Serveur d'exploration sur Pittsburgh

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Linifanib (ABT-869), enhances cytotoxicity with poly (ADP-ribose) polymerase inhibitor, veliparib (ABT-888), in head and neck carcinoma cells.

Identifieur interne : 002433 ( Main/Exploration ); précédent : 002432; suivant : 002434

Linifanib (ABT-869), enhances cytotoxicity with poly (ADP-ribose) polymerase inhibitor, veliparib (ABT-888), in head and neck carcinoma cells.

Auteurs : Heng-Wei Hsu [États-Unis] ; Rosalia De Necochea-Campion [États-Unis] ; Vonetta Williams [États-Unis] ; Penelope J. Duerksen-Hughes [États-Unis] ; Alfred A. Simental [États-Unis] ; Robert L. Ferris [États-Unis] ; Chien-Shing Chen [États-Unis] ; Saied Mirshahidi [États-Unis]

Source :

RBID : pubmed:24735547

Descripteurs français

English descriptors

Abstract

PARP inhibitors (PARPi) may provide an opportunity to gain selective killing of tumor cells which have deficiencies in cellular DNA repair systems. We previously demonstrated linifanib (ABT-869), a multi-receptor tyrosine kinase inhibitor of VEGF and PDGF receptor families, radiosensitized Head and Neck Squamous Cell Carcinoma cells (HNSCC) via inhibiting STAT3 activation. Given that STAT3 can modulate DNA damage response (DDR) pathway, in this study, we evaluate the effects of linifanib to enhance cytotoxicity with the PARPi, veliparib (ABT-888), in HNSCC.

DOI: 10.1016/j.oraloncology.2014.03.006
PubMed: 24735547


Affiliations:


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Le document en format XML

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<term>Carcinoma, Squamous Cell (drug therapy)</term>
<term>Cell Line, Tumor</term>
<term>Cell Survival (drug effects)</term>
<term>DNA Breaks (drug effects)</term>
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<term>Cassures de l'ADN ()</term>
<term>Histone (métabolisme)</term>
<term>Humains</term>
<term>Indazoles (pharmacologie)</term>
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<div type="abstract" xml:lang="en">PARP inhibitors (PARPi) may provide an opportunity to gain selective killing of tumor cells which have deficiencies in cellular DNA repair systems. We previously demonstrated linifanib (ABT-869), a multi-receptor tyrosine kinase inhibitor of VEGF and PDGF receptor families, radiosensitized Head and Neck Squamous Cell Carcinoma cells (HNSCC) via inhibiting STAT3 activation. Given that STAT3 can modulate DNA damage response (DDR) pathway, in this study, we evaluate the effects of linifanib to enhance cytotoxicity with the PARPi, veliparib (ABT-888), in HNSCC.</div>
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