High incidence of familial breast cancer segregates with constitutional t(11;22)(q23;q11)

Genes Chromosomes and Cancer

Volumn 45, Issue 10, 2006, Pages 945-949

  Wieland, Ilse ^a   Muschke, Petra ^a   Volleth, Marianne ^a   Röpke, Albrecht ^a   Pelz, Antje Friederike ^a   Stumm, Markus ^a,b   Wieacker, Peter ^a  

^a OTTO VON GUERICKE UNIVERSITY   (Germany)

^b Praxis für Ultraschall und Humangenetik ^*  (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGED; ARTICLE; BRAIN TUMOR; BREAST; BREAST CANCER; BREAST CARCINOGENESIS; BREAST TUMOR; CHROMOSOME TRANSLOCATION 11; CHROMOSOME TRANSLOCATION 22; CLINICAL ARTICLE; CONTROLLED STUDY; FAMILIAL CANCER; FEMALE; GENE DELETION; GENE SEGREGATION; GENETIC PREDISPOSITION; GLIOBLASTOMA; HETEROZYGOSITY LOSS; HUMAN; POLYMERASE CHAIN REACTION; POSTMENOPAUSE; PRIORITY JOURNAL;

ADULT; AGED; BRAIN NEOPLASMS; BREAST NEOPLASMS; CHROMOSOMES, HUMAN, PAIR 11; CHROMOSOMES, HUMAN, PAIR 22; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INCIDENCE; MALE; MIDDLE AGED; PEDIGREE; POLYMERASE CHAIN REACTION; TRANSLOCATION, GENETIC;

EID: 33748501700     PISSN: 10452257     EISSN: 10982264     Source Type: Journal    
DOI: 10.1002/gcc.20358     Document Type: Article

References (22)

