3.8 Article

Association of PTTG1 expression with invasiveness of non-functioning pituitary adenomas

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KOREAN SOC PATHOLOGISTS
DOI: 10.4132/jptm.2021.08.31

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Non-functioning pituitary adenomas; Pituitary tumor transforming gene expression; Invasiveness

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  1. Institute for Cancer Reseach Keimyung University Dongsan Medical Center

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The study found that PTTG1 expression is significantly correlated with the invasiveness of NFPAs, while PITX2 and galectin-3 do not have a relationship with invasiveness. Additionally, there was no association among PTTG1, E-cadherin, and Ki-67 expression.
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 stain-ing 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 in-vasiveness 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.

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