Kuroki T, Fujiwara Y, Tsuchiya E, Nakamori S, Imaoka S, Kanematsu T, Nakamura Y
Department of Biochemistry, Cancer Institute, Tokyo, Japan.
Genes Chromosomes Cancer. 1995 Jul;13(3):163-7. doi: 10.1002/gcc.2870130305.
To investigate cumulative genetic changes during development and progression of hepatocellular carcinoma (HCC), we examined DNAs isolated from 104 tumors for loss of heterozygosity (LOH) at 13 loci on six chromosomal arms and for an increase of copy number ("multiplication") of alleles on 8q, using polymorphic microsatellite markers. A comparison of genetic features with clinicopathological stages of these tumors revealed that LOH on 1p had occurred in tumors at an early stage or with a well-differentiated histological phenotype (8/26; 31%) as well as in tumors at more advanced stages. Genetic alterations on chromosome arms 4q, 8p, 8q, 13q, 16q, and 17p were more often observed in tumors of more advanced stages and poorer differentiation grades. When size was the criterion for comparison, LOH on 1p was observed frequently even in tumors smaller than 2 cm (6/16; 38%), whereas allelic losses on 16q were detected frequently only in larger tumors. These results suggest that the putative tumor suppressor gene(s) assumed to be located on 1p may be involved in an early step of carcinogenesis in liver tissue and that the other genetic alterations examined here may play important roles in progression of HCC.
为了研究肝细胞癌(HCC)发生发展过程中的累积基因变化,我们使用多态性微卫星标记,检测了从104个肿瘤中分离出的DNA,以分析6个染色体臂上13个位点的杂合性缺失(LOH),以及8号染色体上等位基因拷贝数的增加(“倍增”)。将这些肿瘤的基因特征与临床病理分期进行比较,结果显示,1号染色体短臂(1p)上的LOH出现在早期肿瘤或具有高分化组织学表型的肿瘤中(8/26;31%),也出现在更晚期的肿瘤中。4号染色体长臂(4q)、8号染色体短臂(8p)、8号染色体长臂(8q)、13号染色体长臂(13q)、16号染色体长臂(16q)和17号染色体短臂(17p)上的基因改变,在更晚期和低分化等级的肿瘤中更常出现。以肿瘤大小作为比较标准时,即使在小于2 cm的肿瘤中也经常观察到1p上的LOH(6/16;38%),而16q上的等位基因缺失仅在较大肿瘤中频繁检测到。这些结果表明,假定位于1p上的假定肿瘤抑制基因可能参与肝组织癌变的早期阶段,并且本文检测的其他基因改变可能在HCC的进展中起重要作用。