Hypermethylation leads to bone morphogenetic protein 6 downregulation in hepatocellular carcinoma

PLoS One. 2014 Jan 30;9(1):e87994. doi: 10.1371/journal.pone.0087994. eCollection 2014.

Abstract

Background: In the liver, bone morphogenetic protein 6 (BMP-6) maintains balanced iron metabolism. However, the mechanism that underlies greater BMP-6 expression in hepatocellular carcinoma (HCC) tissue than adjacent non-cancerous tissue is unclear. This study sought to investigate the epigenetic mechanisms of BMP-6 expression by analysing the relationship between the DNA methylation status of BMP-6 and the expression of BMP-6.

Methods: Methylation-specific polymerase chain reaction (PCR), bisulphite sequencing PCR, the MethyLight assay, and quantitative real-time PCR were performed to examine BMP-6 methylation and mRNA expression levels. Immunohistochemistry (IHC) was performed on tissue arrays to evaluate the BMP-6 protein level.

Results: BMP-6 mRNA expression was approximately 84.09% lower in HCC tissues than in adjacent non-cancerous tissues, and this low level of expression was associated with a poor prognosis. Moreover, the hypermethylation observed in HCC cell lines and HCC tissues was correlated with the BMP-6 mRNA expression level, and this correlation was validated following treatment with 5-aza-CdR, a demethylation agent. In addition, BMP-6 DNA methylation was upregulated by 68.42% in 114 clinical HCC tissue samples compared to adjacent normal tissues, whereas the BMP-6 staining intensity was downregulated by 77.03% in 75 clinical HCC tissue samples in comparison to adjacent normal tissues. Furthermore, elevated expression of BMP-6 in HCC cell lines inhibited cell colony formation.

Conclusions: Our results suggest that BMP-6 CpG island hypermethylation leads to decreased BMP-6 expression in HCC tissues.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bone Morphogenetic Protein 6 / genetics*
  • Carcinoma, Hepatocellular / genetics*
  • Carcinoma, Hepatocellular / pathology
  • Cell Line, Tumor
  • CpG Islands / genetics
  • DNA Methylation / genetics*
  • Down-Regulation / genetics*
  • Gene Expression Regulation, Neoplastic / genetics
  • Humans
  • Liver / pathology
  • Liver Neoplasms / genetics*
  • Liver Neoplasms / pathology
  • Prognosis
  • Promoter Regions, Genetic / genetics
  • RNA, Messenger / genetics
  • Up-Regulation / genetics

Substances

  • BMP6 protein, human
  • Bone Morphogenetic Protein 6
  • RNA, Messenger

Grants and funding

This work was supported by the Natural Science Foundation of the Shanghai Science and Technology Committee (No. 12ZR1430200), the research fund of the State Key Laboratory of Oncogenes and Related Genes (91-11-05), and the Young Scientists Foundation of the Shanghai Cancer Institute (SB11-10). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.