Early effects of PP60v-src kinase activation on caveolae

Author(s):  
Young-Gyu Ko ◽  
Pingsheng Liu ◽  
Ravindra K. Pathak ◽  
Leonard C. Craig ◽  
Richard G. W. Anderson
2005 ◽  
Vol 65 (15) ◽  
pp. 6493-6497 ◽  
Author(s):  
Neslihan Cabioglu ◽  
Justin Summy ◽  
Claudia Miller ◽  
Nila U. Parikh ◽  
Aysegul A. Sahin ◽  
...  

2007 ◽  
Vol 67 (6) ◽  
pp. 2480-2489 ◽  
Author(s):  
Bostjan Humar ◽  
Ryuji Fukuzawa ◽  
Vanessa Blair ◽  
Anita Dunbier ◽  
Helen More ◽  
...  

Blood ◽  
2006 ◽  
Vol 109 (2) ◽  
pp. 497-499 ◽  
Author(s):  
Alfonso Quintas-Cardama ◽  
Hagop Kantarjian ◽  
Dan Jones ◽  
Claude Nicaise ◽  
Susan O'Brien ◽  
...  

Abstract Developing strategies to counteract imatinib resistance constitutes a challenge in chronic myelogenous leukemia (CML). Therapy with the tyrosine kinase inhibitors nilotinib (AMN107) and dasatinib (BMS-354825) has produced high rates of hematologic and cytogenetic response. Src kinase activation has been linked to Bcr-Abl–mediated leukemogenesis and CML progression. In addition to binding Abl kinase with less stringent conformational requirements than imatinib, dasatinib is a potent Src kinase inhibitor. In the current study, we report on 23 patients with CML (19 of them in accelerated or blastic phases) treated with dasatinib after treatment failure with both imatinib and nilotinib. More than half (13; 57%) of 23 patients responded to dasatinib: 10 (43%) had a complete hematologic response (CHR), including 7 (30%) who had a cytogenetic response (2 complete, 4 partial, and 1 minor). These results suggest that dasatinib may be active in some patients after failure with both imatinib and nilotinib.


2019 ◽  
Vol 26 (8) ◽  
pp. 1081-1094.e6 ◽  
Author(s):  
Jennifer E. Klomp ◽  
Mark Shaaya ◽  
Jacob Matsche ◽  
Rima Rebiai ◽  
Jesse S. Aaron ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document