Yamamoto Y, Sakamoto M, Fujii G, Kanetaka K, Asaka M, Hirohashi S
Pathology Division, National Cancer Center Research Institute, Tokyo, Japan.
Clin Cancer Res. 2001 Feb;7(2):297-303.
Few genes related to carcinogenesis and progression of hepatocellular carcinoma (HCC) have been identified to date. In the present study, we report the cloning and characterization of a novel gene, DRH1, which is frequently down-regulated in HCC. The full-length DRH1 clone contains an open reading frame of 1257 nucleotides encoding 419 amino acids. The deduced DRH1 protein shows 41% identity to VDUP1, expression of which is rapidly induced by 1,25-dihydroxyvitamin D3. The DRH1 gene was localized to chromosome 15, and DRH1 protein was mainly observed in the cytoplasm of transiently transfected cells. Real-time quantitative reverse transcription-PCR analysis showed that the expression level of DRH1 was reduced in 29 of 35 (83%) HCCs compared with corresponding noncancerous liver tissue. The average (mean +/- SE) ratio of DRH1 expression level in tumor to corresponding noncancerous tissue was significantly different between well, moderately, and poorly differentiated HCCs (1.15 +/- 0.23, 0.69 +/- 0.10, and 0.19 +/- 0.04, respectively) and between HCCs without and with vascular invasion (0.94 +/- 0.16 and 0.46 +/- 0.07, respectively). These results indicate that the down-regulation of DRH1 occurs not at an early stage but rather at a late stage of HCC progression. Although the function of DRH1 protein is still unknown, our findings suggest that DRH1 is related to the progression of HCC and may provide a new prognostic factor.
迄今为止,很少有与肝细胞癌(HCC)发生和进展相关的基因被鉴定出来。在本研究中,我们报告了一个新基因DRH1的克隆和特性,该基因在HCC中经常下调。全长DRH1克隆包含一个1257个核苷酸的开放阅读框,编码419个氨基酸。推导的DRH1蛋白与VDUP1有41%的同源性,VDUP1的表达可被1,25 - 二羟基维生素D3快速诱导。DRH1基因定位于15号染色体,DRH1蛋白主要在瞬时转染细胞的细胞质中观察到。实时定量逆转录 - PCR分析表明,与相应的癌旁肝组织相比,35例HCC中有29例(83%)的DRH1表达水平降低。在高分化、中分化和低分化HCC之间(分别为1.15±0.23、0.69±0.10和0.19±0.04)以及在无血管侵犯和有血管侵犯的HCC之间(分别为0.94±0.16和0.46±0.07),肿瘤中DRH1表达水平与相应癌旁组织的平均(均值±标准误)比值有显著差异。这些结果表明,DRH1的下调并非发生在HCC进展的早期,而是晚期。尽管DRH1蛋白的功能仍然未知,但我们的发现表明DRH1与HCC的进展相关,可能提供一个新的预后因素。