文献库 文献相关信息

题目:
Point mutations and genomic deletions in CCND1 create stable truncated cyclin D1 mRNAs that are associated with increased proliferation rate and shorter survival.
作者:
Wiestner(Adrian),Tehrani(Mahsa),Chiorazzi(Michael),Wright(George),Gibellini(Federica),Nakayama(Kazutaka),Liu(Hui),Rosenwald(Andreas),Muller-Hermelink(H Konrad),Ott(German),Chan(Wing C),Greiner(Timothy C),Weisenburger(Dennis D),Vose(Julie),Armitage(James O),Gascoyne(Randy D),Connors(Joseph M),Campo(Elias),Montserrat(Emilio),Bosch(Francesc),Smeland(Erlend B),Kvaloy(Stein),Holte(Harald),Delabie(Jan),Fisher(Richard I),Grogan(Thomas M),Miller(Thomas P),Wilson(Wyndham H),Jaffe(Elaine S),Staudt(Louis M)
状态:
发布时间2007-05-24 , 更新时间 2016-10-19
期刊:
Blood
摘要:
A gene expression signature of tumor proliferation rate in mantle cell lymphoma (MCL) is an overriding molecular predictor of the length of survival following diagnosis. Many strongly proliferative MCL tumors have exceptionally high cyclin D1 mRNA levels and preferentially express short cyclin D1 mRNA isoforms. We demonstrate here that these short mRNAs are cyclin D1a isoforms with truncated 3'UTRs, not alternatively spliced cyclin D1b mRNA isoforms. Among 15 MCL tumors with truncated cyclin D1 mRNAs, 7 had genomic deletions in the CCND1 3'UTR region. In 3 others, CCND1 contained point mutations that created premature polyadenylation signals, giving rise to 1.5-kb mRNAs lacking most of the 3'UTR. Both types of genomic alteration created transcripts lacking mRNA destabilization elements present in the wild-type cyclin D1a mRNA. Premature polyadenylation due to a 3'UTR mutation also was present in the Z-138 MCL cell line, which expressed both truncated and full-length cyclin D1a mRNAs. In these cells, the half-life of the short cyclin D1a mRNA was much longer than that of the full-length mRNA. We conclude that alterations of CCND1 3'UTR structure can significantly increase its oncogenic effect and worsen the clinical course of MCL patients.
语言:
eng
DOI:

联系方式

山东省济南市 高新区 崇华路359号 三庆世纪财富中心C1115室

电话: 0531-88819269

E-mail: product@genelibs.com

微信公众号

关注微信订阅号,实时查看信息,关注医学生物学动态。