6SCM

SOS1 in Complex with Inhibitor BI-3406

6SCM の概要

• エントリーDOI: 10.2210/pdb6scm/pdb
• 分子名称: Son of sevenless homolog 1, IMIDAZOLE, 1,2-ETHANEDIOL, ... (5 entities in total)
• 機能のキーワード: oncology, exchange factor, protein-ligand complex, oncoprotein
• 由来する生物種: Homo sapiens (Human)
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 58014.26

構造登録者

Kessler, D.,Fischer, G.,Ramharter, J. (登録日: 2019-07-24, 公開日: 2020-08-26, 最終更新日: 2024-05-15)

主引用文献

Hofmann, M.H.,Gmachl, M.,Ramharter, J.,Savarese, F.,Gerlach, D.,Marszalek, J.R.,Sanderson, M.P.,Kessler, D.,Trapani, F.,Arnhof, H.,Rumpel, K.,Botesteanu, D.A.,Ettmayer, P.,Gerstberger, T.,Kofink, C.,Wunberg, T.,Zoephel, A.,Fu, S.C.,Teh, J.L.,Bottcher, J.,Pototschnig, N.,Schachinger, F.,Schipany, K.,Lieb, S.,Vellano, C.P.,O'Connell, J.C.,Mendes, R.L.,Moll, J.,Petronczki, M.,Heffernan, T.P.,Pearson, M.,McConnell, D.B.,Kraut, N.
BI-3406, a Potent and Selective SOS1-KRAS Interaction Inhibitor, Is Effective in KRAS-Driven Cancers through Combined MEK Inhibition.
Cancer Discov, 11:142-157, 2021

PubMed Abstract: is the most frequently mutated driver of pancreatic, colorectal, and non-small cell lung cancers. Direct KRAS blockade has proved challenging, and inhibition of a key downstream effector pathway, the RAF-MEK-ERK cascade, has shown limited success because of activation of feedback networks that keep the pathway in check. We hypothesized that inhibiting SOS1, a KRAS activator and important feedback node, represents an effective approach to treat KRAS-driven cancers. We report the discovery of a highly potent, selective, and orally bioavailable small-molecule SOS1 inhibitor, BI-3406, that binds to the catalytic domain of SOS1, thereby preventing the interaction with KRAS. BI-3406 reduces formation of GTP-loaded RAS and limits cellular proliferation of a broad range of KRAS-driven cancers. Importantly, BI-3406 attenuates feedback reactivation induced by MEK inhibitors and thereby enhances sensitivity of KRAS-dependent cancers to MEK inhibition. Combined SOS1 and MEK inhibition represents a novel and effective therapeutic concept to address KRAS-driven tumors. SIGNIFICANCE: To date, there are no effective targeted pan-KRAS therapies. In-depth characterization of BI-3406 activity and identification of MEK inhibitors as effective combination partners provide an attractive therapeutic concept for the majority of KRAS-mutant cancers, including those fueled by the most prevalent mutant KRAS oncoproteins, G12D, G12V, G12C, and G13D...

PubMed: 32816843
DOI: 10.1158/2159-8290.CD-20-0142

実験手法

X-RAY DIFFRACTION (1.866 Å)