Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Using an animal model, we show that reversion of PRKD1 promoter methylation with the DNA methyltransferase inhibitor decitabine restores PKD1 expression and blocks tumor spread and metastasis to the lung in a PKD1-dependent fashion.
|
23971832 |
2013 |
Hyperglycemia
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
Under a high-fat diet, deletion of PKD1 in β-cells worsened hyperglycemia, hyperinsulinemia, and glucose intolerance.
|
29038309 |
2018 |
Tuberous Sclerosis
|
0.030 |
Biomarker
|
disease |
BEFREE |
Two unrelated families in which TSC and PKD co-segregate were investigate.
|
9306341 |
1997 |
Adenocarcinoma of lung (disorder)
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
TP53 and PKD mutations were the two most frequently observed co-mutations in resected EGFR-mutated lung adenocarcinoma.
|
30820786 |
2019 |
Neoplasm Metastasis
|
0.080 |
Biomarker
|
phenotype |
BEFREE |
Together, our results suggest that PKD1 functions as a tumor and metastasis suppressor, at least partly by regulating Snail-mediated EMT, and that loss of PKD1 may contribute to acquisition of an aggressive malignant phenotype.
|
20940406 |
2010 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Together, our results suggest that PKD1 functions as a tumor and metastasis suppressor, at least partly by regulating Snail-mediated EMT, and that loss of PKD1 may contribute to acquisition of an aggressive malignant phenotype.
|
20940406 |
2010 |
Parkinson Disease
|
0.030 |
Biomarker
|
disease |
BEFREE |
Together, our findings demonstrate that quercetin activates the PKD1-Akt cell survival signaling axis and suggest that further exploration of quercetin as a promising neuroprotective agent for treating PD may offer clinical benefits.
|
28376279 |
2017 |
Polycystic Kidney Diseases
|
0.100 |
AlteredExpression
|
group |
BEFREE |
To overcome this problem, we previously demonstrated that folate-conjugated rapamycin (FC-rapa) targets polycystic kidneys due to the high expression of the folate receptor (FRα) and that treatment of a nonortholgous PKD mouse model leads to inhibition of renal cyst growth.
|
29717938 |
2018 |
Polycystic Kidney - body part
|
0.030 |
AlteredExpression
|
disease |
BEFREE |
To overcome this problem, we previously demonstrated that folate-conjugated rapamycin (FC-rapa) targets polycystic kidneys due to the high expression of the folate receptor (FRα) and that treatment of a nonortholgous PKD mouse model leads to inhibition of renal cyst growth.
|
29717938 |
2018 |
Autosomal Recessive Polycystic Kidney Disease
|
0.070 |
Biomarker
|
disease |
BEFREE |
To model PKD in human cells, we established induced pluripotent stem (iPS) cell lines from fibroblasts of three ADPKD and two ARPKD patients.
|
24009235 |
2013 |
Tumor Cell Invasion
|
0.100 |
AlteredExpression
|
phenotype |
BEFREE |
To further assess the role of PKD in bladder carcinoma, we examined the three PKD isoforms and found that PKD2 was highly expressed in eight bladder cancer cell lines and in urothelial carcinoma tissues from the TCGA database, and that short hairpin RNA (shRNA)-mediated knockdown of PKD2 dramatically reduced bladder cancer growth and invasion in vitro and in vivo, suggesting that the effect of the compound in bladder cancer is mediated through inhibition of PKD2.
|
29071385 |
2018 |
Malignant neoplasm of urinary bladder
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
To further assess the role of PKD in bladder carcinoma, we examined the three PKD isoforms and found that PKD2 was highly expressed in eight bladder cancer cell lines and in urothelial carcinoma tissues from the TCGA database, and that short hairpin RNA (shRNA)-mediated knockdown of PKD2 dramatically reduced bladder cancer growth and invasion in vitro and in vivo, suggesting that the effect of the compound in bladder cancer is mediated through inhibition of PKD2.
