Wu Yuanfei, Renard Claire-Angélique, Apiou Françoise, Huerre Michel, Tiollais Pierre, Dutrillaux Bernard, Buendia Marie Annick
Unité de Recombinaison et Expression Génétique (Inserm U163), Institut Pasteur, 28 rue du Dr. Roux, 75015 Paris, France.
Oncogene. 2002 Feb 28;21(10):1518-26. doi: 10.1038/sj.onc.1205208.
Transgenic mice expressing the c-Myc oncogene driven by woodchuck hepatitis virus (WHV) regulatory sequences develop hepatocellular carcinoma with a high frequency. To investigate genetic lesions that cooperate with Myc in liver carcinogenesis, we conducted a genome-wide scan for loss of heterozygosity (LOH) and mutational analysis of beta-catenin in 37 hepatocellular adenomas and carcinomas from C57BL/6 x castaneus F1 transgenic mice. In a subset of these tumors, chromosome imbalances were examined by comparative genomic hybridization (CGH). Allelotyping with 99 microsatellite markers spanning all autosomes revealed allelic imbalances at one or more chromosomes in 83.8% of cases. The overall fractional allelic loss was rather low, with a mean index of 0.066. However, significant LOH rates involved chromosomes 4 (21.6% of tumors), 14, 9 and 1 (11 to 16%). Interstitial LOH on chromosome 4 was mapped at band C4-C7 that contains the INK4a/ARF and INK4b loci, and on chromosome 14 at band B-D including the RB locus. In man, the homologous chromosomal regions 9p21, 13q14 and 8p21-23 are frequently deleted in liver cancer. LOH at chromosomes 1 and 14, and beta-catenin mutations (12.5% of cases) were seen only in HCCs. All tumors examined were found to be aneuploid. CGH analysis of 10 representative cases revealed recurrent gains at chromosomes 16 and 19, but losses or deletions involving mostly chromosomes 4 and 14 generally prevailed over gains. Thus, Myc activation in the liver might select for inactivation of tumor suppressor genes on regions of chromosomes 4 and 14 in a context of low genomic instability. Myc transgenic mice provide a useful model for better defining crosstalks between oncogene and tumor suppressor pathways in liver tumorigenesis.
由土拨鼠肝炎病毒(WHV)调控序列驱动表达c-Myc癌基因的转基因小鼠会高频发生肝细胞癌。为了研究在肝癌发生过程中与Myc协同作用的基因损伤,我们对37例来自C57BL/6×栗色鼠F1转基因小鼠的肝细胞腺瘤和癌进行了全基因组杂合性缺失(LOH)扫描以及β-连环蛋白的突变分析。在这些肿瘤的一个亚组中,通过比较基因组杂交(CGH)检查了染色体失衡情况。使用覆盖所有常染色体的99个微卫星标记进行等位基因分型显示,83.8%的病例在一条或多条染色体上存在等位基因失衡。总体等位基因缺失分数相当低,平均指数为0.066。然而,显著的LOH率涉及4号染色体(21.6%的肿瘤)、14号、9号和1号染色体(11%至16%)。4号染色体上的间质LOH定位在包含INK4a/ARF和INK4b基因座的C4-C7带,14号染色体上的间质LOH定位在包括RB基因座的B-D带。在人类中,同源染色体区域9p21、13q14和8p21-23在肝癌中经常缺失。1号和14号染色体上的LOH以及β-连环蛋白突变(12.5%的病例)仅在肝癌中出现。所有检查的肿瘤均为非整倍体。对10例代表性病例的CGH分析显示,16号和19号染色体出现反复增加,但涉及4号和14号染色体的缺失或缺失通常比增加更为普遍。因此,肝脏中的Myc激活可能在低基因组不稳定性的背景下选择4号和14号染色体区域的肿瘤抑制基因失活。Myc转基因小鼠为更好地定义肝癌发生过程中癌基因与肿瘤抑制途径之间的相互作用提供了一个有用的模型。