z-logo
open-access-imgOpen Access
Topical Antiangiogenic SRPK1 Inhibitors Reduce Choroidal Neovascularization in Rodent Models of Exudative AMD
Author(s) -
Melissa V. Gammons,
O. Fedorov,
David Ivison,
Chunyun Du,
Tamsyn Clark,
Claire Hopkins,
Masatoshi Hagiwara,
Andrew D. Dick,
Russell J. Cox,
Steven J. Harper,
Jules C. Hancox,
Stefan Knapp,
David O. Bates
Publication year - 2013
Publication title -
investigative ophthalmology and visual science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.935
H-Index - 218
eISSN - 1552-5783
pISSN - 0146-0404
DOI - 10.1167/iovs.13-12422
Subject(s) - choroidal neovascularization , in vivo , pharmacology , angiogenesis , alternative splicing , kinase , neovascularization , serine , chemistry , vascular endothelial growth factor , rna splicing , phosphorylation , gene isoform , cancer research , biology , retinal , biochemistry , vegf receptors , gene , genetics , rna
Exudative AMD (wet AMD) is treated by monthly injection into the eye of anti-VEGF proteins. VEGF is alternatively spliced to produce numerous isoforms that differ in angiogenic activity. Serine-rich protein kinase-1 (SRPK1) has been identified as a regulator of pro-angiogenic VEGF splicing by phosphorylating serine-rich splicing factor-1 (SRSF1), which binds to VEGF pre-mRNA. We tested the hypothesis that topical (eye drop) SRPK1-selective inhibitors could be generated that reduce pro-angiogenic isoforms, and prevent choroidal neovascularization in vivo.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom