Soukupova Jana, Dundr Pavel, Kleibl Zdenek, Pohlreich Petr
Department of Biochemistry and Experimental Oncology, First Faculty of Medicine, Charles University, Prague, Czech Republic.
Oncol Rep. 2008 Jun;19(6):1505-10.
Mutations in the ATM gene are the cause of a rare autosomal recessive syndrome, ataxia-telangiectasia (AT). Of the general population, approximately 0.35-1% has been estimated to be heterozygous for a germline mutation in the ATM gene. The finding that ATM heterozygotes have an increased breast cancer risk was supported by some studies but not confirmed by others. In our study, the entire coding sequence of the ATM gene was prescreened for mutations by the protein truncation test to detect the chain-terminating mutations that are highly predominant in patients with AT. DNA sequencing then characterized 3 (1.9%) pathogenic mutations among 161 high-risk breast cancer patients. The c.5177+1G>A splicing mutation was a novel gene alteration. No mutation was detected in a group of 183 control individuals. Our results suggest that truncating mutations in ATM increase breast cancer risk and contribute to inherited breast cancer. The analysis further uncovered the c.1066-6T>G splicing mutation once among high-risk patients (0.6%) and twice among controls (1.1%) suggesting that this mutation does not confer an increase in breast cancer risk. On the other hand, individuals heterozygous for this truncating variant displayed loss of exon 11 in approximately 50% of ATM transcripts. Immunohistochemistry did not detect the ATM protein in the tumor sample carrying this mutation. Thus, the association of the c.1066-6T>G mutation with familial breast cancer remains uncertain. Loss of the wild-type ATM allele has not been detected in the tumor samples from heterozygous carriers of the ATM mutation. Our experiments did not detect the hypermethylation of the ATM promoter in any of the DNA samples from tumor tissues.
ATM基因的突变是一种罕见的常染色体隐性综合征——共济失调毛细血管扩张症(AT)的病因。据估计,在普通人群中,约0.35 - 1%为ATM基因种系突变的杂合子。一些研究支持ATM杂合子患乳腺癌风险增加这一发现,但其他研究未予证实。在我们的研究中,通过蛋白质截短试验对ATM基因的整个编码序列进行突变预筛查,以检测在AT患者中高度常见的链终止突变。随后的DNA测序在161例高危乳腺癌患者中鉴定出3个(1.9%)致病性突变。c.5177 + 1G>A剪接突变是一种新的基因改变。在一组183名对照个体中未检测到突变。我们的结果表明,ATM基因的截短突变会增加乳腺癌风险,并导致遗传性乳腺癌。分析还发现,高危患者中曾有1例(0.6%)出现c.1066 - 6T>G剪接突变,对照中有2例(1.1%)出现该突变,这表明该突变不会增加乳腺癌风险。另一方面,这种截短变异的杂合子个体中,约50%的ATM转录本缺失外显子11。免疫组化未在携带该突变的肿瘤样本中检测到ATM蛋白。因此,c.1066 - 6T>G突变与家族性乳腺癌的关联仍不确定。在ATM突变杂合携带者的肿瘤样本中未检测到野生型ATM等位基因的缺失。我们的实验在任何肿瘤组织的DNA样本中均未检测到ATM启动子的高甲基化。