PLCL1, phospholipase C like 1 (inactive), 5334

N. diseases: 69; N. variants: 96
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus
0.030 GeneticVariation disease BEFREE A single-nucleotide polymorphism (rs2274223: A5780G:His1927Arg) in the phospholipase C epsilon gene (PLCϵ) was recently identified as a susceptibility locus for esophageal cancer in Chinese subjects. 23390063 2013
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus
0.030 GeneticVariation disease BEFREE Multiple studies with large clinic-based cohorts revealed that variations of the phospholipase C epsilon (PLCE1) gene were associated with esophageal cancer susceptibility. 28147304 2017
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus
0.030 AlteredExpression disease BEFREE To investigate the effect and mechanism of phospholipase C epsilon gene 1 (<i>PLCE1</i>) expression on esophageal cancer cell lines. 30450849 2018
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.030 AlteredExpression disease BEFREE MATERIAL AND METHODS We assessed PLCε and PTEN expression in human benign prostate tissues compared to prostate cancer tissues by immunohistochemistry. 29330357 2018
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.030 Biomarker disease BEFREE Our findings suggest that PLCε is a putative oncogene and prognostic marker, potentially representing a novel therapeutic target for PCa. 25796442 2015
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.030 Biomarker disease BEFREE It was found that the PLCε expression was excessively upregulated in the majority of CRPC tissues, and PLCε positivity was linked to poor progression‑free survival (PFS) and overall survival (OS) in patients with PCa. 30864728 2019
CUI: C0699885
Disease: Carcinoma of bladder
Carcinoma of bladder
0.030 Biomarker disease BEFREE The knockdown of PLCε by shRNA could inhibit bladder tumor growth and might be an alternative approach for human bladder cancer therapy. 21705050 2011
CUI: C0699885
Disease: Carcinoma of bladder
Carcinoma of bladder
0.030 Biomarker disease BEFREE Collectively, the present study demonstrated that PLCε may regulate glycolysis through the STAT3/LDHA pathway to take part in the development of human UBC. 30864733 2019
CUI: C0699885
Disease: Carcinoma of bladder
Carcinoma of bladder
0.030 Biomarker disease BEFREE Knockdown of phospholipase C-epsilon by short-hairpin RNA-mediated gene silencing induces apoptosis in human bladder cancer cell lines. 23484808 2013
CUI: C0005695
Disease: Bladder Neoplasm
Bladder Neoplasm
0.020 Biomarker disease BEFREE Knockdown of phospholipase C-epsilon by short-hairpin RNA-mediated gene silencing induces apoptosis in human bladder cancer cell lines. 23484808 2013
CUI: C0005695
Disease: Bladder Neoplasm
Bladder Neoplasm
0.020 Biomarker disease BEFREE The knockdown of PLCε by shRNA could inhibit bladder tumor growth and might be an alternative approach for human bladder cancer therapy. 21705050 2011
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.020 GeneticVariation disease BEFREE Association between phospholipase C epsilon gene (PLCE1) polymorphism and colorectal cancer risk in a Chinese population. 24496148 2014
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.020 Biomarker disease BEFREE Phospholipase C epsilon plays a suppressive role in incidence of colorectal cancer. 21667163 2012
Malignant neoplasm of colon and/or rectum
0.020 Biomarker disease BEFREE Phospholipase C epsilon plays a suppressive role in incidence of colorectal cancer. 21667163 2012
Malignant neoplasm of colon and/or rectum
0.020 GeneticVariation disease BEFREE Association between phospholipase C epsilon gene (PLCE1) polymorphism and colorectal cancer risk in a Chinese population. 24496148 2014
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.010 GeneticVariation disease BEFREE Thus these APP and PRIP mutations are rare in both FAD and nonfamilial AD. 1679288 1991
CUI: C0003123
Disease: Anorexia
Anorexia
0.010 Biomarker disease BEFREE PRIP gene (Prip1 and Prip2) knockout (Prip-KO) mice intraperitoneally (ip) administered with LPS exhibited increased anorexia responses compared with wild-type (WT) controls. 31589911 2019
CUI: C0003504
Disease: Aortic Valve Insufficiency
Aortic Valve Insufficiency
0.010 Biomarker disease BEFREE Additionally, we demonstrate that the activation of both the Notch and AR signalling pathways is involved in PLCε-mediated oncogenic effects in PCa. 25796442 2015
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma
0.010 Biomarker disease BEFREE Taken together, these findings suggest that PLCε promotes RCC cell growth via NF-κB-mediated upregulation of VEGF. 24510280 2014
CUI: C0011633
Disease: Dermatomyositis
Dermatomyositis
0.010 GeneticVariation disease BEFREE Recently, phospholipase C-like 1 (PLCL1) has been identified as a potential genetic susceptibility locus for dermatomyositis (DM) in patients of European ancestry. 26603167 2016
CUI: C0014868
Disease: Esophagitis
Esophagitis
0.010 GeneticVariation disease BEFREE A sequence variant in the phospholipase C epsilon C2 domain is associated with esophageal carcinoma and esophagitis. 23390063 2013
Gerstmann-Straussler-Scheinker Disease
0.010 GeneticVariation disease BEFREE We also tested for the APP codon 693 mutation associated with hereditary cerebral hemorrhage with amyloidosis-Dutch type, for PRIP gene missense mutations at codons 102, 117, and 200, and for the PRIP insertion mutations which are associated with Creutzfeld-Jakob disease and Gerstmann-Straussler Scheinker syndrome. 1679288 1991
CUI: C0017638
Disease: Glioma
Glioma
0.010 AlteredExpression disease BEFREE In the present study, the expression of PLCε and glioma‑associated homolog (Gli)‑1/Gli‑2 in benign prostatic hyperplasia (BPH), PCa and CRPC tissues and cells was investigated, and the correlations between PLCε and Gli‑1/Gli‑2 in CRPC tissues and cell lines were further explored. 30864728 2019
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic
0.010 GeneticVariation disease BEFREE Using positional cloning, we identified mutations in the phospholipase C epsilon gene (PLCE1) as causing early-onset nephrotic syndrome with end-stage kidney disease. 17086182 2006
CUI: C0029463
Disease: Osteosarcoma
Osteosarcoma
0.010 AlteredExpression disease BEFREE Silencing of phosphoinositide-specific phospholipase C ε remodulates the expression of the phosphoinositide signal transduction pathway in human osteosarcoma cell lines. 25075031 2014