Ueda Naoki, Shiraha Hidenori, Fujikawa Tatsuya, Takaoka Nobuyuki, Nakanishi Yutaka, Suzuki Mayumi, Matsuo Noriyuki, Tanaka Shigetomi, Nishina Shin-Ichi, Uemura Masayuki, Takaki Akinobu, Shiratori Yasushi, Yamamoto Kazuhide
Department of Gastroenterology and Hepatology, Okayama University Graduate School of Medicine and Dentistry, 2-5-1 Shikata-cho, Okayama 700-8558, Japan.
Mol Oncol. 2008 Oct;2(3):241-9. doi: 10.1016/j.molonc.2008.06.004. Epub 2008 Jun 20.
Using GGCX gene-specific real-time PCR, exon 2 deletion splice variant of vitamin K-dependent gamma-glutamyl carboxylase (GGCX) mRNA was identified in HCC cell lines. Expressions of wild type and exon 2 deletion variant of GGCX were analyzed with relevance to DCP production in HCC cell lines. Hep3B, HepG2, HuH1, HuH7, and PLC/PRF/5 produced DCP, while SK-Hep-1, HLE, HLF, and JHH1 produced no detectable level of DCP. DCP-producing cells expressed exon 2 deletion variant of GGCX mRNA and protein, while DCP-negative cells expressed no detectable level of exon 2 deletion variant of GGCX. These results suggest that exon 2 deletion splice variant of GGCX causes dysfunction of GGCX enzyme activity resulting in DCP production in HCC cell lines.
利用GGCX基因特异性实时PCR技术,在肝癌细胞系中鉴定出维生素K依赖性γ-谷氨酰羧化酶(GGCX)mRNA的外显子2缺失剪接变体。分析了GGCX野生型和外显子2缺失变体的表达与肝癌细胞系中异常凝血酶原(DCP)产生的相关性。Hep3B、HepG2、HuH1、HuH7和PLC/PRF/5产生DCP,而SK-Hep-1、HLE、HLF和JHH1未检测到可检测水平的DCP。产生DCP的细胞表达GGCX mRNA和蛋白的外显子2缺失变体,而DCP阴性细胞未检测到GGCX外显子2缺失变体的可检测水平。这些结果表明,GGCX的外显子2缺失剪接变体导致GGCX酶活性功能障碍,从而导致肝癌细胞系中产生DCP。