Mapping of chromosomal imbalances in pancreatic carcinoma by comparative genomic hybridization

Cancer Research

Volumn 56, Issue 16, 1996, Pages 3803-3807

  Solinas Toldo, Sabina ^b   Wallrapp, Christine ^c   Müller Pillasch, Friedericke ^c   Bentz, Martin ^a,b   Gress, Thomas ^c   Lichter, Peter ^b  

^a UNIVERSITY OF HEIDELBERG   (Germany)

^b GERMAN CANCER RESEARCH CENTER DKFZ   (Germany)

^c UNIVERSITY HOSPITAL ULM   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ARTICLE; CHROMOSOME 16P; CHROMOSOME 17Q; CHROMOSOME 20Q; CHROMOSOME 22Q; CHROMOSOME 9P; CHROMOSOME ABERRATION; CHROMOSOME MAP; CONTROLLED STUDY; DNA HYBRIDIZATION; FEMALE; HUMAN; HUMAN TISSUE; IMAGE ANALYSIS; MALE; METAPHASE; ONCOGENE; PANCREAS CARCINOMA; PRIORITY JOURNAL; TUMOR SUPPRESSOR GENE;

ADENOCARCINOMA; CHROMOSOME ABERRATIONS; CHROMOSOME MAPPING; FEMALE; GENES, TUMOR SUPPRESSOR; HUMANS; MALE; NUCLEIC ACID HYBRIDIZATION; PANCREATIC NEOPLASMS; PROTO-ONCOGENES;

EID: 0029761612     PISSN: 00085472     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (29)

