GSTP1, glutathione S-transferase pi 1, 2950

N. diseases: 610; N. variants: 18
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0001206
Disease: Acromegaly
Acromegaly
0.010 GeneticVariation disease BEFREE In this study, we assessed the contribution of GSTP1 gene promoter methylation status, per se or in combination with the occurrence of the AHR gene rs2066853 variant, on clinical features and response to somatostatin analogs (SSA) treatment in acromegaly patients. 30488289 2019
CUI: C0004936
Disease: Mental disorders
Mental disorders
0.010 Biomarker group BEFREE The involvement of GSTP in the oxidative stress and in other human pathologies like cancer, liver and neurodegenerative diseases, and psychiatric disorders is also reported. 31357662 2019
CUI: C0009375
Disease: Colonic Neoplasms
Colonic Neoplasms
0.010 Biomarker group BEFREE We investigated the immunohistochemical staining characteristics of cytochrome P450 1A1 (CYP1A1), CYPB1, CYP2E1, and glutathione S-transferase P1 (GSTP1), GSTT1, GSTO1, GSTK1 in colon tumor and surrounding normal colon tissues. 30092668 2019
CUI: C0009376
Disease: Colonic Polyps
Colonic Polyps
0.010 Biomarker phenotype BEFREE GSTP1-methyl patients showed a higher prevalence of diabetes mellitus (p = 0.01), colonic polyps (p = 0.05), and were more resistant to SSA (p = 0.02) as compared to GSTP1 unmethylated patients (GSTP1-unmethyl). 30488289 2019
CUI: C0011168
Disease: Deglutition Disorders
Deglutition Disorders
0.010 GeneticVariation group BEFREE In addition, the presence of G allele of GSTP1 was associated with a significantly lower risk of severe dysphagia (P = .0004). 30973677 2019
CUI: C0027497
Disease: Nausea
Nausea
0.010 GeneticVariation phenotype BEFREE GSTP1 c.313A>G genotyping may reduce the use of preventive support for chemotherapy induced nausea and lower the overall cost of treatment. 30870506 2019
CUI: C0153594
Disease: Malignant neoplasm of testis
Malignant neoplasm of testis
0.010 GeneticVariation disease BEFREE CYP1A1*2C, GSTM1null, GSTT1null, and GSTP1 (rs1695) are statistically related to the risk of appearance of TCa, alone or associated with nongenetic factors. 31107374 2019
CUI: C0205700
Disease: Asymmetric Septal Hypertrophy
Asymmetric Septal Hypertrophy
0.010 Biomarker disease BEFREE The different expression of tumor suppressors, RASSF1A, RUNX3, and GSTP1, in patients with alcoholic steatohepatitis (ASH) vs non-alcoholic steatohepatitis (NASH). 30951700 2019
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
0.010 Biomarker phenotype BEFREE The involvement of GSTP in the oxidative stress and in other human pathologies like cancer, liver and neurodegenerative diseases, and psychiatric disorders is also reported. 31357662 2019
CUI: C0524851
Disease: Neurodegenerative Disorders
Neurodegenerative Disorders
0.010 Biomarker group BEFREE The involvement of GSTP in the oxidative stress and in other human pathologies like cancer, liver and neurodegenerative diseases, and psychiatric disorders is also reported. 31357662 2019
Malignant neoplasm of gastrointestinal tract
0.010 AlteredExpression disease BEFREE <b>Methods</b>: A meta-analysis about <i>GSTP1</i>, <i>GSTM1</i> and <i>GSTT1</i> variants and the GSTP1 expression level on chemotherapy efficacy of GIC patients was performed using data from PubMed, PMC, EMBASE, Web of Science, and Wanfang database. 31281468 2019
Malignant Testicular Germ Cell Tumor
0.010 GeneticVariation disease BEFREE CYP1A1*2C, GSTM1null, GSTT1null, and GSTP1 (rs1695) are statistically related to the risk of appearance of TCa, alone or associated with nongenetic factors. 31107374 2019
CUI: C0948441
Disease: Venoocclusive disease
Venoocclusive disease
0.010 Biomarker group BEFREE GSTA1, GSTM1 and GSTP1 were not significantly associated with VOD occurrence. 30511436 2019
CUI: C1510472
Disease: Drug Dependence
Drug Dependence
