Pancreatic carcinoma
|
0.700 |
Biomarker
|
disease |
BEFREE |
In this study, we investigated the relationship between SRPK2, Numb and p53 in the development of pancreatic cancer with or without chemical agent treatment in vitro.
|
30724469 |
2019 |
Pancreatic carcinoma
|
0.700 |
GeneticVariation
|
disease |
BEFREE |
Potential functional variants in SMC2 and TP53 in the AURORA pathway genes and risk of pancreatic cancer.
|
30794721 |
2019 |
Pancreatic carcinoma
|
0.700 |
Biomarker
|
disease |
BEFREE |
Hypoxia-induced feedback of HIF-1α and lncRNA-CF129 contributes to pancreatic cancer progression through stabilization of p53 protein.
|
31367258 |
2019 |
Pancreatic carcinoma
|
0.700 |
Biomarker
|
disease |
BEFREE |
RESULTS The most important biotargets for plumbagin in PC were identified as TP53, MAPK1, BCL2, and IL6.
|
31230062 |
2019 |
Pancreatic carcinoma
|
0.700 |
GeneticVariation
|
disease |
BEFREE |
We found that six novel tagging single-nucleotide polymorphisms (SNPs) (i.e, MAP2 rs35075084 T > deletion, PRKAG2 rs2727572 C > T and rs34852782 A > deletion, TP53 rs9895829 A > G, and RPTOR rs62068300 G > A and rs3751936 G > C) were significantly associated with an increased PanC risk.
|
30997723 |
2019 |
Pancreatic carcinoma
|
0.700 |
Biomarker
|
disease |
BEFREE |
The KPC mouse model, driven by the Kras and Trp53 transgenes, is well regarded for faithful recapitulation of human pancreatic cancer biology.
|
31780749 |
2019 |
Pancreatic carcinoma
|
0.700 |
Biomarker
|
disease |
BEFREE |
Dietary Garcinol Arrests Pancreatic Cancer in p53 and K-ras Conditional Mutant Mouse Model.
|
30273070 |
2018 |
Pancreatic carcinoma
|
0.700 |
GeneticVariation
|
disease |
BEFREE |
Together, this study highlights the therapeutic potential of NL in mutant p53 expressing pancreatic cancer.
|
29107110 |
2018 |
Pancreatic carcinoma
|
0.700 |
GeneticVariation
|
disease |
BEFREE |
Accumulating evidence strongly suggests that p53 mutations contribute to the acquisition and/or maintenance of drug-resistant property of pancreatic cancer.
|
29558908 |
2018 |
Pancreatic carcinoma
|
0.700 |
AlteredExpression
|
disease |
BEFREE |
In this study, we demonstrate that inactivation of Cdkn2b (p15ink4b) is necessary for induction of pancreatic cancer by oncogenic KRAS<sup>G12D</sup> expression and inactivation of Tp53 and Cdkn2a in adult mouse pancreatic ductal cells (P60 or older).
|
28892048 |
2018 |
Pancreatic carcinoma
|
0.700 |
GeneticVariation
|
disease |
BEFREE |
In summary, our observations strongly indicated that, similarly to 2D monolayer culture, RUNX2 gene silencing increased GEM sensitivity of MiaPaCa‑2 spheres and highlighted the therapeutic potential of RUNX2 in pancreatic cancer with p53 mutation.
|
29620279 |
2018 |
Pancreatic carcinoma
|
0.700 |
GeneticVariation
|
disease |
BEFREE |
Comparing 3030 case patients with pancreatic cancer (43.2% female; 95.6% non-Hispanic white; mean age at diagnosis, 65.3 [SD, 10.7] years) with reference controls, significant associations were observed between pancreatic cancer and mutations in CDKN2A (0.3% of cases and 0.02% of controls; odds ratio [OR], 12.33; 95% CI, 5.43-25.61); TP53 (0.2% of cases and 0.02% of controls; OR, 6.70; 95% CI, 2.52-14.95); MLH1 (0.13% of cases and 0.02% of controls; OR, 6.66; 95% CI, 1.94-17.53); BRCA2 (1.9% of cases and 0.3% of controls; OR, 6.20; 95% CI, 4.62-8.17); ATM (2.3% of cases and 0.37% of controls; OR, 5.71; 95% CI, 4.38-7.33); and BRCA1 (0.6% of cases and 0.2% of controls; OR, 2.58; 95% CI, 1.54-4.05).
