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A time-resolved live cell imaging assay to identify small molecule inhibitors of FGF2 signaling.

FEBS letters (2019-05-29)
Mennatallah Ahmed, Cyril Legrand, Ana Yagüe Relimpio, Carlo A Beretta, Alina Muschko, Sabine Wegehingel, Hans-Michael Müller, Peter Sehr, David W Will, Joe D Lewis, Walter Nickel
ABSTRAKT

Fibroblast growth factor 2 (FGF2) is a cell survival factor with crucial functions in tumor-induced angiogenesis. Here, we describe a novel time-resolved FGF2 signaling assay based upon live cell imaging of neuroblastoma cells. To validate this system, we tested 8960 small molecules for inhibition of FGF2 signaling with kinetic resolution. Hit compounds were validated in dose-response experiments for FGF2 signaling, FGF receptor antagonism, downstream ERK phosphorylation and FGF2-dependent chemoresistance in a cellular leukemia model system. The new screening system for FGF2 signaling inhibitors has unique features, deselecting compounds with pleiotropic effects on cell proliferation and, along with the experimental pipeline reported, great potential for the discovery of new classes of FGF2 signaling inhibitors that block FGF2 dependent tumor cell survival.

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Sigma-Aldrich
RPMI-1640 Medium, With L-glutamine and sodium bicarbonate, liquid, sterile-filtered, suitable for cell culture
Sigma-Aldrich
Anti-Fibroblast Growth Factor-Basic antibody, Mouse monoclonal, clone FB-8, purified from hybridoma cell culture