Results 121 to 130 of about 7,834 (208)

885 Characterization of the tumor microenvironment in advanced breast cancer patients treated with talazoparib followed by combination of talazoparib and avelumab

open access: yesRegular and Young Investigator Award Abstracts, 2023
Edward T Richardson   +18 more
openaire   +2 more sources

Integrating PARP Inhibitors in mCRPC Therapy: Current Strategies and Emerging Trends

open access: yesCancer Management and Research
Bicky Thapa,1,* Navonil De Sarkar,2– 4,* Subhajit Giri,2,3 Komal Sharma,2– 4 Mingee Kim,5 Deepak Kilari1 1Division of Hematology and Oncology, Medical College of Wisconsin, Milwaukee, WI, USA; 2Medical College of Wisconsin Cancer Center ...
Thapa B   +5 more
doaj  

Exploring the role of PARP1 inhibition in enhancing antibody–drug conjugate therapy for acute leukemias: insights from DNA damage response pathway interactions

open access: yesJournal of Translational Medicine
Background The introduction of antibody–drug conjugates represents a significant advancement in targeted therapy of acute myeloid leukemia (AML) and acute lymphoblastic leukemia (ALL).
Andrea Ghelli Luserna di Rorà   +22 more
doaj   +1 more source

A REVIEW ARTICLE ON TALAZOPARIB – ANTI CANCER DRUG

open access: yes
Talazoparib tosylate (BMN-673, Talzenna; Pfizer) is an oral poly [ADP-ribose] polymerase (PARP) inhibitor (PARPi) that has been approved by the U.S. Food and Drug Administration (FDA) and the European Medicines Agency (EMA) for the treatment of germline BRCA-mutated locally advanced or metastatic breast cancer (BC). In preclinical and clinical studies,
openaire   +1 more source

Resistance to neoadjuvant talazoparib in triple-negative breast cancer by BRN2-induced ATR/STAT3 pathways or SHLD2 subclone expansion. [PDF]

open access: yesProc Natl Acad Sci U S A
Abdulkareem NM   +14 more
europepmc   +1 more source

PARP1 trapping activates cGAS-STING pathway to induce immunogenic cell death in multiple myeloma. [PDF]

open access: yesCancer Cell Int
Juli G   +11 more
europepmc   +1 more source

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