Comparative genomic hybridization reveals differences in DNA copy number changes between sporadic gastric carcinomas and gastric carcinomas from patients with hereditary nonpolyposis colorectal cancer

Cancer Genetics and Cytogenetics

Volumn 106, Issue 1, 1998, Pages 62-65

  Larramendy, Marcelo L ^a,b   El Rifai, Wa'el ^a,c   Kokkola, Arto ^d   Puolakkainen, Pauli ^d   Monni, Outi ^a   Salovaara, Reijo ^a   Aarnio, Markku ^d   Knuutila, Sakari ^a,d  

^a UNIVERSITY OF HELSINKI   (Finland)

^b FACULTAD DE CIENCIAS NATURALES Y MUSEO   (Argentina)

^c NATIONAL RESEARCH CENTRE   (Egypt)

^d HELSINKI UNIVERSITY CENTRAL HOSPITAL   (Finland)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CANCER GENETICS; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CLINICAL ARTICLE; COLORECTAL CANCER; DNA DETERMINATION; FEMALE; GENE AMPLIFICATION; GENE LOSS; HUMAN; HUMAN TISSUE; MALE; PRIORITY JOURNAL; STOMACH CARCINOMA;

CHROMOSOME ABERRATIONS; COLORECTAL NEOPLASMS; FEMALE; HUMANS; IMAGE PROCESSING, COMPUTER-ASSISTED; MALE; NUCLEIC ACID HYBRIDIZATION;

EID: 0032190838     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-4608(98)00046-6     Document Type: Article

References (22)

1. 1. Dunlop MG (1992): Screening for large bowel neoplasms in individuals with a family history of colorectal cancer. Br J Cancer 79:488-494.
2. 2. Aaltonen L, Peltomäki P, Leach FS, Sistonen P, Pylkkänen L, Mecklin J-P, Järvinen H, Powell SM, Jen J, Hamilton SR, Petersen GM, Kinzler KW, Vogelstein B, de la Chapelle A (1993): Clues to the pathogenesis of familial colorectal cancer. Science 260:812-816.
3. 3. Peltomäki P, Aaltonen L, Sistonen P, Pylkkänen L, Mecklin J-P, Järvinen H, Green JS, Jass JR, Weber JL, Leach FS, Petersen GM, Hamilton SR, de la Chapelle A, Vogelstein B (1993): Genetic mapping of a locus predisposing to human colorectal cancer. Science 260:810-812.
4. 4. Houltston RS, Collins A, Slack J, Morton NE (1992): Dominant genes for colorectal cancer are not rare. Ann Hum Genet 56:99-103.
5. 5. Cannon-Albright LA, Skolnick MH, Bishop DT, Lee RG, Burt RW (1988): Common inheritance of susceptibility to colonic adenomatous polyps and associated colorectal cancers. N Engl J Med 319:533-537.
6. 6. Mecklin J-P (1987): Frequency of hereditary colorectal cancer. Gastroenterology 93:1021-1025.
7. 7. Järvinen HJ (1992): Epidemiology of familial adenomatous polyposis in Finland: impact of family screening of the colorectal cancer rate and survival. Gut 33:357-360.
8. 8. Aaltonen L, Sankila R, Mecklin J-P, Järvinen H, Pukkala E, Peltomäki P, de la Chapelle A (1994): A novel approach to estimate the proportion of hereditary non-polyposis colorectal cancer of total colorectal cancer burden. Cancer Detect Prev 18:57-63.
9. 9. Heim S, Mitelman F (1995): Cancer Cytogenetics. ed 2, Wiley-Liss, New York.
10. 10. Tahara E (1995): Molecular biology of gastric cancer. World J Surg 19:484-490.
11. 11. Kokkola A, Monni O, Puolakkainen P, Larramendy ML, Victorzon M, Nordling S, Haapiainen R, Kivilaakso E, Knuutila S (1997): 17q12-21 amplicon, a novel recurrent genetic change in intestinal type of gastric carcinoma: a comparative genomic hybridization study. Genes Chromosom Cancer 20:1-6.
12. 12. Vasen HFA, Mecklin J-P, Meera Khan P, Lynch HT (1991): The international collaborative group on hereditary non-polyposis colorectal cancer (ICG-HNPCC). Dis Colon Rectum 34:424-425.
13. 13. Nyström-Lahti M, Wu Y, Moisio A, Hofstra R, Osinga J, Mecklin J, Järvinen H, Leisti J, Buys C, de la Chapelle A, Peltomäki P (1996): DNA mismatch repair gene mutation in 55 kindreds with verified or putative hereditary non-polyposis colorectal cancer. Hum Mol Genet 5:763-769.
14. 14. Miller SA, Dykes DD, Polesky HF (1988): A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res 16:1215.
15. 15. Kallioniemi O-P, Kallioniemi A, Piper J, Isola J, Waldman FM, Gray JW, Pinkel D (1994): Optimizing comparative genomic hybridization for analysis of DNA sequence copy number changes in solid tumors. Genes Chromosom Cancer 10:231-243.
16. 16. Larramendy ML, Tarkkanen M, Valle J, Kivioja AH, Ervasti H, Karaharju E, Salmivalli T, Elomaa I, Knuutila S (1997): Gains, losses, and amplifications of DNA sequences evaluated by comparative genomic hybridization in chondrosarcomas. Am J Pathol 150:685-691.
17. 17. Watson SA, Durrant LG, Crosbie JD, Morris DL (1989): The in vitro growth response of primary colorectal and gastric cancer cells to gastrin. Int J Cancer 43:692-696.
18. 18. Rakic S, Milicevic MN (1991): Serum gastrin levels in patients with intestinal and diffuse type of gastric cancer. Br J Cancer 64:1189.
19. 19. Tsugawa K, Fushida S, Yonemura Y (1993): Amplification of c-erbB2 gene in gastric carcinoma: correlation with survival. Oncology 50:418-425.
20. 20. Park J-B, Rhim JS, Park S-C, Kimm SW, Kraus M (1989): Amplification, overexpression, and rearrangement of the eroB-2 protooncogene in primary human stomach carcinomas. Cancer Res 49:6605-6609.
21. 21. Viel A, Genuardi M, Capozzi E, Leonardi F, Bellacosa A, Paravatou-Petsotas M, Pomponi M, Fornasarig M, Percesepe A, Roncucci L, Tamassia M, Benatti P, Ponz de Leon M, Valenti A, Covino M, Anti M, Foletto M, Boiocchi M, Neri G (1997): Characterization of MSH2 and MLH1 mutations in Italian families with hereditary nonpolyposis colorectal cancer. Genes Chromosom Cancer 18:8-18.
22. 22. Herfarth K, Kodner I, Whelan A, Ivanovich J, Bracamontes J, Wells S, Goodfellow P (1997): Mutations in MLH1 are more frequent than in MSH2 in sporadic colorectal cancers with microsatellite instability. Genes Chromosom Cancer 18:42-49.