Linking transcriptional elongation and messenger RNA export to metastatic breast cancers

被引:53
作者
Guo, SC
Hakimi, MA
Baillat, D
Chen, XW
Farber, MJ
Klein-Szanto, AJP
Cooch, NS
Godwin, AK
Shiekhattar, R
机构
[1] Wistar Inst Anat & Biol, Philadelphia, PA 19104 USA
[2] Fox Chase Canc Ctr, Dept Med Oncol, Philadelphia, PA 19111 USA
关键词
D O I
10.1158/0008-5472.CAN-04-3624
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The biochemical pathways that are disrupted in the genesis of sporadic breast cancers remain unclear. Moreover, the present prognosticating markers used to determine the prognosis of node-negative patient leads to probabilistic results, and the eventual clinical course is far from certain. Here we identified the human TREX complex, a multiprotein complex that links transcription elongation to mRNA transport, as culprit of aggressive human breast cancers. We show that whereas p84N5 (called hTREX84) is expressed at very low levels in normal breast epithelial cells, it is highly expressed in breast tumors. Importantly, hTREX84 expression correlates with tumor size and the metastatic state of the tumor progression. Reduction of hTREX84 levels in breast cancer cell lines by small interfering RNA result in inhibition of cellular proliferation and abrogation of rill export. These results not only identify hTREX84 as a prognosticator of breast cancer but also delineate human TREX complex as a target for therapeutic drugs against breast cancer.
引用
收藏
页码:3011 / 3016
页数:6
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