Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Because many variants cannot be detected in DNA from blood, testing tumor DNA as the first step can double the identification rate of patients who stand to benefit most from PARP inhibitors.
|
31076742 |
2020 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
PARG regulates the proliferation and differentiation of DCs and T cells via PARP/NF‑κB in tumour metastases of colon carcinoma.
|
30864743 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
We propose that combined blockade of ATR and PARP is an effective strategy for GBM, even for low-Myc GSCs that do not respond to PARPi alone, and potentially other PARPi-refractory tumors.
|
31266951 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
In conclusion, our data support DAXX as a modulator of DNA damage repair and suppressor of TNBC progression to sensitize tumors to the PARP inhibitor by repressing RAD51 functions.
|
31029033 |
2019 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Nevertheless, we observed a decrease in PCNA expression and a greater number of apoptotic index, higher expression of caspase 3, cleaved PARP and cleaved caspase 8 in tumors, confirming the activation of the extrinsic pathway of apoptosis by the combined treatment.
|
30738018 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Currently, inhibitors of immune tolerance and immune checkpoint inhibitors; PARP inhibitors; novel cytotoxic chemotherapies, such as trifluridine/tipiracil; and modifiers of the tumor microenvironment, such as pegylated hyaluronidase, are in clinical trials for the treatment of pancreatic cancer.
|
30681819 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Furthermore, while PARP inhibitors have demonstrated a clear role in treating tumors with underlying homologous recombination deficiencies, there is now biological and early clinical evidence to support their use in other molecular subsets of cancer, including tumors associated with high levels of replication stress such as small-cell lung cancer.
|
30760478 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Moreover, Inotodiol notably induced tumor cell apoptosis by Annexin-V-FITC apoptosis assay, which is associated with activation pro-apoptotic proteins of PARP, cleaved caspase-3 and Bax expression, inhibition anti-apoptotic protein Bcl-2 expression.
|
31128995 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
SIGNIFICANCE: This work demonstrates cross-talk between PARP inhibition and the tumor microenvironment related to STING/TBK1/IRF3 pathway activation in cancer cells that governs CD8<sup>+</sup> T-cell recruitment and antitumor efficacy.
|
31015319 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
These findings have clinical significance, as the expression levels of p12 could be a predictive biomarker of tumor response to PARP inhibitors.
|
30470508 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
The PAC010 model showed increased cell proliferation (Ki-67 staining) and markers indicating survival (increased p-AKT, p-ERK and p-NF-kB65 and suppression of cleaved PARP).
|
30899378 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
PARP inhibition enhances tumor cell-intrinsic immunity in ERCC1-deficient non-small cell lung cancer.
|
30589644 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Tumor BRCA Test for Patients with Epithelial Ovarian Cancer: The Role of Molecular Pathology in the Era of PARP Inhibitor Therapy.
|
31653094 |
2019 |
Neoplasms
|
0.100 |
GeneticVariation
|
group |
BEFREE |
Improved Therapeutic Window in <i>BRCA</i>-mutant Tumors with Antibody-linked Pyrrolobenzodiazepine Dimers with and without PARP Inhibition.
|
30352801 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
These findings suggest a new therapeutic strategy for ATM-mutant CRPC patients by targeting LDHA-mediated glycolysis metabolism, which might be effective for the PARP inhibitor resistant mCRPC tumors.
|
30400006 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Furthermore, the xenograft tumor model demonstrated significantly increases sensitivity towards PARP inhibition under NFBD1 deficiency.
|
30717758 |
2019 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Furthermore, EGCG suppressed tumor growth <i>in vivo</i> by downregulating the expression of miR-25 and proteins associated with apoptosis, which was further confirmed by a reduction of Ki-67 and increase of pro-apoptotic PARP expression as determined by immunohistochemistry staining.
|
31431131 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Moreover, established therapies such as DNA damaging treatments such as chemotherapy and PARP inhibitors further modify the tumor microenvironment.
|
31320901 |
2019 |
Neoplasms
|
0.100 |
GeneticVariation
|
group |
BEFREE |
<i>BRCA</i> Reversion Mutations in Circulating Tumor DNA Predict Primary and Acquired Resistance to the PARP Inhibitor Rucaparib in High-Grade Ovarian Carcinoma.
|
30425037 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Loss of ARID1A in Tumor Cells Renders Selective Vulnerability to Combined Ionizing Radiation and PARP Inhibitor Therapy.
|
31196855 |
2019 |
Neoplasms
|
0.100 |
GeneticVariation
|
group |
BEFREE |
We identified 8 patients and determined the impact of the specific DNA repair gene alterations on tumor response and time on treatment with PARP inhibition.
|
30099369 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Expert commentary: PARP inhibition could be a new therapeutic option for a number of tumors in the near future.
|
29260919 |
2018 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Furthermore, MENK could induce tumor cell apoptosis associated with the upregulation of Bax, a corresponding downregulation of BCL-2 and survivin, and activation of caspase-3 and PARP.
|
30425572 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
PARP inhibitors (PARPi) are potentially effective therapeutic agents capable of inducing synthetic lethality in tumors with deficiencies in homologous recombination (HR)-mediated DNA repair such as those carrying BRCA1 mutations.
|
29592899 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
The success of immune checkpoint inhibition in mismatch repair deficient tumors, PARP inhibitors for tumors with DNA repair defects, and targeting hyaluronan with PEGPH20 in patients with high expressing (hyaluronan-high) tumors are examples of promising biomarker-driven therapies.
|
30391013 |
2018 |