|
29922827 |
2018 |
Pancreatic carcinoma
|
0.700 |
GeneticVariation
|
disease |
BEFREE |
Our work establishes a requirement for mutant p53 for the formation and maintenance of pancreatic cancer precursor lesions.
|
29367463 |
2018 |
Pancreatic carcinoma
|
0.700 |
GeneticVariation
|
disease |
BEFREE |
Detection of KRAS or p53 mutation in plasma is not an effective screening tool for pancreatic cancer because accumulation of multiple mutations is required for malignant transformation in the pancreas.
|
29303908 |
2018 |
Pancreatic carcinoma
|
0.700 |
GeneticVariation
|
disease |
BEFREE |
K-ras<sup>LSL-G12D/+</sup>:: p53<sup>LSL-R172H/+</sup>:: Pdx-1-Cre (KPC) mice are an established model of pancreatic cancer that specifically express mutants of both K-ras and p53 in the pancreas by using Pdx-1-Cre.
|
28971839 |
2018 |
Pancreatic carcinoma
|
0.700 |
GeneticVariation
|
disease |
BEFREE |
Detection of mutant KRAS and TP53 DNA in circulating exosomes from healthy individuals and patients with pancreatic cancer.
|
28121262 |
2017 |
Pancreatic carcinoma
|
0.700 |
Biomarker
|
disease |
BEFREE |
Thus, we investigate the relationship among MSI2, Numb, MDM2, and p53 in PC <i>in vitro</i> and <i>in</i><i>vivo</i>, an association that has not been reported to our knowledge.
|
28223335 |
2017 |
Pancreatic carcinoma
|
0.700 |
GeneticVariation
|
disease |
BEFREE |
Mutant p53 Together with TGFβ Signaling Influence Organ-Specific Hematogenous Colonization Patterns of Pancreatic Cancer.
|
27637888 |
2017 |
Pancreatic carcinoma
|
0.700 |
GeneticVariation
|
disease |
BEFREE |
Based on these findings, trichodermin is a potential therapeutic agent worthy of further development into a clinical trial candidate for treating cancer, especially the mutant p53 pancreatic cancer.
|
27965041 |
2017 |
Pancreatic carcinoma
|
0.700 |
GeneticVariation
|
disease |
BEFREE |
In this study we examined the potential of three intrinsically fluorescent benzo[α]phenoxazines or BPZs (R=Cl, CH3, H) to induce cytotoxic autophagy in chemo and apoptosis-resistant, KRAS and p53 mutated pancreatic cancer model cell line, MIAPaCa-2.
|
27349450 |
2017 |
Pancreatic carcinoma
|
0.700 |
GeneticVariation
|
disease |
BEFREE |
We further show that class I HDACi induce senescence in pancreatic cancer cells with mutant p53.
|
27838375 |
2017 |
Pancreatic carcinoma
|
0.700 |
Biomarker
|
disease |
BEFREE |
Reprogramming pancreatic stellate cells via p53 activation: A putative target for pancreatic cancer therapy.
|
29211796 |
2017 |
Pancreatic carcinoma
|
0.700 |
GeneticVariation
|
disease |
BEFREE |
A combined approach targeting HDAC1/HDAC2 and MYC may present a novel and molecularly defined strategy to target mutant p53 in pancreatic cancer.
|
27721407 |
2017 |
Pancreatic carcinoma
|
0.700 |
Biomarker
|
disease |
BEFREE |
The expression of alpha-enolase, Ki67 and p53 in pancreatic cancer and adjacent normal tissues were evaluated by IHC using the corresponding primary antibodies on the commercial tissue arrays.
|
28824297 |
2017 |
Pancreatic carcinoma
|
0.700 |
Biomarker
|
disease |
BEFREE |
In contrast, all animals with CI-lacking TP53 developed various subtypes of PC, including acinar cell carcinoma, ductal adenocarcinoma, sarcomatoid carcinoma and neuroendocrine tumors, and all died within 65 weeks.
|
27991926 |
2017 |