BRCA1 4153delA founder mutation in Russian ovarian cancer patients

نویسندگان

  • Nadezhda Yu Krylova
  • Oksana S Lobeiko
  • Anna P Sokolenko
  • Aglaya G Iyevleva
  • Maxim E Rozanov
  • Natalia V Mitiushkina
  • Madina M Gergova
  • Tatiana V Porhanova
  • Adel F Urmancheyeva
  • Sergey Ya Maximov
  • Alexandr V Togo
  • Evgeny N Imyanitov
چکیده

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.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

High frequency of BRCA1, but not CHEK2 or NBS1 (NBN), founder mutations in Russian ovarian cancer patients

BACKGROUND A significant portion of ovarian cancer (OC) cases is caused by germ-line mutations in BRCA1 or BRCA2 genes. BRCA testing is cheap in populations with founder effect and therefore recommended for all patients with OC diagnosis. Recurrent mutations constitute the vast majority of BRCA defects in Russia, however their impact in OC morbidity has not been yet systematically studied. Furt...

متن کامل

Hereditary Breast Cancer in Latvia: Mutation Analysis of the BRCA1 Gene

Breast cancer is the main cause of death from malignant diseases in Latvian women. However, there have been no data concerning hereditary breast cancer from this region so far. Mutation screening of the breast cancer susceptibility genes BRCA1 and BRCA2 in high-risk Hungarian and Russian breast/ovarian cancer families indicated that founder effects of both genes in Central and Eastern Europe ar...

متن کامل

BRCA1 founder mutations do not contribute to increased risk of gastric cancer in the Polish population

BACKGROUND Gastric cancer (GC) is part of the spectrum of diseases linked to BRCA1 and BRCA2 mutations that increase the risk of breast and ovarian cancer. Data suggesting an increased risk of developing GC among BRCA1 and BRCA2 mutation carriers are based almost exclusively on indirect studies. The objective was to assess in a direct study whether there is a relationship between GC and selecte...

متن کامل

Clinical features and outcomes of germline mutation BRCA1-linked versus sporadic ovarian cancer patients

BACKGROUND The role of germline mutations in BRCA1 and BRCA2 genes in the risk of the development of ovarian cancer is clinically well established. BRCA1/2 testing seems to have increasing role in clinical management in patients with advanced ovarian cancer who require treatment with poly(ADP-ribose) polymerase inhibitors. METHODS Between 2002 - 2008, 125 consecutive patients with ovarian can...

متن کامل

Cancer risks in first degree relatives of BRCA1 mutation carriers: effects of mutation and proband disease status.

BACKGROUND Mutations in the BRCA1 (MIM 113705) gene are found in many families with multiple cases of breast and ovarian cancer, and women with a BRCA1 mutation are at significantly higher risk of developing breast and ovarian cancer than are the general public. METHODS We obtained blood samples and pedigree information from 3568 unselected cases of early-onset breast cancer and 609 unselecte...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره 4  شماره 

صفحات  -

تاریخ انتشار 2006