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常见 ATM 基因多态性与双侧乳腺癌的关联。

Association of common ATM polymorphism with bilateral breast cancer.

作者信息

Heikkinen Katri, Rapakko Katrin, Karppinen Sanna-Maria, Erkko Hannele, Nieminen Pentti, Winqvist Robert

机构信息

Department of Clinical Genetics, Oulu University Hospital, University of Oulu, Oulu, Finland.

出版信息

Int J Cancer. 2005 Aug 10;116(1):69-72. doi: 10.1002/ijc.20996.

Abstract

The ATM kinase has an essential role in maintaining genomic integrity. Loss of both ATM alleles results in ataxia-telangiectasia (A-T), a rare autosomal recessive neuroimmunologic disorder associated with cancer susceptibility. Individuals heterozygous for germline ATM mutations have been reported to have an increased risk for malignancy, in particular, female breast cancer. In the current study, a full mutation analysis of the ATM gene was carried out in patients from 121 breast or breast-ovarian cancer families. We discovered that the combination of 5557G-->A in cis position with IVS38-8 T-->C was associated with bilateral breast cancer (OR = 10.2; 95% CI = 3.1-33.8; p = 0.001). As the 5557G-->A change has been reported to affect an exonic splicing enhancer, we hypothesized that the observed composite allele could have some effect on the correct splicing of exon 39. However, no aberrant transcripts were detected, but ATM expression levels of lymphoblast cell lines from heterozygous carriers of this combination allele were lower than from noncarriers (p = 0.09). Lowered gene expression levels may have direct influence on the activities in DNA damage recognition and response pathways, as well as other genome integrity maintenance functions. Based on the results, we propose a cancer risk-modifying effect for the ATM 5557G-->A, IVS38-8T-->C composite allele.

摘要

ATM激酶在维持基因组完整性方面发挥着重要作用。ATM两个等位基因的缺失会导致共济失调毛细血管扩张症(A-T),这是一种罕见的常染色体隐性神经免疫疾病,与癌症易感性相关。据报道,携带种系ATM突变的杂合个体患恶性肿瘤的风险增加,尤其是女性乳腺癌。在本研究中,对来自121个乳腺癌或乳腺-卵巢癌家族的患者进行了ATM基因的全面突变分析。我们发现,顺式位置的5557G→A与IVS38-8 T→C的组合与双侧乳腺癌相关(OR = 10.2;95% CI = 3.1-33.8;p = 0.001)。由于据报道5557G→A的变化会影响外显子剪接增强子,我们推测观察到的复合等位基因可能对外显子39的正确剪接有一定影响。然而,未检测到异常转录本,但该组合等位基因杂合携带者的淋巴母细胞系的ATM表达水平低于非携带者(p = 0.09)。基因表达水平降低可能直接影响DNA损伤识别和反应途径以及其他基因组完整性维持功能的活性。基于这些结果,我们提出ATM 5557G→A、IVS38-8T→C复合等位基因具有癌症风险修饰作用。

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