Herbst R A, Weiss J, Ehnis A, Cavenee W K, Arden K C
Ludwig Institute for Cancer Research, La Jolla, California 92093-0660.
Cancer Res. 1994 Jun 15;54(12):3111-4.
Karyotypic and molecular data indicate that genetic events involving the chromosome region 10q22-10qter may be related to tumorigenesis in malignant melanoma. To test this we analyzed 10 polymorphic microsatellite repeats in the region 10q22-qter, using a polymerase chain reaction-based assay for loss of heterozygosity and DNA isolated from normal and tumor tissue from 26 individuals with malignant melanoma. The samples included 19 paired normal and malignant tissues representing various stages of melanoma as well as 7 cases in which samples from at least 2 different points in time during tumor progression were available. Our findings indicate that loss of heterozygosity of 10q22-10qter is a frequent event, that the observed loss of heterozygosity does not result from whole chromosome loss, and that it is associated with tumor progression. Finally, the appearance of new alleles in two of the tumors may indicate the involvement of DNA replication errors in melanoma analogous to such events in other tumor types.
核型和分子数据表明,涉及染色体区域10q22 - 10qter的遗传事件可能与恶性黑色素瘤的肿瘤发生有关。为了验证这一点,我们使用基于聚合酶链反应的杂合性缺失检测方法,对26例恶性黑色素瘤患者的正常组织和肿瘤组织中分离的DNA,分析了10q22 - qter区域的10个多态性微卫星重复序列。样本包括19对代表黑色素瘤不同阶段的正常组织和恶性组织,以及7例在肿瘤进展过程中可获得至少两个不同时间点样本的病例。我们的研究结果表明,10q22 - 10qter的杂合性缺失是一个常见事件,观察到的杂合性缺失并非由整条染色体丢失所致,并且它与肿瘤进展相关。最后,两个肿瘤中出现新等位基因可能表明黑色素瘤中存在DNA复制错误,类似于其他肿瘤类型中的此类事件。