Cargando…
PGP 9.5 immunocytochemical staining for pancreatic endocrine tumors
Aims/hypothesis: Protein gene product 9.5 (PGP 9.5) is a marker for neuroendocrine cells but has not been used for pancreatic islet cells and pancreatic endocrine tumors (PETs). Antibodies for PGP 9.5 are now commercially available for immunocytochemical study, with which immunostaining may be able...
Autor principal: | |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Landes Bioscience
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4049838/ https://www.ncbi.nlm.nih.gov/pubmed/23959334 http://dx.doi.org/10.4161/isl.25351 |
_version_ | 1782319880951824384 |
---|---|
author | Tomita, Tatsuo |
author_facet | Tomita, Tatsuo |
author_sort | Tomita, Tatsuo |
collection | PubMed |
description | Aims/hypothesis: Protein gene product 9.5 (PGP 9.5) is a marker for neuroendocrine cells but has not been used for pancreatic islet cells and pancreatic endocrine tumors (PETs). Antibodies for PGP 9.5 are now commercially available for immunocytochemical study, with which immunostaining may be able to differentiate between benign and malignant PETs. Results: All 4 kinds of normal islet cells were positively immunostained for PGP 9.5—moderately positive for β-cells and strongly positive for δ-cells, whereas ganglion cells were immunostained more strongly than islet cells. Nine of 12 insulinomas were moderately to strongly positive for PGP 9.5. Two glucagonomas, 3 of 6 pancreatic polypeptidomas (PPomas), 3 of 9 gastrinomas, and 2 of 4 non-functioning PETs were negative for PGP 9.5. Materials and Methods: Thirty-four PETs were immunocytochemically stained for PGP 9.5 using a rabbit polyclonal antibody together with immunostaining for 4 pancreatic hormones, chromogranin A (CgA), and gastrin. PETs consisted of 12 insulinomas, 2 glucagonomas, 1 somatostatinoma (SRIFoma), 6 PPomas, 9 gastrinomas, and 4 non-functioning PETs. Conclusion/Interpretation: PGP 9.5 immunostaining was universally positive for 4 kinds of islet cells and was moderately to strongly positive for 9 of 12 (75%) insulinomas. All 22 non-β-cell PETs were negative or weakly positive for PGP 9.5, and thus negative or weakly positive PGP 9.5 immunostaining may be used as a marker for potential malignancy and poor prognosis for non-β-cell PETs. |
format | Online Article Text |
id | pubmed-4049838 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Landes Bioscience |
record_format | MEDLINE/PubMed |
spelling | pubmed-40498382014-06-18 PGP 9.5 immunocytochemical staining for pancreatic endocrine tumors Tomita, Tatsuo Islets Research Paper Aims/hypothesis: Protein gene product 9.5 (PGP 9.5) is a marker for neuroendocrine cells but has not been used for pancreatic islet cells and pancreatic endocrine tumors (PETs). Antibodies for PGP 9.5 are now commercially available for immunocytochemical study, with which immunostaining may be able to differentiate between benign and malignant PETs. Results: All 4 kinds of normal islet cells were positively immunostained for PGP 9.5—moderately positive for β-cells and strongly positive for δ-cells, whereas ganglion cells were immunostained more strongly than islet cells. Nine of 12 insulinomas were moderately to strongly positive for PGP 9.5. Two glucagonomas, 3 of 6 pancreatic polypeptidomas (PPomas), 3 of 9 gastrinomas, and 2 of 4 non-functioning PETs were negative for PGP 9.5. Materials and Methods: Thirty-four PETs were immunocytochemically stained for PGP 9.5 using a rabbit polyclonal antibody together with immunostaining for 4 pancreatic hormones, chromogranin A (CgA), and gastrin. PETs consisted of 12 insulinomas, 2 glucagonomas, 1 somatostatinoma (SRIFoma), 6 PPomas, 9 gastrinomas, and 4 non-functioning PETs. Conclusion/Interpretation: PGP 9.5 immunostaining was universally positive for 4 kinds of islet cells and was moderately to strongly positive for 9 of 12 (75%) insulinomas. All 22 non-β-cell PETs were negative or weakly positive for PGP 9.5, and thus negative or weakly positive PGP 9.5 immunostaining may be used as a marker for potential malignancy and poor prognosis for non-β-cell PETs. Landes Bioscience 2013-05-01 2013-06-27 /pmc/articles/PMC4049838/ /pubmed/23959334 http://dx.doi.org/10.4161/isl.25351 Text en Copyright © 2013 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited. |
spellingShingle | Research Paper Tomita, Tatsuo PGP 9.5 immunocytochemical staining for pancreatic endocrine tumors |
title | PGP 9.5 immunocytochemical staining for pancreatic endocrine tumors |
title_full | PGP 9.5 immunocytochemical staining for pancreatic endocrine tumors |
title_fullStr | PGP 9.5 immunocytochemical staining for pancreatic endocrine tumors |
title_full_unstemmed | PGP 9.5 immunocytochemical staining for pancreatic endocrine tumors |
title_short | PGP 9.5 immunocytochemical staining for pancreatic endocrine tumors |
title_sort | pgp 9.5 immunocytochemical staining for pancreatic endocrine tumors |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4049838/ https://www.ncbi.nlm.nih.gov/pubmed/23959334 http://dx.doi.org/10.4161/isl.25351 |
work_keys_str_mv | AT tomitatatsuo pgp95immunocytochemicalstainingforpancreaticendocrinetumors |