Loss of heterozygosity in the region including the BRCA1 gene on 17q in colon cancer

Cancer Genetics and Cytogenetics

Volumn 104, Issue 2, 1998, Pages 119-123

  Garcia Patiño, Elena ^a   Gomendio, Blanca ^a   Lleonart, Matilde ^a   Silva, Jose M ^a   Garcia, Jose M ^a   Provencio, Mariano ^a   Cubedo, Ricardo ^a   España, Pilar ^a   Y Cajal, Santiago Ramón ^a   Bonilla, Félix ^a  

^a HOSPITAL UNIVERSITARIO PUERTA DE HIERRO   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

BRCA1 PROTEIN;

ALLELE; ARTICLE; BREAST CARCINOMA; CANCER RISK; CHROMOSOME 17Q; COLON CARCINOMA; GENE LOCUS; GENETIC SUSCEPTIBILITY; HETEROZYGOSITY LOSS; HUMAN; HUMAN TISSUE; MAJOR CLINICAL STUDY; PRIORITY JOURNAL; TUMOR SUPPRESSOR GENE;

BASE SEQUENCE; CHROMOSOMES, HUMAN, PAIR 17; COLONIC NEOPLASMS; DNA PRIMERS; GENES, BRCA1; HUMANS; LOSS OF HETEROZYGOSITY;

EID: 0032527873     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-4608(97)00460-3     Document Type: Article

References (32)

