Altered expression of the septin gene, SEPT9, in ovarian neoplasia

被引:81
作者
Burrows, JF
Chanduloy, S
McIlhatton, MA
Nagar, H
Yeates, K
Donaghy, P
Price, J
Godwin, AK
Johnston, PG
Russell, SHE [1 ]
机构
[1] Queens Univ Belfast, Belfast City Hosp, Dept Oncol, Ctr Canc Res, Belfast BT9 7AB, Antrim, North Ireland
[2] Queens Univ Belfast, Belfast City Hosp, Dept Obstet & Gynaecol, Ctr Canc Res, Belfast BT9 7AB, Antrim, North Ireland
[3] Fox Chase Canc Ctr, Dept Med Oncol, Philadelphia, PA 19111 USA
关键词
alternative splicing; ovarian carcinoma; septin gene transcripts; methylation;
D O I
10.1002/path.1484
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The septin family of genes has been implicated in a variety of cellular processes including cytokinesis, membrane transport and fusion, exocytosis, and apoptosis. One member of the septin family maps to chromosome 17q25.3, a region commonly deleted in sporadic ovarian and breast tumours, and has also been identified as a fusion partner of MLL in acute myeloid leukaemias. The present study demonstrates that the pattern of expression of multiple splice variants of this septin gene is altered in ovarian tumours and cell lines. In particular, expression of the zeta transcript is detectable in the majority of tumours and cell lines, but not in a range of non-malignant adult and fetal tissues. Zeta expression is accompanied by loss of the ubiquitous beta transcript. Somatic mutations of the gene were not detected in ovarian tumours, but it was demonstrated that beta expression in tumour cell lines can be reactivated by 5-azacytidine treatment, suggesting a role for methylation in the control of expression of this gene. Copyright (C) 2003 John Wiley Sons, Ltd.
引用
收藏
页码:581 / 588
页数:8
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