نتایج جستجو برای: parp inhibitors

تعداد نتایج: 192891  

2013
Raquel E. Reinbolt John L. Hays

Gynecologic malignancies annually account for over 91,000 new cancer cases and approximately 28,000 deaths in the United States. Although there have been advancements in cytotoxic chemotherapies, there has not been significant improvement in overall survival in these patients. While targeted therapies have shown some benefit in many solid tumors, further development of these agents is needed fo...

2013
Maria Saveria Gilardini Montani Andrea Prodosmo Venturina Stagni Dania Merli Laura Monteonofrio Veronica Gatti Maria Pia Gentileschi Daniela Barilà Silvia Soddu

BACKGROUND Mutations in the DNA damage response (DDR) factors, breast cancer 1 (BRCA1) and BRCA2, sensitize tumor cells to poly(ADP-ribose) polymerase (PARP) inhibitors. The ataxia telangiectasia mutated (ATM) kinase is a key DDR protein whose heterozygous germline mutation is a moderate-risk factor for developing breast cancer. In this study, we examined whether ATM inactivation in breast canc...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 1999
C M Whitacre E Zborowska J K Willson N A Berger

Cleavage of poly(ADP-ribose) polymerase (PARP) by caspases is a prominent characteristic of apoptosis or programmed cell death shown to be induced by topoisomerase (Topo) inhibitors. Because Topo I inhibitors have been shown to be effective in the treatment of some patients with colon cancer, we considered the possibility of using PARP cleavage as an early predictor of responsiveness to this cl...

2012
Salomé C. Vilchez Larrea Teemu Haikarainen Mohit Narwal Mariana Schlesinger Harikanth Venkannagari Mirtha M. Flawiá Silvia H. Fernández Villamil Lari Lehtiö

Poly(ADP-ribosylation) is a post-translational covalent modification of proteins catalyzed by a family of enzymes termed poly(ADP-ribose) polymerases (PARPs). In the human genome, 17 different genes have been identified that encode members of the PARP superfamily. Poly (ADP-ribose) metabolism plays a role in a wide range of biological processes. In Trypanosoma cruzi, PARP enzyme appears to play...

Journal: :American journal of physiology. Renal physiology 2004
Martin J Mangino Mary Ametani Csaba Szabó James H Southard

The nuclear enzyme poly(ADP-ribose) polymerase (PARP) has been implicated in ischemia-reperfusion injury in many tissues under normothermic conditions. The purpose of this study was to determine whether PARP contributes to mechanisms of the hypothermic ischemia-reperfusion injury that occurs when kidneys are cold stored for transplantation. Cortical tissue slice PARP enzyme activity rose signif...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2007
Kapila Ratnam Jennifer A Low

Poly(ADP-ribose) polymerase (PARP) is a nuclear enzyme that signals the presence of DNA damage by catalyzing the addition of ADP-ribose units to DNA, histones, and various DNA repair enzymes and by facilitating DNA repair. PARP has been gaining increasing interest as a therapeutic target for many diseases and especially for cancer. Inhibition of PARP potentiates the activity of DNA-damaging age...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2000
A A Pieper S Blackshaw E E Clements D J Brat D K Krug A J White P Pinto-Garcia A Favit J R Conover S H Snyder A Verma

Poly(ADP-ribose) polymerase (PARP) transfers ADP ribose groups from NAD(+) to nuclear proteins after activation by DNA strand breaks. PARP overactivation by massive DNA damage causes cell death via NAD(+) and ATP depletion. Heretofore, PARP has been thought to be inactive under basal physiologic conditions. We now report high basal levels of PARP activity and DNA strand breaks in discrete neuro...

Journal: :Nucleic Acids Research 2006
Helen E. Bryant Thomas Helleday

Poly (ADP-ribose) polymerase (PARP-1), ATM and DNA-dependent protein kinase (DNA-PK) are all involved in responding to DNA damage to activate pathways responsible for cellular survival. Here, we demonstrate that PARP-1-/- cells are sensitive to the ATM inhibitor KU55933 and conversely that AT cells are sensitive to the PARP inhibitor 4-amino-1,8-napthalamide. In addition, PARP-1-/- cells are sh...

Journal: :Journal of Pharmaceutical Sciences 2014

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