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Association of PTTG1 expression with invasiveness of non-functioning pituitary adenomas
BACKGROUND: Pituitary tumor transforming gene 1 (PTTG1), paired-like homeodomain 2 (PITX2), and galectin-3 have been widely studied as predictive biomarkers for various tumors and are involved in tumorigenesis and tumor progression. We evaluated the usefulness of PTTG1, PITX2, and galectin-3 as pred...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Society of Pathologists/The Korean Society for Cytopathology
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8743807/ https://www.ncbi.nlm.nih.gov/pubmed/34645111 http://dx.doi.org/10.4132/jptm.2021.08.31 |
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author | Kum, Su Jung Lee, Hye Won Kim, Soon Gu Park, Hyungsik Hwang, Ilseon Kim, Sang Pyo |
author_facet | Kum, Su Jung Lee, Hye Won Kim, Soon Gu Park, Hyungsik Hwang, Ilseon Kim, Sang Pyo |
author_sort | Kum, Su Jung |
collection | PubMed |
description | BACKGROUND: Pituitary tumor transforming gene 1 (PTTG1), paired-like homeodomain 2 (PITX2), and galectin-3 have been widely studied as predictive biomarkers for various tumors and are involved in tumorigenesis and tumor progression. We evaluated the usefulness of PTTG1, PITX2, and galectin-3 as predictive biomarkers for invasive non-functioning pituitary adenomas (NFPAs) by determining the relationship between the expressions of these three proteins and the invasiveness of the NFPAs. We also investigated whether PTTG1, E-cadherin, and Ki-67, which are known to be related to each other, show a correlation with NFPA features. METHODS: A retrospective study was conducted on 87 patients with NPFAs who underwent surgical removal. The NFPAs were classified into three groups based on magnetic resonance imaging findings of suprasellar extension and cavernous sinus invasion. Immunohistochemical staining for PTTG1, PITX2, galectin-3, E-cadherin, and Ki-67 was performed on tissue microarrays. RESULTS: PTTG1 expression showed a statistically significant correlation with the invasiveness of NFPAs, whereas PITX2 and galectin-3 did not have a relationship with the invasiveness of NFPAs. Moreover, there was no association among PTTG1, E-cadherin, and Ki-67 expression. CONCLUSIONS: PTTG1 has the potential to serve as a predictive biomarker for invasive NFPA. Furthermore, this study may serve as a reference for the development of PTTG1-targeted therapeutic agents. |
format | Online Article Text |
id | pubmed-8743807 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Korean Society of Pathologists/The Korean Society for Cytopathology |
record_format | MEDLINE/PubMed |
spelling | pubmed-87438072022-01-18 Association of PTTG1 expression with invasiveness of non-functioning pituitary adenomas Kum, Su Jung Lee, Hye Won Kim, Soon Gu Park, Hyungsik Hwang, Ilseon Kim, Sang Pyo J Pathol Transl Med Original Article BACKGROUND: Pituitary tumor transforming gene 1 (PTTG1), paired-like homeodomain 2 (PITX2), and galectin-3 have been widely studied as predictive biomarkers for various tumors and are involved in tumorigenesis and tumor progression. We evaluated the usefulness of PTTG1, PITX2, and galectin-3 as predictive biomarkers for invasive non-functioning pituitary adenomas (NFPAs) by determining the relationship between the expressions of these three proteins and the invasiveness of the NFPAs. We also investigated whether PTTG1, E-cadherin, and Ki-67, which are known to be related to each other, show a correlation with NFPA features. METHODS: A retrospective study was conducted on 87 patients with NPFAs who underwent surgical removal. The NFPAs were classified into three groups based on magnetic resonance imaging findings of suprasellar extension and cavernous sinus invasion. Immunohistochemical staining for PTTG1, PITX2, galectin-3, E-cadherin, and Ki-67 was performed on tissue microarrays. RESULTS: PTTG1 expression showed a statistically significant correlation with the invasiveness of NFPAs, whereas PITX2 and galectin-3 did not have a relationship with the invasiveness of NFPAs. Moreover, there was no association among PTTG1, E-cadherin, and Ki-67 expression. CONCLUSIONS: PTTG1 has the potential to serve as a predictive biomarker for invasive NFPA. Furthermore, this study may serve as a reference for the development of PTTG1-targeted therapeutic agents. The Korean Society of Pathologists/The Korean Society for Cytopathology 2022-01 2021-10-15 /pmc/articles/PMC8743807/ /pubmed/34645111 http://dx.doi.org/10.4132/jptm.2021.08.31 Text en © 2022 The Korean Society of Pathologists/The Korean Society for Cytopathology https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Kum, Su Jung Lee, Hye Won Kim, Soon Gu Park, Hyungsik Hwang, Ilseon Kim, Sang Pyo Association of PTTG1 expression with invasiveness of non-functioning pituitary adenomas |
title | Association of PTTG1 expression with invasiveness of non-functioning pituitary adenomas |
title_full | Association of PTTG1 expression with invasiveness of non-functioning pituitary adenomas |
title_fullStr | Association of PTTG1 expression with invasiveness of non-functioning pituitary adenomas |
title_full_unstemmed | Association of PTTG1 expression with invasiveness of non-functioning pituitary adenomas |
title_short | Association of PTTG1 expression with invasiveness of non-functioning pituitary adenomas |
title_sort | association of pttg1 expression with invasiveness of non-functioning pituitary adenomas |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8743807/ https://www.ncbi.nlm.nih.gov/pubmed/34645111 http://dx.doi.org/10.4132/jptm.2021.08.31 |
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