Chinen K, Isomura M, Izawa K, Fujiwara Y, Ohata H, Iwamasa T, Nakamura Y
Laboratory of Molecular Medicine, University of Tokyo, Japan.
Cytogenet Cell Genet. 1996;75(2-3):190-6. doi: 10.1159/000134480.
The loss of heterozygosity that is frequently observed at chromosome 8p22-->p21.3 in hepatocellular carcinomas (HCC), colorectal cancers (CRC), prostate cancers (PRC). and non-small cell lung cancers (NSCLC), suggests the presence there of one or more tumor suppressor genes associated with development and/or progression of these types of carcinomas. We have constructed a cosmid contig map of the target region by means of Southern hybridization and have isolated 45 exon-like fragments by exon amplification, using cosmid clones derived from three yeast artificial chromosomes (YACs). The map and the exon-like fragments reported here will be useful resources for isolation of the putative tumor suppressor gene(s) as well as other novel genes located in the 8p22-->p21.3 region.
在肝细胞癌(HCC)、结直肠癌(CRC)、前列腺癌(PRC)和非小细胞肺癌(NSCLC)中,经常在染色体8p22→p21.3区域观察到杂合性缺失,这表明该区域存在一个或多个与这些类型癌症的发生和/或进展相关的肿瘤抑制基因。我们通过Southern杂交构建了目标区域的粘粒重叠群图谱,并使用来自三个酵母人工染色体(YAC)的粘粒克隆,通过外显子扩增分离出45个外显子样片段。本文报道的图谱和外显子样片段将为分离推定的肿瘤抑制基因以及位于8p22→p21.3区域的其他新基因提供有用的资源。