Experimental and Molecular Medicine (Dec 2018)

Whole genome MBD-seq and RRBS analyses reveal that hypermethylation of gastrointestinal hormone receptors is associated with gastric carcinogenesis

  • Hee-Jin Kim,
  • Tae-Wook Kang,
  • Keeok Haam,
  • Mirang Kim,
  • Seon-Kyu Kim,
  • Seon-Young Kim,
  • Sang-Il Lee,
  • Kyu-Sang Song,
  • Hyun-Yong Jeong,
  • Yong Sung Kim

DOI
https://doi.org/10.1038/s12276-018-0179-x
Journal volume & issue
Vol. 50, no. 12
pp. 1 – 14

Abstract

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Stomach cancer: DNA methylation of hormone receptor genes A sequencing study reveals abnormal changes to DNA that set the stage for stomach cancer development. DNA methylation, the addition of methyl groups to alter DNA activity, is often disrupted in human cancers. Yong Sung Kim at the Korea Research Institute of Bioscience and Biotechnology (KRIBB) in Daejeon, South Korea, and co-workers used sequencing technogy to identify critical methylation changes in stomach epithelial cells, intestinal metaplasia lesion and tumor cells during early-stage gastric cancer. The team found 3,035 abnormally methylated DNA regions related to the expression of particular genes. Further analysis identified six hormone receptor genes directly involved with stomach acid secretion, whose altered expression was linked to over-methylated DNA regions. Loss of function within these six genes may lead to gastric cancer, and their expression levels could be valuable biomarkers for the disease.