PSAT1, phosphoserine aminotransferase 1, 29968

N. diseases: 285; N. variants: 9
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.090 GeneticVariation phenotype BEFREE Within a median follow-up of 24.1 months, age (HR 1.03, 95% CI 1.01-1.06, p = 0.02), high PSA (1.55, 95% CI 1.07-2.25, p = 0.02) and low skeletal muscle volume (HR 1.61, 95% CI 1.10-2.35, p = 0.02) were the only independent prognostic factor for tumor progression. 31745255 2019
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.090 GeneticVariation phenotype BEFREE The secondary objectives are to estimate the diagnostic power of PSA-V and PSA-DT, to predict the risk of tumour progression. 30039385 2019
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.090 Biomarker phenotype BEFREE A growing amount of evidence has indicated that PSAT1 is an oncogene that plays an important role in cancer progression and metastasis. 29216929 2017
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.090 AlteredExpression phenotype BEFREE Overexpression of Phosphoserine Aminotransferase 1 (PSAT1) Predicts Poor Prognosis and Associates with Tumor Progression in Human Esophageal Squamous Cell Carcinoma. 27372650 2016
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.090 Biomarker phenotype BEFREE Genomic deletion of PTEN is associated with tumor progression and early PSA recurrence in ERG fusion-positive and fusion-negative prostate cancer. 22705054 2012
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.090 AlteredExpression phenotype BEFREE PSA recurrence in 76 patients who underwent radical prostatectomy and survival in 59 patients with metastases at diagnosis were analyzed to evaluate the influence of Mel-18 expression in cancer progression using Kaplan-Meier analysis and multivariate Cox regression analysis. 19395284 2011
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.090 Biomarker phenotype BEFREE PSA has been shown to down-regulate several proteins that are known to have involvement in tumor progression. 18646040 2008
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.090 Biomarker phenotype BEFREE Therefore, we confirm the therapeutic advantage of Serenoa repens over other 5alpha-reductase inhibitors as treatment with the phytotherapeutic agent will permit the continuous use of PSA measurements as a useful biomarker for prostate cancer screening and for evaluating tumour progression. 15543614 2005
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.090 AlteredExpression phenotype BEFREE The objectives of this study were to characterize the in vitro effects of sodium butyrate on human prostate cancer cell growth, PSA gene expression, and differentiation in the LNCaP tumor model and to determine whether tumor progression in vivo is delayed by isobutyramide, an orally bioavailable butyrate analogue with a longer half-life. 9581866 1998