Eiriksdottir G, Johannesdottir G, Ingvarsson S, Björnsdottir I B, Jonasson J G, Agnarsson B A, Hallgrimsson J, Gudmundsson J, Egilsson V, Sigurdsson H, Barkardottir R B
Department of Pathology, University and National Hospital of Iceland, Reykjavik, Iceland.
Eur J Cancer. 1998 Dec;34(13):2076-81. doi: 10.1016/s0959-8049(98)00241-x.
Several chromosome regions exhibit loss of heterozygosity (LOH) in human breast carcinoma and are thought to harbour tumour suppressor genes (TSG). At chromosome 13q, two TSGs have been identified, RB1 at 13q14 and BRCA2 at 13q12-q13. In this study, 139 sporadic breast tumours were analysed with 18 polymorphic microsatellite markers for detailed mapping of LOH at chromosome 13q and evaluation of an association with known progression factors. LOH with at least one marker was observed in 71 (51%) of the tumours analysed. The deletion mapping indicated three LOH target regions, 13q12-q13, 13q14 and 13q31-q34. LOH at chromosome 13q12-q13 was associated with low progesterone receptor content, a high S phase fraction and aneuploidy. Multivariate analysis adjusting for lymph node involvement and S phase fraction showed that patients with tumours exhibiting LOH at 13q12-q13 have a 3-4-fold increased risk of recurrence and death compared with other patients. Our results suggest there are at least three separate LOH target regions at chromosome 13q and inactivation of one or more genes at chromosome 13q12-q13 results in poor prognosis for breast cancer patients.
在人类乳腺癌中,几个染色体区域表现出杂合性缺失(LOH),并且被认为含有肿瘤抑制基因(TSG)。在13号染色体长臂(13q)上,已鉴定出两个肿瘤抑制基因,位于13q14的RB1和位于13q12 - q13的BRCA2。在本研究中,使用18个多态性微卫星标记对139例散发性乳腺肿瘤进行分析,以详细绘制13q染色体上杂合性缺失图谱并评估其与已知进展因子的相关性。在所分析的肿瘤中,71例(51%)观察到至少一个标记的杂合性缺失。缺失图谱显示出三个杂合性缺失目标区域,即13q12 - q13、13q14和13q31 - q34。13q12 - q13染色体上的杂合性缺失与低孕激素受体含量、高S期分数和非整倍体相关。在对淋巴结受累情况和S期分数进行校正的多变量分析中,显示13q12 - q13处出现杂合性缺失肿瘤的患者与其他患者相比,复发和死亡风险增加3至4倍。我们的结果表明,13q染色体上至少存在三个独立的杂合性缺失目标区域,并且13q12 - q13染色体上一个或多个基因的失活会导致乳腺癌患者预后不良。