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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...

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Autor principal: Tomita, Tatsuo
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
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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.
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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
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