Krylova Nadezhda Yu, Lobeiko Oksana S, Sokolenko Anna P, Iyevleva Aglaya G, Rozanov Maxim E, Mitiushkina Natalia V, Gergova Madina M, Porhanova Tatiana V, Urmancheyeva Adel F, Maximov Sergey Ya, Togo Alexandr V, Imyanitov Evgeny N
NN Petrov Institute of Oncology, St, Petersburg, Russia; Medical Academy of Postgraduate Studies, St, Petersburg, Russia.
Hered Cancer Clin Pract. 2006 Sep 15;4(4):193-6. doi: 10.1186/1897-4287-4-4-193.
The BRCA1 4153delA allele is frequently referred to as the Russian founder mutation, as it was initially detected in several cancer families from Moscow. Our earlier studies have demonstrated 1% occurrence of BRCA1 4153delA heterozygosity in familial and/or early-onset and/or bilateral Russian breast cancer (BC) patients. Since literature data suggest that the 4153delA variant is more associated with ovarian cancer (OC) than with BC, we expected to reveal a highly elevated frequency of this genotype in Russian ovarian cancer series. However, real-time allele-specific PCR genotyping has detected only two BRCA1 4153delA carriers out of 177 unselected OC patients (1.1%). Both these carriers were early-onset and had serous carcinomas of grade 3. Thus, our study supports neither the Russian origin of BRCA1 4153delA mutation, nor its selectivity towards ovarian versus breast cancer predisposition.
BRCA1基因4153delA等位基因常被称为俄罗斯始祖突变,因为它最初是在来自莫斯科的几个癌症家族中被检测到的。我们早期的研究表明,在俄罗斯家族性和/或早发性和/或双侧乳腺癌(BC)患者中,BRCA1基因4153delA杂合性的发生率为1%。由于文献数据表明,4153delA变异与卵巢癌(OC)的相关性高于与乳腺癌的相关性,我们预计在俄罗斯卵巢癌系列中会发现这种基因型的频率大幅升高。然而,实时等位基因特异性PCR基因分型在177例未经选择的OC患者中仅检测到2例BRCA1基因4153delA携带者(1.1%)。这两名携带者均为早发性,患有3级浆液性癌。因此,我们的研究既不支持BRCA1基因4153delA突变起源于俄罗斯,也不支持其对卵巢癌与乳腺癌易感性的选择性。