| Literature DB >> 25036127 |
Koshiki Mino1, Satoshi Nishimura, Shogo Ninomiya, Hiroshi Tujii, Yasumasa Matsumori, Mie Tsuchida, Miho Hosoi, Koichi Koseki, Shuichi Wada, Makoto Hasegawa, Ryuzo Sasaki, Yukie Murakami-Yamaguchi, Hiroshi Narita, Takayoshi Suzuki, Naoki Miyata, Tamio Mizukami.
Abstract
Tissue factor pathway inhibitor-2 (TFPI-2) is a major inhibitor of extracellular matrix degradation. Decreases in TFPI-2 contribute to malignant tumor cell production, and TFPI-2 is a presumed tumor suppressor. TFPI-2 gene transcription is regulated by two epigenetic mechanisms: DNA methylation of the promoter and K4 methylation of histone 3 (H3). Lysine-specific demethylase 1 (LSD1) and LSD2 demethylate H3K4me2/1. LSD1 has been implicated in TFPI-2 regulation through both epigenetic mechanisms, but the involvement of LSD2 remains unknown. We prepared a monoclonal anti-LSD2 antibody that clearly distinguishes LSD2 from LSD1. Knockdown of LSD1 or LSD2 by siRNAs increased TFPI-2 protein and mRNA. Simultaneous knockdown of both LSD1 and LSD2 showed additive effects. Bisulfite sequencing revealed that CpG sites in the TFPI-2 promoter region were unmethylated. These results indicate that LSD2 also contributes to TFPI-2 regulation through histone modification, and that further studies of the involvement of LSD2 in tumor malignancy are warranted.Entities:
Keywords: histone H3K4 methylation; lysine-specific demethylases (LSD1 and LSD2); monoclonal anti-LSD2 antibody; tissue factor pathway inhibitor-2 (TFPI-2)
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Year: 2014 PMID: 25036127 DOI: 10.1080/09168451.2014.910104
Source DB: PubMed Journal: Biosci Biotechnol Biochem ISSN: 0916-8451 Impact factor: 2.043