Background: GA-binding protein A (GABPA), a transcription factor, is broadly involved in physiological and pathological processes. Several studies have investigated the relationship between GABPA expression level and outcomes of various malignancies. However, the function and clinicopathological significance of GABPA in endometrial carcinoma (EC) remain obscure.
Methods: The GABPA mRNA expression in EC tissues and adjacent nonneoplastic tissues in the TCGA database was involved in our study. The protein expression of GABPA in 107 EC tissues and 15 normal endometrial tissues was detected by immunohistochemistry.
Results: The GABPA expression was significantly downregulated in EC tissues compared with its expression in normal tissues ( < 0.001). The expression of GABPA was markedly correlated with type II EC ( < 0.01) and grade 3 EC ( < 0.05). A tendency has been observed that patients with low GABPA levels had relatively poorer overall survival (OS) ( = 0.036) and disease-free survival (DFS) ( = 0.016) than patients with high GABPA levels. The multivariate Cox proportional hazard model showed that lower expression of GABPA was an independent poor prognostic factor for OS ( = 0.043) and DFS ( = 0.045). Similar correlation between low expression levels of GABPA and unfavorable prognosis has also been found in type II or grade 3 EC. IHC analysis showed EC tissues had low expression of GABPA, which indicated relatively poor prognosis. Moreover, we identified that the GABPA mRNA expression was negatively correlated with its methylation level ( = -0.2512, < 0.001) which is one of the mechanisms for the silencing of GABPA gene.
Conclusion: GABPA may act as an independent predictor of clinical prognosis and serve as a potential target gene for EC therapy.
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http://dx.doi.org/10.1155/2021/5552614 | DOI Listing |
iScience
December 2024
The First Clinical Medical College of Lanzhou University, Lanzhou 730000, China.
Despite decades of research, the pathogenesis of endometriosis remains unclear. Recent studies have shown that microRNAs play an important role in this condition. In this study, we found that the expression level of miR-450b-5p was increased in ectopic endometrial tissues and that GA-binding protein A (GABPA) and HOXD10 expression levels were decreased.
View Article and Find Full Text PDFNat Cell Biol
January 2025
Howard Hughes Medical Institute, Boston Children's Hospital, Boston, MA, USA.
The establishment of naive pluripotency is a continuous process starting with the generation of inner cell mass (ICM) that then differentiates into epiblast (EPI). Recent studies have revealed key transcription factors (TFs) for ICM formation, but which TFs initiate EPI specification remains unknown. Here, using a targeted rapid protein degradation system, we show that GABPA is not only a regulator of major ZGA, but also a master EPI specifier required for naive pluripotency establishment by regulating 47% of EPI genes during E3.
View Article and Find Full Text PDFbioRxiv
November 2024
Howard Hughes Medical Institute, Boston Children's Hospital, Boston, MA 02115, USA.
The establishment of naïve pluripotency is a continuous process starting with the generation of inner cell mass (ICM) which then differentiating into epiblast (EPI). Recent studies have revealed key transcription factors (TFs) for ICM formation, but which TFs initiate EPI specification remains unknown. Here, using a targeted rapid protein degradation system, we show that GABPA is not only a regulator of major ZGA, but also a master EPI specifier required for naïve pluripotency establishment by regulating 47% of EPI genes during E3.
View Article and Find Full Text PDFSci Rep
November 2024
Department of Urology, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200080, People's Republic of China.
Clear cell renal cell carcinoma (ccRCC) is a common genitourinary malignancy characterized by dysregulated cellular metabolism leading to aberrant glucose metabolism, fatty acid accumulation, and excessive reactive oxygen species production. ccRCC cells exhibit an augmented oxidative stress response. Complex interactions between iron metabolism and lipid homeostasis in ccRCC cells require a counteracting response that enables ferroptosis evasion and survival maintenance.
View Article and Find Full Text PDFRedox Biol
November 2024
Department of Urology, Institute of Urology, Sichuan Clinical Research Center for Urological and Kidney Diseases, West China Hospital, Sichuan University, Chengdu, China. Electronic address:
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