0.010 GeneticVariation group BEFREE Relationship between glutathione S-transferase P1 (GSTP1, OMIM: 134660) variants and the risk of drug dependency is unknown. 30121884 2019
CUI: C1527390
Disease: Neoplasms, Intracranial
Neoplasms, Intracranial
0.010 AlteredExpression group BEFREE GSTP1 and CYP expression is increased in intracranial tumors. 30321868 2019
CUI: C1608408
Disease: Malignant transformation
Malignant transformation
0.010 AlteredExpression phenotype BEFREE Our results revealed a novel potential mechanism of HDV-induced liver injury and hepatocarcinogenesis: s-HDAg can inhibit GSTP1 expression by directly binding to GSTP1 mRNA, which leads to accumulation of cellular ROS, resulting in high cellular apoptotic ratios and increased selective pressure for malignant transformation. 30153423 2019
CUI: C2718067
Disease: Alcoholic Steatohepatitis
Alcoholic Steatohepatitis
0.010 Biomarker disease BEFREE The different expression of tumor suppressors, RASSF1A, RUNX3, and GSTP1, in patients with alcoholic steatohepatitis (ASH) vs non-alcoholic steatohepatitis (NASH). 30951700 2019
CUI: C2732618
Disease: Sessile Serrated Adenoma/Polyp
Sessile Serrated Adenoma/Polyp
0.010 GeneticVariation disease BEFREE In this study, we assessed the contribution of GSTP1 gene promoter methylation status, per se or in combination with the occurrence of the AHR gene rs2066853 variant, on clinical features and response to somatostatin analogs (SSA) treatment in acromegaly patients. 30488289 2019
CUI: C4329280
Disease: Advanced Head and Neck Carcinoma
Advanced Head and Neck Carcinoma
0.010 GeneticVariation disease BEFREE Association of GSTP1 and ERCC1 polymorphisms with toxicity in locally advanced head and neck cancer platinum-based chemoradiotherapy treatment. 30973677 2019
CUI: C4529962
Disease: Fatty Liver Disease
Fatty Liver Disease
0.010 Biomarker disease BEFREE The different expression of tumor suppressors, RASSF1A, RUNX3, and GSTP1, in patients with alcoholic steatohepatitis (ASH) vs non-alcoholic steatohepatitis (NASH). 30951700 2019
CUI: C0001824
Disease: Agranulocytosis
Agranulocytosis
0.010 GeneticVariation disease BEFREE GSTP1 rs1695 gene polymorphism showed a significant correlation with granulocytopenia induced by platinum-based drugs (dominant genetic model: OR=1.60, 95% CI=1.19. 30238837 2018
CUI: C0013238
Disease: Dry Eye Syndromes
Dry Eye Syndromes
0.010 AlteredExpression disease BEFREE Analysis of differential protein expression between study groups: We observed increased expression of proteins S100A4, S100A8, retinal dehydrogenase-1, peroxiredoxin-1, annexin-A1, annexin-A2, α-enolase, and glutathione S-transferase-P in DE, whereas the highest expression of peroxiredoxin-6, actin cytoplasmic-1, peroxiredoxin-2, and heat shock protein HSP-90-α was observed in MGD; ii). 28336260 2018
CUI: C0017154
Disease: Gastritis, Atrophic
Gastritis, Atrophic
0.010 GeneticVariation disease BEFREE Two pairwise combinations (<i>ERCC5</i> rs2094258 and rs873601 with <i>GSTP1</i> rs1695) influenced AG risk (<i>P</i><sub>interaction</sub> = 0.008 and 0.043, respectively), and the ERCC5 rs2094258-GSTP1 rs1695 SNP pair demonstrated an antagonistic effect, while <i>ERCC5</i> rs873601-<i>GSTP1</i> rs1695 showed a synergistic effect on AG risk OR = 0.51 and 1.79, respectively). 29434449 2018
CUI: C0027831
Disease: Neurofibromatosis 1
Neurofibromatosis 1
0.010 Biomarker disease BEFREE On the other hand, SWCNT exposure showed hypermethylation on functionally important genes, such as SKI proto-oncogene (SKI), glutathione S-transferase pi 1 (GTSP1) and shroom family member 2 (SHROOM2) and neurofibromatosis type I (NF1), which the latter is both hypermethylated and downregulated. 29426343 2018
CUI: C0035455
Disease: Rhinitis
Rhinitis
0.010 GeneticVariation disease BEFREE To evaluate whether polymorphisms of IL4R (rs1805015), IL13 (rs20541), IL17A (rs2275913) and GSTP1 (rs1695) genes are associated with rhinitis and/or asthma in adults of Portuguese ancestry. 27561723 2018