1. Astrin S.M., Costanzi C. The molecular genetics of colon cancer. Sem Oncol. 16:1989;138-147.
2. Silverberg E., Boring C.E., Squires T.S. Cancer statistics. CA-Cancer J Clin. 40:1990;9-26.
3. Fearon E.R., Vogelstein B. A genetic model for colorectal tumorigenesis. Cell. 61:1990;759-767.
4. Thibodeau S.N., Bren G., Schaid D. Microsatellite instability in cancer of the proximal colon. Science. 260:1993;816-819.
5. Aaltonen L.A., Peltomaki P., Leach F.S., Sistonen P., Pylkkänen L., Mecklin J.-P., Järvinen H., Powell S.M., Jen J., Hamilton S.R., Petersen G.M., Kinzler K.W., Vogelstein B., de la Chapelle A. Clues to the pathogenesis of familial colorectal cancer. Science. 260:1993;812-816.
6. Ionov Y., Peinado M.A., Malkhosyan S., Shibata D., Perucho M. Ubiquitous somatic mutations in simple repeated sequences reveal a new mechanism for colonic carcinogenesis. Nature. 363:1993;558-561.
7. Vogelstein B., Fearon E.R., Hamilton S.R., Kern S.E., Preisinger A.C., Leppert M., Nakumura Y., White R., Smits A.M.M., Bos J.L. Genetic alterations during colorectal-tumor development. N Engl J Med. 319:1988;525-532.
8. Delattre O., Olschwang S., Law D.J., Melot T., Remvikos Y., Salmon R.J., Sastre X., Validire P., Feimberg A.P., Thomas G. Multiple genetic alterations in distal and proximal colorectal cancer. Lancet. 2:1989;353-355.
9. Vogelstein B., Fearon E.R., Kern S.E., Hamilton S.R., Preisinger A.C., Nakamura Y., White R. Allelotype of colorectal carcinoma. Science. 244:1989;207-211.
10. Kinzler K.W., Nilbert M.C., Su L.-K. Identification of FAP locus genes from chromosome 5q21. Science. 252:1991;661-665.
11. Baker S.J., Fearon E.R., Nigro J.M., Hamilton S.R., Preisinger A.C., Jessup J.M., vanTunin P., Ledbetter D.H., Barker D.F., Nakamura Y., White R., Vogelstein B. Chromosome 17 deletions and p53 gene mutations in colorectal carcinomas. Science. 244:1989;217-221.
12. Fearon E.R., Cho K.R., Nigro J.M., Kern S.E., Simons J.W., Ruppert J.M., Hamilton S.R., Preisinger A.C., Thomas G., Kinzler K.W., Vogelstein B. Identification of a chromosome 18q gene that is altered in colorectal carcinoma. Science. 247:1990;49-56.
13. Offerhaus G.J.A., de Feyter E.P., Cornelisse C.J. The relationship of DNA aneuploidy to molecular genetic alterations in colorectal carcinoma. Gastroenterology. 102:1992;1612-1619.
14. Porter D.E., Cohen B.B., Wallace M.R., Smyth E., Chetty U., Dixon M., Steel C.M., Carter D.C. Breast cancer incidence, penetrance and survival in probable carriers of BRCA1 gene mutation in families linked to BRCA1 on chromosome 17q12-21. Br J Surg. 81:1994;1512-1515.
15. Ford D, Easton DF, Bishop DT, Narod SA, Goldgar DE, and the Breast Cancer Linkage Consortium (1994): Risks of cancer in BRCA1-mutation carriers. Lancet 343:692-695.
16. Cropp C.S., Nevanlinna H.A., Pyrhonen S., Stenman U.-H., Salmikangas P., Albertsen H., White R., Callahan R. Evidence for involvement of BRCA1 in sporadic breast carcinoma. Cancer Res. 54:1994;2548-2551.
17. Gao X., Zacharek A., Salkowski A., Grignon D.J., Sakr W., Porter A.T., Honn K.V. Loss of heterozygosity of the BRCA1 and other loci on chromosome 17q in human prostate cancer. Cancer Res. 55:1995;1002-1005.
18. Gao X., Zacharek A., Grignon D.J., Sark W., Powell I.J., Porter A.T., Honn K.V. Localization of potential tumor suppressor loci to a <2 Mb region on chromosome 17q in human prostate cancer. Oncogene. 11:1995;1241-1247.
19. Asler V.B., Coller F.A. The prognostic significance of direct extension of carcinoma of the colon and rectum. Ann Surg. 139:1954;76-90.
20. Oto M., Miyake S., Yuasa Y. Optimization of nonradioisotopic single strand conformation polymorphism analysis with a conventional minislab gel electrophoresis apparatus. Ann Biochem. 213:1993;19-22.
21. Miki Y., Swensen J., Shattuck-Eidens D., Futreal P.A., Harshman K., Tautigian S., Liu Q., Cochran C., Bennett L.M., Ding W., Bell R., Rosenthal J., Hussey C., Tran T., McClure M., Frye C., Hattier T., Phelps R., Haugen-Strano A., Katcher H., Yakumo K., Gholami Z., Shaffer D., Stone S., Bayer S., Wray C., Bogden R., Dayananth P., Ward J., Tonin P., Narod S., Bristow P.K., Norris F.H., Helvering L., Morrison P., Rosteck P., Lai M., Barret J.C., Lewis C., Neuhausen S., Cannon-Albright L., Goldgar D., Wiseman R., Kamb A., Skolnick M.H. A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1. Science. 266:1994;66-71.
22. Neuhausen S.L., Mazoyer S., Friedman L. Haplotype and phenotype analysis of six recurrent BRCA1 mutations in 61 families. results of an international study Am J Hum Genet. 58:1996;271-280.
23. Hall F.M., Lee M.L., Newman B., Morrow J.E., Anderson L.A., Huey B., King M.-C. Linkage of early-onset familial breast cancer to chromosome 17q21. Science. 250:1990;1684-1689.
24. Castilla L.H., Couch F.J., Erdos M.R., Hoskins K.F., Calzone K., Garber J.E., Boyd J., Lubin M.B., Deshano M.L., Brody L.C., Collins F.S., Weber B.L. Mutations in the BRCA1 gene in families with early-onset breast and ovarian cancer. Nat Genet. 8:1994;387-391.
25. Baker S.J., Markowitz S., Fearon E.R., Willson J.K.V., Vogelstein B. Suppression of human colorectal carcinoma cell growth by wild-type p53. Science. 249:1990;217-221.
26. Hollstein M., Sidransky D., Vogelstein B., Harris C.C. p53 mutations in human cancers. Science. 253:1991;49-53.
27. Leggett B., Young J., Buttenshaw R. Colorectal carcinomas show frequent allelic loss on the long arm of chromosome 17 with evidence for a specific target region. Br J Cancer. 71:1995;1070-1073.
28. Campo E., Miquel R., Jares P., Bosch F., Juan M., Leone A., Vives J., Cardesa A., Yague J. Prognostic significance of the loss of heterozygosity of NM23-H1 and p53 genes in human colorectal carcinomas. Cancer. 73:1994;2913-2921.
29. Bardi G., Sukhikh T., Pandis N., Fenger C., Kronborg O., Heims S. Karyotypic characterization of colorectal adenocarcinomas. Genes Chromosom Cancer. 12:1995;97-109.
30. Lothe R.A., Andersen S.N., Hofstad B., Meling G.I., Peltomaki P., Heim S., Bregger A., Vatn M., Rognum T.O., Brresen A.L. Deletion of 1p loci and microsatellite instability in colorectal polyps. Genes Chromosom Cancer. 14:1995;182-188.
31. Mori T., Aoki T., Matsubara T., Iida F., Xi Qun D., Nishihira T., Mori S., Nakamura Y. Frequent loss of heterozygosity in the region including BRCA1 on chromosome 17q in squamous cell carcinomas of the esophagus. Cancer Res. 54:1994;1638-1640.
32. Peltomaki P., Aaltonen L.A., Sistonen P., Pylkkänen L., Mecklin J.-K., Järvinen H., Green J.S., Jass J.R., Weber J.L., Leach F.S., Petersen G.M., Hamilton S.R., de la Chapelle A., Vogelstein B. Genetic mapping of a locus predisposing to human colorectal cancer. Science. 260:1993;810-812.