Fujiwara Y, Emi M, Ohata H, Kato Y, Nakajima T, Mori T, Nakamura Y
Department of Biochemistry, Cancer Institute, Tokyo, Japan.
Cancer Res. 1993 Mar 1;53(5):1172-4.
We have examined loss of heterozygosity on the short arm of chromosome 8 in 133 colorectal carcinomas, using 20 restriction fragment length polymorphism markers. Loss of heterozygosity was observed in 58 (44%) of 131 tumors that were informative with at least one locus. Among these 58, 32 revealed a partial or interstitial deletion of chromosome 8p. Detailed deletion mapping of chromosome 8p in these tumors identified two distinct, commonly deleted regions. One was located between markers C18-266 and pSVL-LPL at 8p23.2-8p22, and the other between CI8-319 and CI8-494 at 8p21.3-8p11.22. The genetic lengths of these two intervals were estimated to be 28 and 18 cM, respectively. The results suggest that at least two tumor suppressor genes associated with colorectal carcinomas are present on chromosome 8p. Correlation of loss of heterozygosity on 8p to the clinicopathological stage was also detected, suggesting that inactivation of a tumor suppressor gene(s) on 8p plays a role in progression of colorectal carcinomas.
我们使用20个限制性片段长度多态性标记,检测了133例结肠直肠癌中8号染色体短臂上杂合性缺失的情况。在131例至少有一个位点具有信息性的肿瘤中,58例(44%)观察到杂合性缺失。在这58例中,32例显示8号染色体短臂存在部分或中间缺失。对这些肿瘤中8号染色体短臂进行详细的缺失定位,确定了两个不同的常见缺失区域。一个位于8p23.2 - 8p22的标记C18 - 266和pSVL - LPL之间,另一个位于8p21.3 - 8p11.22的CI8 - 319和CI8 - 494之间。这两个区间的遗传长度估计分别为28和18厘摩。结果表明,8号染色体短臂上至少存在两个与结肠直肠癌相关的肿瘤抑制基因。还检测到8号染色体短臂杂合性缺失与临床病理分期的相关性,提示8号染色体短臂上一个或多个肿瘤抑制基因的失活在结肠直肠癌进展中起作用。