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. 1999 Mar;79(7-8):1049–1052. doi: 10.1038/sj.bjc.6690168

Mutation analysis of the Fanconi anaemia A gene in breast tumours with loss of heterozygosity at 16q24.3

A-M Cleton-Jansen 1, E W Moerland 1, J C Pronk 2, C G M van Berkel 2, S Apostolou 3, J Crawford 3, A Savoia 4, A D Auerbach 5, C G Mathew 6, D F Callen 3, C J Cornelisse 1
PMCID: PMC2362253  PMID: 10098735

Abstract

The recently identified Fanconi anaemia A (FAA) gene is located on chromosomal band 16q24.3 within a region that has been frequently reported to show loss of heterozygosity (LOH) in breast cancer. FAA mutation analysis of 19 breast tumours with specific LOH at 16q24.3 was performed. Single-stranded conformational polymorphism (SSCP) analysis on cDNA and genomic DNA, and Southern blotting failed to identify any tumour-specific mutations. Five polymorphisms were identified, but frequencies of occurrence did not deviate from those in a normal control population. Therefore, the FAA gene is not the gene targeted by LOH at 16q24.3 in breast cancer. Another tumour suppressor gene in this chromosomal region remains to be identified. © 1999 Cancer Research Campaign

Keywords: Fanconi anaemia, breast cancer, allelic imbalance, tumour suppressor gene, chromosome 16

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Selected References

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  1. Berx G., Cleton-Jansen A. M., Nollet F., de Leeuw W. J., van de Vijver M., Cornelisse C., van Roy F. E-cadherin is a tumour/invasion suppressor gene mutated in human lobular breast cancers. EMBO J. 1995 Dec 15;14(24):6107–6115. doi: 10.1002/j.1460-2075.1995.tb00301.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Berx G., Cleton-Jansen A. M., Strumane K., de Leeuw W. J., Nollet F., van Roy F., Cornelisse C. E-cadherin is inactivated in a majority of invasive human lobular breast cancers by truncation mutations throughout its extracellular domain. Oncogene. 1996 Nov 7;13(9):1919–1925. [PubMed] [Google Scholar]
  3. Cher M. L., Ito T., Weidner N., Carroll P. R., Jensen R. H. Mapping of regions of physical deletion on chromosome 16q in prostate cancer cells by fluorescence in situ hybridization (FISH). J Urol. 1995 Jan;153(1):249–254. doi: 10.1097/00005392-199501000-00086. [DOI] [PubMed] [Google Scholar]
  4. Cleton-Jansen A. M., Moerland E. W., Kuipers-Dijkshoorn N. J., Callen D. F., Sutherland G. R., Hansen B., Devilee P., Cornelisse C. J. At least two different regions are involved in allelic imbalance on chromosome arm 16q in breast cancer. Genes Chromosomes Cancer. 1994 Feb;9(2):101–107. doi: 10.1002/gcc.2870090205. [DOI] [PubMed] [Google Scholar]
  5. Devilee P., van Vliet M., van Sloun P., Kuipers Dijkshoorn N., Hermans J., Pearson P. L., Cornelisse C. J. Allelotype of human breast carcinoma: a second major site for loss of heterozygosity is on chromosome 6q. Oncogene. 1991 Sep;6(9):1705–1711. [PubMed] [Google Scholar]
  6. Dorion-Bonnet F., Mautalen S., Hostein I., Longy M. Allelic imbalance study of 16q in human primary breast carcinomas using microsatellite markers. Genes Chromosomes Cancer. 1995 Nov;14(3):171–181. doi: 10.1002/gcc.2870140304. [DOI] [PubMed] [Google Scholar]
  7. Gschwend M., Levran O., Kruglyak L., Ranade K., Verlander P. C., Shen S., Faure S., Weissenbach J., Altay C., Lander E. S. A locus for Fanconi anemia on 16q determined by homozygosity mapping. Am J Hum Genet. 1996 Aug;59(2):377–384. [PMC free article] [PubMed] [Google Scholar]
  8. Ianzano L., D'Apolito M., Centra M., Savino M., Levran O., Auerbach A. D., Cleton-Jansen A. M., Doggett N. A., Pronk J. C., Tipping A. J. The genomic organization of the Fanconi anemia group A (FAA) gene. Genomics. 1997 May 1;41(3):309–314. doi: 10.1006/geno.1997.4675. [DOI] [PubMed] [Google Scholar]
  9. Iida A., Isobe R., Yoshimoto M., Kasumi F., Nakamura Y., Emi M. Localization of a breast cancer tumour-suppressor gene to a 3-cM interval within chromosomal region 16q22. Br J Cancer. 1997;75(2):264–267. doi: 10.1038/bjc.1997.43. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Latil A., Cussenot O., Fournier G., Driouch K., Lidereau R. Loss of heterozygosity at chromosome 16q in prostate adenocarcinoma: identification of three independent regions. Cancer Res. 1997 Mar 15;57(6):1058–1062. [PubMed] [Google Scholar]
  11. Lo Ten Foe J. R., Rooimans M. A., Bosnoyan-Collins L., Alon N., Wijker M., Parker L., Lightfoot J., Carreau M., Callen D. F., Savoia A. Expression cloning of a cDNA for the major Fanconi anaemia gene, FAA. Nat Genet. 1996 Nov;14(3):320–323. doi: 10.1038/ng1196-320. [DOI] [PubMed] [Google Scholar]
  12. Moerland E., Breuning M. H., Cornelisse C. J., Cleton-Jansen A. M. Exclusion of BBC1 and CMAR as candidate breast tumour-suppressor genes. Br J Cancer. 1997;76(12):1550–1553. doi: 10.1038/bjc.1997.594. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Patel K. J., Yu V. P., Lee H., Corcoran A., Thistlethwaite F. C., Evans M. J., Colledge W. H., Friedman L. S., Ponder B. A., Venkitaraman A. R. Involvement of Brca2 in DNA repair. Mol Cell. 1998 Feb;1(3):347–357. doi: 10.1016/s1097-2765(00)80035-0. [DOI] [PubMed] [Google Scholar]
  14. Pronk J. C., Gibson R. A., Savoia A., Wijker M., Morgan N. V., Melchionda S., Ford D., Temtamy S., Ortega J. J., Jansen S. Localisation of the Fanconi anaemia complementation group A gene to chromosome 16q24.3. Nat Genet. 1995 Nov;11(3):338–340. doi: 10.1038/ng1195-338. [DOI] [PubMed] [Google Scholar]
  15. Scully R., Chen J., Plug A., Xiao Y., Weaver D., Feunteun J., Ashley T., Livingston D. M. Association of BRCA1 with Rad51 in mitotic and meiotic cells. Cell. 1997 Jan 24;88(2):265–275. doi: 10.1016/s0092-8674(00)81847-4. [DOI] [PubMed] [Google Scholar]
  16. Skirnisdottir S., Eiriksdottir G., Baldursson T., Barkardottir R. B., Egilsson V., Ingvarrson S. High frequency of allelic imbalance at chromosome region 16q22-23 in human breast cancer: correlation with high PgR and low S phase. Int J Cancer. 1995 Apr 21;64(2):112–116. doi: 10.1002/ijc.2910640207. [DOI] [PubMed] [Google Scholar]
  17. Tsuda H., Callen D. F., Fukutomi T., Nakamura Y., Hirohashi S. Allele loss on chromosome 16q24.2-qter occurs frequently in breast cancers irrespectively of differences in phenotype and extent of spread. Cancer Res. 1994 Jan 15;54(2):513–517. [PubMed] [Google Scholar]

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