TY - JOUR
T1 - A Small-Molecule Pan-Id Antagonist Inhibits Pathologic Ocular Neovascularization
AU - Wojnarowicz, Paulina M.
AU - Lima e Silva, Raquel
AU - Ohnaka, Masayuki
AU - Lee, Sang Bae
AU - Chin, Yvette
AU - Kulukian, Anita
AU - Chang, Sung Hee
AU - Desai, Bina
AU - Garcia Escolano, Marta
AU - Shah, Riddhi
AU - Garcia-Cao, Marta
AU - Xu, Sijia
AU - Kadam, Rashmi
AU - Goldgur, Yehuda
AU - Miller, Meredith A.
AU - Ouerfelli, Ouathek
AU - Yang, Guangli
AU - Arakawa, Tsutomu
AU - Albanese, Steven K.
AU - Garland, William A.
AU - Stoller, Glenn
AU - Chaudhary, Jaideep
AU - Norton, Larry
AU - Soni, Rajesh Kumar
AU - Philip, John
AU - Hendrickson, Ronald C.
AU - Iavarone, Antonio
AU - Dannenberg, Andrew J.
AU - Chodera, John D.
AU - Pavletich, Nikola
AU - Lasorella, Anna
AU - Campochiaro, Peter A.
AU - Benezra, Robert
N1 - Publisher Copyright:
© 2019 The Author(s)
PY - 2019/10/1
Y1 - 2019/10/1
N2 - Wojnarowicz et al., describe the identification, by an in silico screen, and characterization of a small molecule, AGX51, that targets Id proteins. AGX51 treatment of cells lead to Id protein degradation, cell cycle arrest, and reduced cell viability. AGX51 inhibited pathologic ocular neovascularization in mouse models, phenocopying genetic Id loss.
AB - Wojnarowicz et al., describe the identification, by an in silico screen, and characterization of a small molecule, AGX51, that targets Id proteins. AGX51 treatment of cells lead to Id protein degradation, cell cycle arrest, and reduced cell viability. AGX51 inhibited pathologic ocular neovascularization in mouse models, phenocopying genetic Id loss.
KW - Id proteins
KW - angiogenesis
KW - macular degeneration
KW - protein-protein interactions
KW - retinopathy of prematurity
UR - http://www.scopus.com/inward/record.url?scp=85072314164&partnerID=8YFLogxK
U2 - 10.1016/j.celrep.2019.08.073
DO - 10.1016/j.celrep.2019.08.073
M3 - Article
AN - SCOPUS:85072314164
SN - 2211-1247
VL - 29
SP - 62-75.e7
JO - Cell Reports
JF - Cell Reports
IS - 1
ER -