ST18 is a breast cancer tumor suppressor gene at human chromosome 8q11.2

被引:0
|
作者
Burkhard Jandrig
Susanne Seitz
Bernd Hinzmann
Wolfgang Arnold
Burkhard Micheel
Konrad Koelble
Reiner Siebert
Arnfried Schwartz
Karin Ruecker
Peter M Schlag
Siegfried Scherneck
André Rosenthal
机构
[1] Max-Delbrück-Centre for Molecular Medicine,Department of Tumor Genetics
[2] Signature diagnostics AG,undefined
[3] atugen AG,undefined
[4] Institute of Biochemistry and Biology,undefined
[5] University Potsdam,undefined
[6] Institute of Pathology,undefined
[7] Charité Hospital,undefined
[8] Humboldt University,undefined
[9] Clinic of Surgery and Surgical Oncology,undefined
[10] Robert Rössle Hospital,undefined
[11] Institute of Human Genetics,undefined
[12] University Hospital Schleswig-Holstein,undefined
[13] Campus Kiel,undefined
来源
Oncogene | 2004年 / 23卷
关键词
breast cancer; tumor suppressor genes; chromosome 8q11;
D O I
暂无
中图分类号
学科分类号
摘要
We have identified a gene, ST18 (suppression of tumorigenicity 18, breast carcinoma, zinc-finger protein), within a frequent imbalanced region of chromosome 8q11 as a breast cancer tumor suppressor gene. The ST18 gene encodes a zinc-finger DNA-binding protein with six fingers of the C2HC type (configuration Cys-X5-Cys-X12-His-X4-Cys) and an SMC domain. ST18 has the potential to act as transcriptional regulator. ST18 is expressed in a number of normal tissues including mammary epithelial cells although the level of expression is quite low. In breast cancer cell lines and the majority of primary breast tumors, ST18 mRNA is significantly downregulated. A 160 bp region within the promoter of the ST18 gene is hypermethylated in about 80% of the breast cancer samples and in the majority of breast cancer cell lines. The strong correlation between ST18 promoter hypermethylation and loss of ST18 expression in tumor cells suggests that this epigenetic mechanism is responsible for tumor-specific downregulation. We further show that ectopic ST18 expression in MCF-7 breast cancer cells strongly inhibits colony formation in soft agar and the formation of tumors in a xenograft mouse model.
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页码:9295 / 9302
页数:7
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