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IDH1 Expression via the R132H Mutation–Specific Antibody in Adrenocortical Neoplasias—Prognostic Impact in Carcinomas

CONTEXT: Mutations to isocitrate dehydrogenase (IDH) appear to play a prognostic or predictive role in several neoplasias. Immunohistochemical staining designed to detect a specific R132H mutation to IDH1 showed expression in the normal adrenal cortex, raising interest to study the potential role of...

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Autores principales: Pennanen, Mirkka, Tynninen, Olli, Kytölä, Soili, Ellonen, Pekka, Mustonen, Harri, Heiskanen, Ilkka, Haglund, Caj, Arola, Johanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7069839/
https://www.ncbi.nlm.nih.gov/pubmed/32190803
http://dx.doi.org/10.1210/jendso/bvaa018
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author Pennanen, Mirkka
Tynninen, Olli
Kytölä, Soili
Ellonen, Pekka
Mustonen, Harri
Heiskanen, Ilkka
Haglund, Caj
Arola, Johanna
author_facet Pennanen, Mirkka
Tynninen, Olli
Kytölä, Soili
Ellonen, Pekka
Mustonen, Harri
Heiskanen, Ilkka
Haglund, Caj
Arola, Johanna
author_sort Pennanen, Mirkka
collection PubMed
description CONTEXT: Mutations to isocitrate dehydrogenase (IDH) appear to play a prognostic or predictive role in several neoplasias. Immunohistochemical staining designed to detect a specific R132H mutation to IDH1 showed expression in the normal adrenal cortex, raising interest to study the potential role of IDH1 in the pathogenesis of adrenocortical tumors. OBJECTIVE: The objective of this work is to study the role of IDH1 and its mutations in adrenocortical tumors. DESIGN AND PATIENTS: IDH1 R132H immunohistological staining was performed on a cohort of 197 adrenocortical tumors. The exon of the IDH1 gene was sequenced in 16 tumors. RESULTS: Positive IDH1 R132H immunohistochemical staining correlated with a better prognosis among patients with a malignant adrenocortical tumor. However, IDH1 R132H immunohistochemistry did not distinguish between local and metastasized tumors. We were unable to identify IDH1 mutations among our adrenocortical tumors using a targeted next-generation sequencing panel or via exon sequencing. CONCLUSIONS: Among adrenocortical carcinomas, IDH1 R132H immunopositivity correlated with a better prognosis. Thus, IDH1 R132H immunohistochemical staining could serve as a prognostic or as a potential predictive marker in adrenocortical carcinomas. Further research is needed to identify the possible alterations in IDH1 that could explain our findings, because we identified no known mutations to the IDH1 gene.
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spelling pubmed-70698392020-03-18 IDH1 Expression via the R132H Mutation–Specific Antibody in Adrenocortical Neoplasias—Prognostic Impact in Carcinomas Pennanen, Mirkka Tynninen, Olli Kytölä, Soili Ellonen, Pekka Mustonen, Harri Heiskanen, Ilkka Haglund, Caj Arola, Johanna J Endocr Soc Clinical Research Article CONTEXT: Mutations to isocitrate dehydrogenase (IDH) appear to play a prognostic or predictive role in several neoplasias. Immunohistochemical staining designed to detect a specific R132H mutation to IDH1 showed expression in the normal adrenal cortex, raising interest to study the potential role of IDH1 in the pathogenesis of adrenocortical tumors. OBJECTIVE: The objective of this work is to study the role of IDH1 and its mutations in adrenocortical tumors. DESIGN AND PATIENTS: IDH1 R132H immunohistological staining was performed on a cohort of 197 adrenocortical tumors. The exon of the IDH1 gene was sequenced in 16 tumors. RESULTS: Positive IDH1 R132H immunohistochemical staining correlated with a better prognosis among patients with a malignant adrenocortical tumor. However, IDH1 R132H immunohistochemistry did not distinguish between local and metastasized tumors. We were unable to identify IDH1 mutations among our adrenocortical tumors using a targeted next-generation sequencing panel or via exon sequencing. CONCLUSIONS: Among adrenocortical carcinomas, IDH1 R132H immunopositivity correlated with a better prognosis. Thus, IDH1 R132H immunohistochemical staining could serve as a prognostic or as a potential predictive marker in adrenocortical carcinomas. Further research is needed to identify the possible alterations in IDH1 that could explain our findings, because we identified no known mutations to the IDH1 gene. Oxford University Press 2020-02-18 /pmc/articles/PMC7069839/ /pubmed/32190803 http://dx.doi.org/10.1210/jendso/bvaa018 Text en © Endocrine Society 2020. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Clinical Research Article
Pennanen, Mirkka
Tynninen, Olli
Kytölä, Soili
Ellonen, Pekka
Mustonen, Harri
Heiskanen, Ilkka
Haglund, Caj
Arola, Johanna
IDH1 Expression via the R132H Mutation–Specific Antibody in Adrenocortical Neoplasias—Prognostic Impact in Carcinomas
title IDH1 Expression via the R132H Mutation–Specific Antibody in Adrenocortical Neoplasias—Prognostic Impact in Carcinomas
title_full IDH1 Expression via the R132H Mutation–Specific Antibody in Adrenocortical Neoplasias—Prognostic Impact in Carcinomas
title_fullStr IDH1 Expression via the R132H Mutation–Specific Antibody in Adrenocortical Neoplasias—Prognostic Impact in Carcinomas
title_full_unstemmed IDH1 Expression via the R132H Mutation–Specific Antibody in Adrenocortical Neoplasias—Prognostic Impact in Carcinomas
title_short IDH1 Expression via the R132H Mutation–Specific Antibody in Adrenocortical Neoplasias—Prognostic Impact in Carcinomas
title_sort idh1 expression via the r132h mutation–specific antibody in adrenocortical neoplasias—prognostic impact in carcinomas
topic Clinical Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7069839/
https://www.ncbi.nlm.nih.gov/pubmed/32190803
http://dx.doi.org/10.1210/jendso/bvaa018
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