摘要: Gene transcription mechanisms are critical control points for cell function and differentiation as well as disease pathology. It has remained difficult to target gene transcription mechanisms with small molecule drugs due in part to the role of protein-protein interactions in transcription complexes. RhoA/C- GTPase regulation of the serum responsive transcription factor complex involving serum response factor (SRF) and myocardin-related transcription factor (MRTF) plays a key role in cancer and fibrotic mechanisms. In an attempt to disrupt this critical gene transcription mechanism, we undertook a high-throughput ″pathway screen″ using an SRE-Luciferase reporter which was activated by transient transfection of HEK293 cells with Ga13, an up- stream activator of RhoA and RhoC. The Rho/MRTF inhibitor tool compound CCG-1423 was identified in this screen. It and analogs such as CCG-203971 have been used extensively to disrupt myofibroblast activation and tissue fibrosis as well as melanoma cell migration and metastasis. In the present study, we have used immobilized compounds and mass spectroscopy to identify the molecular target of the CCG-203971 series of anti-fibrotic and anti-meta?static agents. It is a poorly studied intranuclear protein that participates in gene transcription regulation by NF-κB and MRTF/SRF mechanisms. This dual mechanism rationalizes the strong efficacy of CCG-203971 and related compounds as anti-fibrotic and anti-metastatic agents. The identification of a molecular target also greatly facilitates future compound development through structure- based drug discovery and target biology evaluation.