转移酶
肝细胞癌
癌变
甘氨酸
生物
酶
生物化学
分子生物学
基因
氨基酸
酰基转移酶
化学
癌症研究
作者
Moe Matsuo,Kensuke Terai,Noriaki Kameda,Aya Matsumoto,Yumiko Kurokawa,Yuichi Funase,Kazuko Nishikawa,Naoki Sugaya,Nobuyuki Hiruta,Toshihiko Kishimoto
标识
DOI:10.1016/j.bbrc.2012.03.099
摘要
The human glycine-N-acyltransferase (hGLYAT) gene and two related-genes (GLYATL1 and GLYATL2) were isolated. Human GLYAT, GLYATL1, and GLYATL2 cDNAs were isolated and shown to encode polypeptides of 295, 302, and 294 amino acids, respectively. GLYAT catalyzes glycine-N-acyltransfer reaction with benzoyl-CoA acting as a typical aralkyl transferase, while GLYATL1 catalyzed glutamine-N-acyltransfer reaction with phenylacetyl-CoA as an arylacetyl transferase. GLYAT was shown to be expressed specifically in the liver and kidney, and the cellular localization of GLYAT protein was restricted to the mitochondria. Interestingly, labeling using highly affinity purified anti-GLYAT antibody revealed that GLYAT expression was suppressed in all hepatocellular carcinomas, but not in other liver diseases. hGLYAT repression in cancerous cells in the liver was controlled at the transcriptional level. hGLYAT is a good candidate as a novel marker of hepatocellular carcinoma and may be a key molecule in the transition between differentiation and carcinogenesis of liver cells.
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