| Literature DB >> 21930909 |
Romel Somwar1, Hediye Erdjument-Bromage, Erik Larsson, David Shum, William W Lockwood, Guangli Yang, Chris Sander, Ouathek Ouerfelli, Paul J Tempst, Hakim Djaballah, Harold E Varmus.
Abstract
We previously described four small molecules that reduced the growth of lung adenocarcinoma cell lines with either epidermal growth factor receptor (EGFR) or KRAS mutations in a high-throughout chemical screen. By combining affinity proteomics and gene expression analysis, we now propose superoxide dismutase 1 (SOD1) as the most likely target of one of these small molecules, referred to as lung cancer screen 1 (LCS-1). siRNAs against SOD1 slowed the growth of LCS-1 sensitive cell lines; conversely, expression of a SOD1 cDNA increased proliferation of H358 cells and reduced sensitivity of these cells to LCS-1. In addition, SOD1 enzymatic activity was inhibited in vitro by LCS-1 and two closely related analogs. These results suggest that SOD1 is an LCS-1-binding protein that may act in concert with mutant proteins, such as EGFR and KRAS, to promote cell growth, providing a therapeutic target for compounds like LCS-1.Entities:
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Year: 2011 PMID: 21930909 PMCID: PMC3182729 DOI: 10.1073/pnas.1113554108
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205