Results 31 to 40 of about 34,135 (204)

GBM radiosensitizers: dead in the water…or just the beginning? [PDF]

open access: yes, 2017
The finding that most GBMs recur either near or within the primary site after radiotherapy has fueled great interest in the development of radiosensitizers to enhance local control.
Bindra, Ranjit S.   +3 more
core   +1 more source

A Quaternary Solid Dispersion System for Improving the Solubility of Olaparib

open access: yesSolids
To improve the low solubility of poorly water soluble olaparib, in the following study, we prepared olaparib-loaded quaternary solid dispersions with hypromellose, Tween 20 or Labrasol, and colloidal silica.
Tae-Han Yun   +4 more
doaj   +1 more source

MiR-509-3 augments the synthetic lethality of PARPi by regulating HR repair in PDX model of HGSOC

open access: yesJournal of Hematology & Oncology, 2020
Background PARP inhibitors have been the most promising target drugs with widely proven benefits among ovarian cancer patients. Although platinum-response, HR-related genes, or HRD genomic scar detection are acceptably used in assessment of Olaparib ...
Chenggong Sun   +10 more
doaj   +1 more source

Correlation between molar activity, injection mass and uptake of the PARP targeting radiotracer [18F]olaparib in mouse models of glioma

open access: yesEJNMMI Research, 2022
Purpose Radiopharmaceuticals targeting poly(ADP-ribose) polymerase (PARP) have emerged as promising agents for cancer diagnosis and therapy. PARP enzymes are expressed in both cancerous and normal tissue.
Chung Ying Chan   +13 more
doaj   +1 more source

Oligo-Fucoidan supplementation enhances the effect of Olaparib on preventing metastasis and recurrence of triple-negative breast cancer in mice

open access: yesJournal of Biomedical Science, 2022
Background Seaweed polysaccharides have been recommended as anticancer supplements and for boosting human health; however, their benefits in the treatment of triple-negative breast cancers (TNBCs) and improving immune surveillance remain unclear ...
Li-Mei Chen   +7 more
doaj   +1 more source

Long-term responders on olaparib maintenance in high-grade serous ovarian cancer: Clinical and molecular characterization [PDF]

open access: yes, 2017
Purpose: Maintenance therapy with olaparib has improved progression-free survival in women with high-grade serous ovarian cancer (HGSOC), particularly those harboring BRCA1/2 mutations.
Barrett, J. Carl   +22 more
core   +2 more sources

Antitumor activity and safety of the PARP inhibitor rucaparib in patients with high grade ovarian carcinoma and a germline or somatic BRCA1 or BRCA2 mutation: integrated analysis of data from Study 10 and ARIEL2 [PDF]

open access: yes, 2017
Objective: An integrated analysis was undertaken to characterize the antitumor activity and safety profile of the oral poly(ADP-ribose) polymerase inhibitor rucaparib in patients with relapsed high-grade ovarian carcinoma (HGOC). Methods: Eligible
Bell-McGuinn, Katherine   +24 more
core   +1 more source

Evolutionary dynamics of cancer multidrug resistance in response to olaparib and photodynamic therapy

open access: yesTranslational Oncology, 2021
P-glycoprotein (P-gp) is an adenosine triphosphate (ATP)-dependent drug efflux protein commonly associated with multidrug resistance in cancer chemotherapy.
Yan Baglo   +6 more
doaj   +1 more source

Evaluation of the radiosensitizing potency of chemotherapeutic agents in prostate cancer cells [PDF]

open access: yes, 2016
PURPOSE: Despite recent advances in the treatment of metastatic prostate cancer, survival rates are low and treatment options are limited to chemotherapy and hormonal therapy.
Mairs, Robert J., Rae, Colin
core   +2 more sources

IGFBP3 promotes resistance to Olaparib via modulating EGFR signaling in advanced prostate cancer

open access: yesiScience
Summary: Olaparib is a pioneering PARP inhibitor (PARPi) approved for treating castration-resistant prostate cancer (CRPC) tumors harboring DNA repair defects, but clinical resistance has been documented.
Amy R. Leslie   +10 more
doaj   +1 more source

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