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2003 | 50 | 1 |

Tytuł artykułu

Analysis of the G-C polymorphism in the 5'-untranslated region of the RAD51 gene in breast cancer

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
The breast cancer suppressor proteins BRCA1 and BRCA2 interact with RAD51, a protein essential for maintaining genomic stability by playing a central role in homology-dependent recombinational repair of the DNA double-strand breaks. Therefore, genetic variability in the RAD51 gene may contribute to the appearance and/or progression of breast cancer. A single nucleotide polymorphism in the 5 - un­translated region of RAD51 (a G to C substitution at position 135, the G/C polymor­phism) is reported to modulate breast cancer risk. We investigated the distribution of genotypes and frequency of alleles of the G/C polymorphism in breast cancer. Tumor tissues were obtained from postmenopausal women with node-negative and node-positive breast carcinoma with uniform tumor size. Blood samples from age matched healthy women served as control. The G/C polymorphism was determined by PCR-based MvaI restriction fragment length polymorphism. The distribution of the genotypes of the G/C polymorphism did not differ significantly (P > 0.05) from those predicted by the Hardy-Weinberg distribution. There were no differences in the geno­type distribution and allele frequencies between node-positive and node-negative pa­tients. There were no significant differences between distributions of the genotypes in subgroups assigned to histological grades according to Scarf–Bloom–Richardson criteria and the distribution predicted by Hardy–Weinberg equilibrium (P > 0.05). Our study implies that the G/C polymorphism of the RAD51 gene may not be directly involved in the development and/or progression of breast cancer and so it may not be useful as an independent marker in this disease.

Wydawca

-

Rocznik

Tom

50

Numer

1

Opis fizyczny

p.249-253,fig.

Twórcy

autor
  • University of Lodz, S.Banacha 12-16, 90-237 Lodz, Poland
autor
autor
autor
autor
autor

Bibliografia

  • Chen PL, Chen CF, Chen Y, Xiao J, Sharp ZD, Lee WH. (1998) Proc Natl Acad Sci U S A.; 95: 5287-92.
  • Gonzales R, Silva JM, Dominguez G, Garcia JM, Martinez G, Vargas J, Provencio M, Espana P, Bonilla F. (1999) Br J Cancer.; 81: 503-9.
  • Kute TE, Grondahl-Hansen J, Shao SM, Long M, Russel G, Brunner N. (1998) Breast Cancer Res Treat.; 47: 9-16.
  • Levy-Lahad E, Lahad A, Eisenberg S, Dagan E, Paperna T, Kasinetz L, Catane R, Kaufman B, Beller U, Renbaum P, Gershoni-Baruch R. (2001) Proc Natl Acad Sci US A.; 98: 3232-6.
  • Wang W, Tucker MA, Doody MM, Tarone RE, Struewing JP. (1999) Am J Hum Genet.; 655: 22 (abstract).
  • Wang WW, Spurdle A, Kolachana P, Bove B, Modan B, Ebbers SM, Suthers G, Tucker MA, Kaufman DJ, Doody MM, Tarone RE, Daly M, Levavi H, Pierce H, Chetrit A, Yechezkel GH, Chenevix-Trench G, Offit K, Godwin AK, Struewing JP. (2001) Cancer Epidemiol Biomarkers Prev.; 10: 955-60.
  • Welcsh PL, Owens KN, King MC. (2000) Trends Genet.; 16: 69-74.
  • Yoshikawa K, Ogawa T, Baer R, Hemmi H, Honda K, Yamauchi A, Inamoto T, Ko K, Yazumi S, Motoda H, Kodama H, Noguchi S, Gazdar AF, Yamaoka Y, Takahashi R. (2000) Int J Cancer.; 88: 28-36.

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

bwmeta1.element.agro-article-14e8b935-88a0-4577-b71b-3841aa9817ce
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