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Open Access Research article

Tissue factor pathway inhibitor-2 was repressed by CpG hypermethylation through inhibition of KLF6 binding in highly invasive breast cancer cells

Hongshen Guo1, Yifeng Lin2, Hongwei Zhang3, Juan Liu3, Nong Zhang2, Yiming Li4, Desheng Kong1, Qiqun Tang1 and Duan Ma1*

Author Affiliations

1 Key Laboratory of Molecular Medicine, Ministry of Education, Yixueyuan Road 138#, Shanghai Medical College, Fudan University, Shanghai 200032, China

2 Department of Pathology, Shanghai Medical College, Yixueyuan Road 138#, Fudan University, Shanghai 200032, China

3 Department of Surgery, Zhongshan Hospital, Fenglin Road 180#, Fudan University Shanghai 200032, China

4 Department of endocrinology, Huashan Hospital, Wulumuqi Middle Road 12#, Fudan University Shanghai 200032, China

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BMC Molecular Biology 2007, 8:110  doi:10.1186/1471-2199-8-110

Published: 3 December 2007

Abstract

Background

Tissue factor pathway inhibitor-2 (TFPI-2) is a matrix-associated Kunitz inhibitor that inhibits plasmin and trypsin-mediated activation of zymogen matrix metalloproteinases involved in tumor progression, invasion and metastasis. Here, we have investigated the mechanism of DNA methylation on the repression of TFPI-2 in breast cancer cell lines.

Results

We found that both protein and mRNA of TFPI-2 could not be detected in highly invasive breast cancer cell line MDA-MB-435. To further investigate the mechanism of TFPI-2 repression in breast cancer cells, 1.5 Kb TFPI-2 promoter was cloned, and several genetic variations were detected, but the promoter luciferase activities were not affected by the point mutation in the promoter region and the phenomena was further supported by deleted mutation. Scan mutation and informatics analysis identified a potential KLF6 binding site in TFPI-2 promoter. It was revealed, by bisulfite modified sequence, that the CpG island in TFPI-2 promoter region was hypermethylated in MDA-MB-435. Finally, using EMSA and ChIP assay, we demonstrated that the CpG methylation in the binding site of KLF-6 diminished the binding of KLF6 to TFPI-2 promoter.

Conclusion

In this study, we found that the CpG islands in TFPI-2 promoter was hypermethylated in highly invasive breast cancer cell line, and DNA methylation in the entire promoter region caused TFPI-2 repression by inducing inactive chromatin structure and decreasing KLF6 binding to its DNA binding sequence.