Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Katherine Paweletz"'
Publikováno v:
Journal of Clinical Oncology. 38:155-155
155 Background: AMG 160 is an HLE BiTE immune therapy that binds prostate-specific membrane antigen (PSMA) on tumor cells and CD3 on T cells, leading to T cell activation, cytokine production, and tumor cell lysis. A phase 1 study of AMG 160 in patie
Autor:
Ian McCaffery, Susan Swift, Stephen Kaufman, C. Glenn Begley, Leigh Busse, Liqin Liu, Steven G. Elliott, Angus M. Sinclair, Angela Coxon, Katherine Paweletz
Publikováno v:
Blood. 115:4264-4272
Erythropoiesis stimulating agents (ESAs) have been reported to activate erythropoietin receptors (EpoR) on cell types, including endothelial, neuronal, renal tubule, and cardiac cells. ESAs have also been reported to promote angiogenesis. However, th
Publikováno v:
Journal for Immunotherapy of Cancer
Meeting abstracts Cytotoxic CD8+ T lymphocytes (CTL) mediate target cell killing of tumor cells. New technological advances in multi-parameter flow cytometry have enabled the detection and enumeration of antigen-specific CD8+ T cells (MHC-class I dex
Autor:
Robert D. Loberg, Katherine Paweletz, Abraham Anderson, Gregory Friberg, Florian D. Vogl, Erick Gamelin, Gloria Juan
Publikováno v:
Cancer Research. 76:439-439
Purpose: Aurora kinases are associated with acquired resistance to therapy in human cancers. We hypothesized that AURKA amplification is a late event in ovarian cancer (OC) progression and that frequency of amplification might be underestimated if as
Autor:
Minghan Wang, John M. Rossi, Maurice Emery, Edgar Bautista, Oranee Daniels, Riccardo Perfetti, Katherine Paweletz, Anna Akrami, Marc R. Gastonguay, Megan A. Gibbs, John P. Gibbs, Ian McCaffery, Brian H. Smith
Publikováno v:
Journal of clinical pharmacology. 51(6)
Inhibition of 11β-HSD1 is hypothesized to improve measures of insulin sensitivity and hepatic glucose output in patients with type II diabetes. AMG 221 is a potent, small molecule inhibitor of 11β-HSD1. The objective of this analysis is to describe
Autor:
Katherine Paweletz, Leigh Busse, C. Glenn Begley, Ian McCaffery, V. Dan Fitzpatrick, Scott D. Patterson, Steve Elliott, John M. Rossi
Publikováno v:
PLoS ONE, Vol 10, Iss 3, p e0122149 (2015)
PLoS ONE
PLoS ONE
Several clinical trials in oncology have reported increased mortality or disease progression associated with erythropoiesis-stimulating agents. One hypothesis proposes that erythropoiesis-stimulating agents directly stimulate tumor proliferation and/
Autor:
John Rossi, Robert D. Loberg, Michael B. Bass, Chetan Deshpande, Dan Baker, Maha Rizk, Katherine Paweletz, Michael A. Damore, Scott D. Patterson, Ian McCaffery
Publikováno v:
Cancer Research. 73:1105-1105
Redundancy in growth factor (GF) pathway utilization in human tumors has been hypothesized to be a primary resistance mechanism to targeted therapeutics. Little evidence has been reported in primary tumors to demonstrate functional differences betwee
Autor:
Raffi Manoukian, Katherine Paweletz, Shen-Wu Wang, John M. Rossi, Robert D. Loberg, Beate Sable, Yanyan Tudor, Ian McCaffery, Scott D. Patterson
Publikováno v:
Blood. 118:4783-4783
Abstract 4783 Recently, clinical studies were conducted in chronic kidney disease of type 2 diabetes patients that suggested an increased risk of stroke in patients receiving Erythropoiesis Stimulating Agents (ESAs) compared to placebo. One proposed
Autor:
Ian McCaffery, Scott D. Patterson, V. Dan Fitzpatrick, Katherine Paweletz, Steve Elliott, Yanyan Tudor, C. Glenn Begley, John M. Rossi
Publikováno v:
Blood. 118:4781-4781
Abstract 4781 Several clinical trials have reported increased mortality or disease progression associated with erythropoiesis-stimulating agents (ESA) in patients with cancer. One hypothesis proposes that ESAs stimulate tumor proliferation and or sur
Autor:
Ian McCaffery, Scott D. Patterson, Steven G. Elliott, Yanyan Tudor, Katherine Paweletz, John M. Rossi, V. D. Fitzpatrick
Publikováno v:
Journal of Clinical Oncology. 27:11104-11104
11104 Background: EpoR mRNA and protein expression have been reported at low levels in human tumors implying EpoR may be functional in tumor cells with inferred implications for the use of erythropoiesis stimulating agents in the Oncology setting. Ho