Combined Tyrosine and Serine/Threonine Kinase Inhibition by Sorafenib Prevents Progression of Experimental Pulmonary Hypertension and Myocardial Remodeling
Author(s) -
Martina I. Klein,
Ralph T. Schermuly,
Peter Ellinghaus,
Hendrik Milting,
Bernd Riedl,
Sevdaliikolova,
Soni Savai Pullamsetti,
Norbert Weißmann,
Eva Dony,
Rajkumar Savai,
Hossein A. Ghofrani,
Friedrich Grimminger,
Andreas Büsch,
Stefan Schäfer
Publication year - 2008
Publication title -
circulation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.795
H-Index - 607
eISSN - 1524-4539
pISSN - 0009-7322
DOI - 10.1161/circulationaha.108.779751
Subject(s) - sorafenib , medicine , pulmonary hypertension , imatinib , tyrosine kinase , tyrosine kinase inhibitor , kinase , pharmacology , cardiology , endocrinology , receptor , chemistry , biochemistry , cancer , myeloid leukemia , hepatocellular carcinoma
Inhibition of tyrosine kinases, including platelet-derived growth factor receptor, can reduce pulmonary arterial pressure in experimental and clinical pulmonary hypertension. We hypothesized that inhibition of the serine/threonine kinases Raf-1 (also termed c-Raf) and b-Raf in addition to inhibition of tyrosine kinases effectively controls pulmonary vascular and right heart remodeling in pulmonary hypertension.
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