| Literature DB >> 20501857 |
Gerben Duns1, Eva van den Berg, Inge van Duivenbode, Jan Osinga, Harry Hollema, Robert M W Hofstra, Klaas Kok.
Abstract
Sporadic clear cell renal cell carcinoma (cRCC) is genetically characterized by the recurrent loss of the short arm of chromosome 3, with a hotspot for copy number loss in the 3p21 region. We applied a method called "gene identification by nonsense-mediated mRNA decay inhibition" to a panel of 10 cRCC cell lines with 3p21 copy number loss to identify biallelic inactivated genes located at 3p21. This revealed inactivation of the histone methyltransferase gene SETD2, located on 3p21.31, as a common event in cRCC cells. SETD2 is nonredundantly responsible for trimethylation of the histone mark H3K36. Consistent with this function, we observed loss or a decrease of H3K36me3 in 7 out of the 10 cRCC cell lines. Identification of missense mutations in 2 out of 10 primary cRCC tumor samples added support to the involvement of loss of SETD2 function in the development of cRCC tumors. Copyright 2010 AACR.Entities:
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Year: 2010 PMID: 20501857 DOI: 10.1158/0008-5472.CAN-10-0120
Source DB: PubMed Journal: Cancer Res ISSN: 0008-5472 Impact factor: 12.701