Devilee P, Hermans J, Eyfjörd J, Bøorresen A L, Lidereau R, Sobol H, Borg A, Cleton-Jansen A M, Oláh E, Cohen B B, Scherneck S, Hamann U, Peterlin B, Caligo M, Bignon Y J, Maugard C
Department of Human Genetics, University of Leiden, The Netherlands.
Genes Chromosomes Cancer. 1997 Mar;18(3):193-9.
Loss of heterozygosity (LOH) at 7q31 has been claimed to occur in over 80% of all breast cancers and to be of prognostic significance. This would make this genetic alteration the most common event observed in breast cancer to date. Others, however, have been unable to confirm this high incidence. In this multicenter study, we have complied LOH scorings for three polymorphic markers for 7q31-q32 in 683 breast tumors. Although some significant differences between centers existed, no center reported more than 40% LOH, and the average rate was 19%. Disease-free and overall survival of the patients whose tumors carried LOH at 7q31 did not differ significantly from those patients whose tumors showed retention of heterozygosity at 7q31. In a double-blind scoring of a subset of the raw data, an average discordant rate of LOH scoring of 12% was observed. While startling in itself, this was unable to explain the variation among centers, nor the difference with the initially reported high rate of LOH. We conclude that LOH at 7q31 is not important as a genetic alteration in breast cancer as originally suggested, nor a strong determinant of disease outcome.
7号染色体长臂31区(7q31)杂合性缺失(LOH)据称在超过80%的乳腺癌中发生,且具有预后意义。这将使这种基因改变成为迄今为止在乳腺癌中观察到的最常见事件。然而,其他人无法证实这种高发生率。在这项多中心研究中,我们对683例乳腺肿瘤的7q31 - q32区域的三个多态性标记进行了LOH评分。虽然各中心之间存在一些显著差异,但没有一个中心报告的LOH超过40%,平均发生率为19%。肿瘤在7q31发生LOH的患者的无病生存期和总生存期与肿瘤在7q31显示杂合性保留的患者相比,没有显著差异。在对一部分原始数据进行双盲评分时,观察到LOH评分的平均不一致率为12%。虽然这本身令人吃惊,但它无法解释各中心之间的差异,也无法解释与最初报道的高LOH发生率之间的差异。我们得出结论,7q31的LOH并不像最初所认为的那样,作为乳腺癌中的一种基因改变很重要,也不是疾病预后的一个强决定因素。