1. Gordis, L., and Gold, E. B. Epidemiology and etiology of pancreatic cancer. In: V L. W Go, E P Di Magno, J D. Gardner, E. Lebenthal, H. A. Reber, and G. A. Scheele (eds), The Pancreas: Biology, Pathobiology and Disease, 2nd ed , pp 837-855. New York. Raven Press, 1993.
2. Murr, M M., Starr, M. G , Oishi, A. J , and van Heerden, J. A. Pancreatic cancer. CA Cancer J Clin., 44: 304-318, 1994.
3. Myers, M H , and Gloecker-Riess, L A Cancer patients survival rates SEER programme for 10 years of follow-up CA Cancer J. Clin , 39: 21-32, 1989.
4. Casalone, R , Meriggi, F., Form, E., and Pasquali, F. Cytogenetic findings in a case of anaplastic carcinoma of the pancreas Cancer Genet Cytogenet, 29 253-259, 1987.
5. Johansson, B , Bardi, G , Heim, S , Mandahl, N , Mertens, F., Bak-Jensen, E., Andrén-Sandberg, A., and Mitelman, F Nonrandom chromosomal rearrangements in pancreatic carcinomas. Cancer (Phila ), 09: 1674-1681, 1992
6. Bardi, G , Johansson, B , Pandis, N , Mandahl, N., Bak-Jensen, E , Andrén-Sandberg, A., Mitelman, F., and Heim, S Karyotypic abnormalities in tumours of the pancreas Br J. Cancer, 67: 1106-1112, 1993.
7. Griffin, C. A., Hruban, R H , Long, P. P , Morsberger, L. A., Douna-Issa, F., and Yeo, C J Chromosome abnormalities in pancreatic adenocarcinoma Genes Chromosomes & Cancer, 9: 93-100, 1994.
8. Long, P. P., Hruban, R. H , Lo, R., Yeo, C. J., Morsberger, L A , and Griffin, C. A. Chromosome analysis of nine endocrine neoplasms of the pancreas Cancer Genet. Cytogenet, 77: 55-59, 1994.
9. Griffin, C. A., Hruban, R. H , Morsberger, L. A., Ellingham, T., Long, P. P., Jaffee, E M., Hauda, K. M , Bohlander, S. K., and Yeo, C. J Consistent abnormalities in adenocarcinoma of the pancreas. Cancer Res., 55: 2394-2399, 1995.
10. Kallioniemi, A , Kallioniemi, O-P., Sudan D , Rutovitz, D , Gray, J. W., Waldman, F., and Pinkel, D. Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors. Science (Washington DC), 258: 818-821, 1992.
11. du Manoir, S., Speicher, M. R., Joos, S., Schrock, E., Popp, S., Dohner, H., Kovacs, G., Robert-Nicoud, M., Lichter, P., and Cremer, T. Detection of complete and partial chromosome gains and losses by comparative genomic in situ hybridization. Hum. Genet , 90, 590-610, 1993.
12. Joos, S , Scherthan, H., Speicher, M. R , Schlegel, J., Cremer, T., and Lichter, P. Detection of amplified DNA sequences by reverse chromosome painting using genomic tumor DNA as probe Hum. Genet , 90; 584-589, 1993.
13. Hermanek, P., and Sobin, L H. (eds.) TNM Classification of Malignant Tumours, 4th ed, 2nd revision, pp. 71-73. Berlin: Springer-Verlag, 1992
14. Sambrook, J., Fritsch, E F., and Maniatis, T. (eds.) Molecular Cloning: A Laboratory Manual, 2nd ed, pp. 7.19-7.22 Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press, 1989
15. Lichter, P , Bentz, M , du Manoir, S , and Joos, S. Comparative genomic hybridization In. R. S Verma and A Babu (eds.), Human Chromosomes, pp 191-210. New York. McGraw-Hill, 1995
16. du Manoir, S., Schrock, E., Bentz, M , Speicher, M. R., Joos, S., Ried, T., Lichter, P., and Cremer, T. Quantitative analysis of comparative genomic hybridization. Cytometry, 19: 27-41, 1995.
17. Bentz, M., Dohner, H , Huck, K., Schutz, B., Ganser, A., Joos, S., du Manoir, S., and Lichter, P Comparative genomic hybridization in the investigation of myeloid leukemias Genes Chromosomes & Cancer, 72: 193-200, 1995
18. Schröck, E., Thiel, G , Lozanova, T., du Manoir, S., Meffert, M. C., Jauch, A , Speicher, M. R., Nürnberg, P., Vogel, S., Janisch, W , Donis-Keller, H., Ried, T., Witkowski, R., and Cremer, T. Comparative genomic hybridization of human malignant gliomas reveals multiple amplification sites and nonrandom chromosomal gains and losses. Am. J Pathol., 144: 1203-1218, 1994.
19. Bentz, M., Huck, K., du Manoir, S , Joos, S., Werner, C. A., Fischer, K., Döhner, H., and Lichter, P. Comparative genomic hybridization in chronic B-cell leukemias shows a high incidence of chromosomal gains and losses Blood, 85: 3610-3618, 1995.
20. Joos, S., Bergerheim, U. S R., Pan, Y., Matsuyama, H , Bentz, M , du Manoir, S., and Lichter, P. Mapping of chromosomal gains and losses in prostate cancer by comparative genomic hybridization. Genes Chromosomes & Cancer, 14: 267-276, 1995
21. Voorter, C, Joos, S., Bringuier, P-P, Vallinga, M. Poddighe, P. Schalken, J., du Manoir, S., Ramaekers, F, Lichter, P., and Hopman, A. Detection of chromosomal imbalances in transitional cell carcinoma of the bladder by comparative genomic hybridization. Am J Pathol. 146 1341-1354, 1995.
22. Kallioniemi, O-P., Kallioniemi, A., Piper, J., Isola, J., Waldman, F. M., Gray, J. W., and Pminel, D. Optimizing comparative genomic hybridization for analysis of DNA sequence copy number changes in solid tumors. Genes Chromosomes & Cancer, 10: 231-243, 1994.
23. Genome Data Base, GDB (TM) The Human Genome Data Base Project Baltimore: The Johns Hopkins University, 1990-. Updated daily Available from Internet: URL.http://gdbuwvv.gdb.org/gdb/browser/docs/topq.html.
24. Caldas, C , Hahn, S. A , da Costa, L. T., Redston, M S., Schulte, M., Seymour, A. B , Weinstein, C L , Hruban, R H., Yeo, C. J , and Kern, S. E. Frequent somatic mutations and homozygous deletions of the p16 (MTS1) gene in pancreatic adenocarcinoma. Nat Genet., 8: 27-32, 1994.
25. Liu, Q., Yan, Y-X., McClure, M., Nakagawa, H., Fujimura, F , and Rustgi, A. K. MTS-1 (CDKN2) tumor suppressor gene deletions are a frequent event in esophagus squamous cancer and pancreatic adenocarcinoma cell lines. Oncogene, 10: 619-622, 1995
26. Bartsch, D., Shevlin, D. W , Tung, W S , Kisker, O , Wells, S. A., and Goodfellow, P. Frequent mutations of CDKN2 in primary pancreatic adenocarcinomas. Genes Chromosomes & Cancer, 14: 189-195, 1995.
27. Di Renzo, M F, Poulsom, R., Olivero, M., Comoglio, P M , and Lemoine, N. R. Expression of the Met/hepatocyte growth factor receptor in human pancreatic cancer Cancer Res., 55: 1129-1138, 1995.
28. Almoguera, C., Shibata, D , Forrester, K . Martin, J , Arnheim, N., and Perucho, M. Most human carcinomas of the exocrine pancreas contain mutant c-K-ras genes. Cell, 53: 549-554, 1988
29. Smit, V T. H B. M., Boot, A J. M , Smits, A M. M., Flueren, G. J , Cornelisse, C J., and Bos, J L KRAS codon 12 mutations occur very frequently in pancreatic adenocarcinomas. Nucleic Acids Res., 16, 7773-7782, 1988.