1. Böhm M, Kleine-Besten R, Wieland I. 2000. Loss of heterozygosity on chromosome 5p defines 5p13-12 as the critical region involved in tumor progression of bladder carcinomas. Int J Cancer 89:194-197.
2. Collaborative Group on Hormonal Factors in Breast Cancer. 2001. Familial breast cancer: Collaborative reanalysis of individual data from 52 epidemiological studies including 58,209 women with breast cancer and 101,986 women without the disease. Lancet 358:1389-1399.
3. de Jong MM, Nolte IM, te Meerman GJ, van der Graaf WTA, Oosterwijk JC, Kleibeuker JH, Schaapveld M, de Vries EGE. 2002. Genes other than BRCA1 and BRCA2 involved in breast cancer susceptibility. J Med Genet 39:225-242.
4. de Stahl TD, Hartmann C, de Bustos C, Piotrowski A, Benetkiewicz M, Mantripragada KK, Tykwinski T, von Deimling A, Dumanski JP. 2005. Chromosme 22 tiling-path array-CGH analysis identifies germ-line and tumor-specific aberrations in patients with glioblastoma multiforme. Genes Chromosomes Cancer 44:161-169.
5. Dumitrescu RG, Cotarla I. 2005. Understanding breast cancer risk-Where do we stand in 2005? J Cell Mol Med 9:208-221.
6. Edelmann L, Spiteri E, Koren K, Pulijaal V, Bialer MG, Shanske A, Goldberg R, Morrow BE. 2001. AT-rich palindromes mediate the constitutional t(11;22) translocation. Am J Hum Genet 68:1-13.
7. Edelmann L, Spiteri E, McCain N, Goldberg R, Pandita RK, Duong S, Fox J, Blumenthal D, Lalani SR, Shaffer LG, Morrow BE. 1999. A common breakpoint on 11q23 in carriers of the constitutional t(11;22) translocation. Am J Hum Genet 65:1608-1616.
8. Hill AS, Foot NJ, Chaplin TL, Young BD. 2000. The most frequent constitutional translocation in humans, the t(11;22)(q23;q11) is due to a highly specific Alu-mediated recombination. Hum Mol Genet 9:1525-1532.
9. ISCN. 1995. An International System for Human Cytogenetic Nomenclature. In: Mitelman F, editor. Basel: Karger.
10. Iselius L, Lindsten J, Aurias A, Fraccaro M, Bastard C, Bottelli AM, Bui T-H, Caufin D, Dalprà N, Dutrillaux B, Fukushima Y, Geraedts JPM, De Grouchy J, Gyftodimou J, Hanley AL, Hansmann I, Ishii T, Jalbert P, Jingeleski S, Kajii T, von Koskull H, Niikawa N, Noel B, Pasquali F, Probeck HD, Robinson A, Roncarati E, Sachs E, Scappaticci S, Schwinger E, Simoni G, Veenema H, Vigi V, Volpato S, Wegner R-D, Welch JP, Winsor EJT, Zhang S, Zuffardi O. 1983. The 11;22q translocation: A collaborative study of 20 new cases and analysis of 110 families. Hum Genet 64:343-355.
11. James LA, Mitchell EL, Menasce L, Varley JM, 1997. Comperative genomic hybridization of ductual carcinoma in situ of the breast: Identification of regions of DNA amplification and deletion in common with invasive breast carcinoma. Oncogene 14:1059-1065.
12. Jobanputra V, Chung WK, Hacker AM, Emanuel BS, Warburton D. 2005. A unique case of der(11)t(11;22),-22 arising from 3:1 segregation of a maternal t(11;22) in a family with co-segregation of the translocation and breast cancer. Prenat Diagn 25:683-686.
13. Kurahashi H, Emanuel BS. 2001a. Long AT-rich palindromes and the constitutional t(11;22) breakpoint. Hum Mol Genet 10:2605-2617.
14. Kurahashi H, Emanuel BS. 2001b. Unexpectedly high rate of de novo constitutional t(11;22) translocations in sperm from normal males. Nat Genet 29:139-140.
15. Kurahashi H, Shaikh TH, Zackai EH, Celle L, Driscoll DA, Budarf ML, Emanuel BS. 2000. Tightly clustered 11 q23 and 22q11 breakpoints permit PCR-based detection of recurrent constitutional t(11;22). Am J Hum Genet 67:763-768.
16. Lindblom A, Sandelin K, Iselius L, Dumanski J, White I, Nordenskjöld M, Larsson C. 1994. Predisposition for breast cancer in carriers of constitutional translocation 11q;22q. Am J Hum Genet 54:871-876.
17. Martin ES, Cesari R, Pentimalli F, Yoder K, Fishel R, Himelstein AL, Martin SE, Godwin AK, Negrini M, Croce CM. 2003. The BCSC-1 locus at chromosome 11q23-q24 is a candidate tumor suppressor gene. Proc Natl Acad Sci USA 100:11517-11522.
18. Oldenburg RA, Kroeze-Jansema K, Meijers-Heijboer H, van Asperen CJ, Hoogerbrugge N, van Leeuwen I, Vasen HFA, Cleton-Jansen A-M, Kraan J, Houwing-Duistermaat JJ, Morreau H, Cornelisse CJ, Devilee P. 2006. Characterization of familial non-BRCA1/2 breast tumors by loss of heterozygosity and immunophenotyping. Clin Cancer Res 12:1693-1700.
19. Röpke A, Buhtz P, Böhm M, Seger J, Wieland I, Allhoff EP, Wieacker PF 2005, Promoter CpG hypermethylation and downregulation of DICE1 expression in prostate cancer. Oncogene 24:6667-6675.
20. Shaikh TH, Budarf ML, Celle L, Zackai EH, Emanuel BS. 1999. Clustered 11q23 and 22q11 breakpoints and 3:1 meiotic malsegregation in multiple unrelated t(11;22) families. Am J Hum Genet 65:1595-1607.
21. Tapia-Páez I, O'Brien KP, Kost-Alimova M, Sahlén S, Kedra D, Bruder CE, Andersson B, Roe BA, Hu P, Imreh S, Blennow E, Dumanski JP. 2000. Fine mapping of the constitutional translocation t(11;22)(q23;q11). Hum Genet 106:506-516.
22. Zackai EH, Emanuel BS. 1980. Site-specific reciprocal translocation, t(11;22)(q23;q11), in several unrelated families with 3:1 meiotic disjunction. Am J Med Genet 7:507-521.