Lothe R A, Fosså S D, Stenwig A E, Nakamura Y, White R, Børresen A L, Brøgger A
Department of Genetics, Norwegian Radium Hospital, Montebello, Oslo.
Genomics. 1989 Jul;5(1):134-8. doi: 10.1016/0888-7543(89)90097-9.
Constitutional and tumor genotypes defined by polymorphic DNA markers were examined in 31 testicular cancer patients. Constitutional karyotypes were analyzed and clinical data presented. We analyzed 11 loci representing 8 chromosomes, including regions frequently deleted in other types of cancer. Loss of 3p or 11p sequences was detected in 8 of 28 heterozygotes (28%) and in 5 of 20 heterozygotes (25%). This gives a combined total loss of 40%. The other autosomal loci tested showed no loss or a loss of less than 10% of alleles. We suggest that this loss of heterozygosity for genetic material on chromosome 3p or on 11p is nonrandom and important in the development of a major subset of testicular neoplasms.
我们对31例睾丸癌患者的多态性DNA标记所定义的体质和肿瘤基因型进行了检测。分析了体质核型并给出了临床数据。我们分析了代表8条染色体的11个位点,包括其他类型癌症中经常缺失的区域。在28例杂合子中的8例(28%)以及20例杂合子中的5例(25%)检测到3p或11p序列缺失。这使得总缺失率达到40%。所检测的其他常染色体位点未显示缺失或等位基因缺失率低于10%。我们认为,3号染色体或11号染色体上遗传物质的这种杂合性缺失是非随机的,并且在一大类睾丸肿瘤的发生发展中具有重要意义。