to controls, and the expression in tumour tissue was variable. Furthermore, FASLG was negatively correlated to Ki-67 and was more frequently expressed in well-differentiated tumours. Taken together, these results may suggest a role of FASLG in PanNENs. |
format | Online Article Text |
id | pubmed-7327066 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-73270662020-07-01 Candidate protein biomarkers in pancreatic neuroendocrine neoplasms grade 3 Ali, Abir Salwa Perren, Aurel Lindskog, Cecilia Welin, Staffan Sorbye, Halfdan Grönberg, Malin Janson, Eva Tiensuu Sci Rep Article Pancreatic neuroendocrine neoplasms (PanNENs) are rare tumours that compose 1–2% of all pancreatic tumours. Patients with metastatic grade 3 neoplasia are usually treated with chemotherapy but have a poor progression-free and overall survival. According to the WHO 2017 classification, they are divided into neuroendocrine tumours (NETs) G3 and neuroendocrine carcinomas (NECs). Despite the new classification, new diagnostic and prognostic biomarkers are needed to sub-categorise the patients and to help guide therapy decisions. Blood from 42 patients and 42 healthy controls were screened for the presence of 92 proteins with the Immuno-Oncology panel using the Proximity Extension Assay provided by Olink Biosciences. Immunohistochemical staining of FAS ligand (FASLG) was performed on 16 patient tumour specimens using a commercial antibody. Fifty-four out of 87 evaluable proteins differed significantly in concentration between blood from patients and blood from healthy controls. FASLG was the only protein for which the concentration in blood was significantly lower in patients compared to controls and the levels correlated negatively to Ki-67 index. Seven of 14 evaluable PanNEN G3 specimens showed FASLG immunoreactivity in the tumour cells while there was scattered immunoreactivity in immune cells. Positive FASLG immunoreactivity correlated to well-differentiated morphology. FASLG concentration in blood was significantly lower in patients with pancreatic NENs G3 compared to controls, and the expression in tumour tissue was variable. Furthermore, FASLG was negatively correlated to Ki-67 and was more frequently expressed in well-differentiated tumours. Taken together, these results may suggest a role of FASLG in PanNENs. Nature Publishing Group UK 2020-06-30 /pmc/articles/PMC7327066/ /pubmed/32606315 http://dx.doi.org/10.1038/s41598-020-67670-7 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Ali, Abir Salwa Perren, Aurel Lindskog, Cecilia Welin, Staffan Sorbye, Halfdan Grönberg, Malin Janson, Eva Tiensuu Candidate protein biomarkers in pancreatic neuroendocrine neoplasms grade 3 |
title | Candidate protein biomarkers in pancreatic neuroendocrine neoplasms grade 3 |
title_full | Candidate protein biomarkers in pancreatic neuroendocrine neoplasms grade 3 |
title_fullStr | Candidate protein biomarkers in pancreatic neuroendocrine neoplasms grade 3 |
title_full_unstemmed | Candidate protein biomarkers in pancreatic neuroendocrine neoplasms grade 3 |
title_short | Candidate protein biomarkers in pancreatic neuroendocrine neoplasms grade 3 |
title_sort | candidate protein biomarkers in pancreatic neuroendocrine neoplasms grade 3 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7327066/ https://www.ncbi.nlm.nih.gov/pubmed/32606315 http://dx.doi.org/10.1038/s41598-020-67670-7 |
work_keys_str_mv | AT aliabirsalwa candidateproteinbiomarkersinpancreaticneuroendocrineneoplasmsgrade3 AT perrenaurel candidateproteinbiomarkersinpancreaticneuroendocrineneoplasmsgrade3 AT lindskogcecilia candidateproteinbiomarkersinpancreaticneuroendocrineneoplasmsgrade3 AT welinstaffan candidateproteinbiomarkersinpancreaticneuroendocrineneoplasmsgrade3 AT sorbyehalfdan candidateproteinbiomarkersinpancreaticneuroendocrineneoplasmsgrade3 AT gronbergmalin candidateproteinbiomarkersinpancreaticneuroendocrineneoplasmsgrade3 AT jansonevatiensuu candidateproteinbiomarkersinpancreaticneuroendocrineneoplasmsgrade3 |