|
29071385 |
2018 |
Bladder Neoplasm
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
To further assess the role of PKD in bladder carcinoma, we examined the three PKD isoforms and found that PKD2 was highly expressed in eight bladder cancer cell lines and in urothelial carcinoma tissues from the TCGA database, and that short hairpin RNA (shRNA)-mediated knockdown of PKD2 dramatically reduced bladder cancer growth and invasion in vitro and in vivo, suggesting that the effect of the compound in bladder cancer is mediated through inhibition of PKD2.
|
29071385 |
2018 |
Carcinoma of bladder
|
0.010 |
Biomarker
|
disease |
BEFREE |
To further assess the role of PKD in bladder carcinoma, we examined the three PKD isoforms and found that PKD2 was highly expressed in eight bladder cancer cell lines and in urothelial carcinoma tissues from the TCGA database, and that short hairpin RNA (shRNA)-mediated knockdown of PKD2 dramatically reduced bladder cancer growth and invasion in vitro and in vivo, suggesting that the effect of the compound in bladder cancer is mediated through inhibition of PKD2.
|
29071385 |
2018 |
Polycystic Kidney, Autosomal Dominant
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
To determine the interrelationship of seminal megavesicles (seminal vesicles with lumen diameter > 10mm) and prostatic cysts in ADPKD and to determine whether there are associations with PKD gene mutations.
|
30230107 |
2019 |
Autosomal Recessive Polycystic Kidney Disease
|
0.070 |
GeneticVariation
|
disease |
BEFREE |
To assess the frequency of additional variations in PKD1, PKD2, HNF1B, and PKHD1 associated with the familial PKD mutation in early ADPKD, these four genes were screened in 42 patients with early ADPKD in 41 families.
|
26139440 |
2016 |
Chronic kidney disease stage 3
|
0.020 |
GeneticVariation
|
disease |
BEFREE |
Time to hypertension treatment, stage 3 chronic kidney disease (CKD), ESRD, and death was measured, and the impact of genotype, gender, gender of parent who transmitted PKD, family, family history of essential hypertension, parity, and oral contraceptive pill was assessed.
|
17699277 |
2006 |
Hypertensive disease
|
0.040 |
GeneticVariation
|
group |
BEFREE |
Time to hypertension treatment, stage 3 chronic kidney disease (CKD), ESRD, and death was measured, and the impact of genotype, gender, gender of parent who transmitted PKD, family, family history of essential hypertension, parity, and oral contraceptive pill was assessed.
|
17699277 |
2006 |
Obesity
|
0.010 |
Biomarker
|
disease |
BEFREE |
Thus, depletion of PKD1 in adipocytes increases energy dissipation by several complementary mechanisms and might represent an attractive strategy to treat obesity and its related complications.
|
30389661 |
2018 |
Involuntary Movements
|
0.010 |
Biomarker
|
phenotype |
BEFREE |
Thus, PKD and BFIC2 are genetically identical and may cause convulsions and involuntary movements via a similar mechanism.
|
22399141 |
2012 |
Seizures
|
0.010 |
Biomarker
|
phenotype |
BEFREE |
Thus, PKD and BFIC2 are genetically identical and may cause convulsions and involuntary movements via a similar mechanism.
|
22399141 |
2012 |
Convulsions
|
0.010 |
Biomarker
|
phenotype |
BEFREE |
Thus, PKD and BFIC2 are genetically identical and may cause convulsions and involuntary movements via a similar mechanism.
|
22399141 |
2012 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
This study suggests that PKD1 may be a potential target for microenvironment-directed tumor biotherapy.
|
29901206 |
2018 |
Carcinogenesis
|
0.040 |
Biomarker
|
phenotype |
BEFREE |
This study suggests a novel role of PKD1 as a key modulator of the glucose metabolism in PanCa cells accelerating tumorigenesis and chemo-resistance.
|
31819177 |
2020 |
Polycystic Kidney, Autosomal Dominant
|
0.100 |
AlteredExpression
|
disease |
BEFREE |
This study not only provides one of the mechanisms of how c-Myc is upregulated in PKD but also suggests that targeting Brd4 with JQ1 may function as a novel epigenetic approach in ADPKD.
|
25877301 |
2015 |