John Jeffrey Talley
Ironwood Pharmaceuticals
Network
Latest external collaboration on country level. Dive into details by clicking on the dots.
Publication
Featured researches published by John Jeffrey Talley.
Cancer Research | 2017
Bobby W. Sandage; John Jeffrey Talley; Eduardo J. Martinez; Maryland Franklin; Mary Anne Meade; Dan Saims; Matt Thayer; Scott C. Wise; David Draper; Wilber Leopold
Objective: The objective of this study was to evaluate the effect of ECP1014, a new selective COX2 inhibitor, in combination with a PDL1 inhibitor on tumor growth in a CT26 murine colon carcinoma model. Colon cancer has been described as a “cold tumor” and antiPDL1monotherapy has shown limited or no benefit. In addition, many colon cancer cell lines produce high levels of PGE2, which may in turn dampen the immune system. The hypothesis was that combining ECP1014, which we have shown potently decreases PGE2 in CT26, with a checkpoint inhibitor would increase immune response to the tumor, turning it “hot” and producing superior tumor control versus either agent alone. Methods: Balb/C mice were implanted with CT26 cells and randomly assigned to 7 treatment groups; vehicle (G1), 10mg/kg rat IgG2b control (G2), 10mg/kg antiPDL1 (G3), 10mg/kg ECP1014 (G4), 10mg/kg ECP1014+10mg/kg rat IgG2b (G5), 10mg/kg ECP1014+10mg/kg antiPDL1 (G6), 1mg/kg ECP1014+10mg/kg antiPDL1(G7). ECP1014 was given daily by oral gavage; rat IgG2b and antiPDL1 (clone 10F.9G2) were administered IP. Treatment was started on day 3 post implant and mice were followed for 16 days. Tumor measurements were taken every 2 to 3 days, and a nonparametric approach was taken to assess the pairwise differences among groups using day 16 tumor volumes. In addition, a responder analysis was used. Tumor infiltrating lymphocytes (TIL) were also assessed by flow cytometry on day 16. Results: All animals developed tumors. G4 to 7 demonstrated statistically significantly (p Summary: ECP1014 alone was superior to antiPDL1 in slowing tumor growth. However, the combination of ECP1014+antiPDL1showed the greatest tumor response and growth suppression and markedly increased CD8+ Tcells infiltrating into the tumor vs. single agent anti-PDL1 treatment. Citation Format: Bobby W. Sandage, John J. Talley, Eduardo J. Martinez, Maryland R. Franklin, Mary Anne Meade, Dan Saims, Matt Thayer, Scott Wise, David Draper, Wilber Leopold. Combination of ECP1014 and anti-PD-L1 reduces tumor growth in the CT26 murine colon carcinoma model of a cold tumor [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2017; 2017 Apr 1-5; Washington, DC. Philadelphia (PA): AACR; Cancer Res 2017;77(13 Suppl):Abstract nr 2619. doi:10.1158/1538-7445.AM2017-2619
Archive | 2006
Wilmin Bartolini; Brian Cali; Barbara Chen; Yueh-Tyng Chien; Mark G. Currie; G. Milne; James Philip Pearson; John Jeffrey Talley; Jing Yang; Craig Zimmerman; Alex Monreal
American Journal of Nursing | 2004
Brian M. Cali; Yueh-Tyng Chien; Mark G. Currie; John Jeffrey Talley; Craig Zimmerman
Archive | 2004
Eduardo J. Martinez; John Jeffrey Talley; Stephen Antonelli; Timothy C. Barden; Regina Lundrigan-Soucy; Wayne C. Schairer; Jing-Jing Yang; Daniel P. Zimmer; Brian M. Cali; Mark G. Currie; Peter S. Yorgey
Archive | 2006
Eduardo J. Martinez; John Jeffrey Talley; Regina Lundrigan
Archive | 2004
John Jeffrey Talley; Angelika Fretzen; Craig Zimmerman; Timothy C. Barden; Jing Jing Yang; Eduardo J. Martinez; Robert W. Busby; Etchell A. Cordero; Fariba Houman Cipriano; Christine M. Pierce; Eric Summers
Archive | 2006
John Jeffrey Talley; Eduardo J. Martinez; Daniel P. Zimmer; Regina Lundrigan-Soucy
Archive | 2006
Stephen Antonelli; Regina Lundrigan; Eduardo J. Martinez; Wayne C. Schairer; John Jeffrey Talley; Timothy C. Barden; Jing-Jing Yang; Daniel P. Zimmer
Archive | 2004
Eduardo J. Martinez; John Jeffrey Talley
Archive | 2006
Eduardo J. Martinez; John Jeffrey Talley; Daniel P. Zimmer