Cross-platform pathway-based analysis identifies markers of response to the PARP inhibitor olaparib.
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In vitro human cell line models to predict clinical response to anticancer drugsEffect of MRE11 loss on PARP-inhibitor sensitivity in endometrial cancer in vitroVeliparib Alone or in Combination with Mitomycin C in Patients with Solid Tumors With Functional Deficiency in Homologous Recombination Repair.ATM-depletion in breast cancer cells confers sensitivity to PARP inhibition.XI-006 induces potent p53-independent apoptosis in Ewing sarcoma.Lack of MRE11-RAD50-NBS1 (MRN) complex detection occurs frequently in low-grade epithelial ovarian cancer.Comparative antiproliferative effects of iniparib and olaparib on a panel of triple-negative and non-triple-negative breast cancer cell linesDoubling down on the PI3K-AKT-mTOR pathway enhances the antitumor efficacy of PARP inhibitor in triple negative breast cancer model beyond BRCA-nessRAD51 inhibition in triple negative breast cancer cells is challenged by compensatory survival signaling and requires rational combination therapy.Triple-negative breast cancer: bridging the gap from cancer genomics to predictive biomarkers.Olaparib: first global approval.Replication-induced DNA damage after PARP inhibition causes G2 delay, and cell line-dependent apoptosis, necrosis and multinucleation.Opportunities for the repurposing of PARP inhibitors for the therapy of non-oncological diseases.Quantitative measurement of alterations in DNA damage repair (DDR) pathways using single cell network profiling (SCNP)Neoadjuvant Therapy for Breast Cancer: Established Concepts and Emerging Strategies.Cumulative defects in DNA repair pathways drive the PARP inhibitor response in high-grade serous epithelial ovarian cancer cell lines.Heterogeneous drug penetrance of veliparib and carboplatin measured in triple negative breast tumors.DNA repair deficiency biomarkers and the 70-gene ultra-high risk signature as predictors of veliparib/carboplatin response in the I-SPY 2 breast cancer trial.Cytokeratin 5/6, c-Met expressions, and PTEN loss prognostic indicators in triple-negative breast cancer.RBR-type E3 ubiquitin ligase RNF144A targets PARP1 for ubiquitin-dependent degradation and regulates PARP inhibitor sensitivity in breast cancer cells.Pathway-Enriched Gene Signature Associated with 53BP1 Response to PARP Inhibition in Triple-Negative Breast Cancer.PARP inhibitors: the journey from research hypothesis to clinical approval.CRISPR screens identify genomic ribonucleotides as a source of PARP-trapping lesions
P2860
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P2860
Cross-platform pathway-based analysis identifies markers of response to the PARP inhibitor olaparib.
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
@zh
2012年论文
@zh-cn
name
Cross-platform pathway-based a ...... o the PARP inhibitor olaparib.
@ast
Cross-platform pathway-based a ...... o the PARP inhibitor olaparib.
@en
type
label
Cross-platform pathway-based a ...... o the PARP inhibitor olaparib.
@ast
Cross-platform pathway-based a ...... o the PARP inhibitor olaparib.
@en
prefLabel
Cross-platform pathway-based a ...... o the PARP inhibitor olaparib.
@ast
Cross-platform pathway-based a ...... o the PARP inhibitor olaparib.
@en
P2093
P2860
P50
P1476
Cross-platform pathway-based a ...... o the PARP inhibitor olaparib.
@en
P2093
Anneleen Daemen
Denise M Wolf
James E Korkola
Jessica R Frankum
Joe W Gray
Lakshmi R Jakkula
Laura J van't Veer
Nicholas J Wang
Paul T Spellman
Rachel Brough
P2860
P2888
P304
P356
10.1007/S10549-012-2188-0
P407
P577
2012-08-09T00:00:00Z