Loss of heterozygosity in laryngeal squamous cell carcinoma;ALLELVERLUSTE BEI PLATTENEPITHEL-KARZINOMEN DES LARYNX

Laryngo- Rhino- Otologie

Volumn 75, Issue 1, 1996, Pages 48-52

  Bockmühl, Ulrike ^a   Petersen, I ^a   Dietel, M ^a  

^a HUMBOLDT UNIVERSITY   (Germany)

Author keywords

Chromosomal arms 3p, 5q, 9p, 9q, 17p; Laryngeal squamous cell carcinoma; Loss of heterozygosity; Tumor suppressor genes

Indexed keywords

DNA;

ADULT; AGED; ALLELE; ARTICLE; CLINICAL ARTICLE; FEMALE; GEL ELECTROPHORESIS; HETEROZYGOSITY; HUMAN; LARYNX CARCINOMA; MALE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PROGNOSIS;

EID: 0030020128     PISSN: 09358943     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2007-997531     Document Type: Article

References (37)

1. Adamson, R., A. S. Jones, J. K. Field: Loss of heterozygosity studies on chromosome 17 in head and neck cancer using microsatellite markers. Oncogene 9 (1994) 2077-2082
2. Ah-See, K. W., T. G. Cooke, I. R. Pickford, D. Soutar, A. Balmain: An allelotype of squamous carcinoma of the head and neck using microsatellite markers. Cancer Res. 54 (1994) 1617-1621
3. Clasen, B. P. E., S. Kellermann, H. J. Steinhoff, W. Schwab: Das Larynxkarzinom in Deutschland. Otorhinolaryngol. Nova 1 (1991) 321-327
4. Cunningham, C.,. M. G. Dunlop, A. H. Wyllie, C. C. Bird: Deletion mapping in colorectal cancer of a putative tumor suppressor gene in 8 p22-p21.3. Oncogene 8 (1993) 1391-1396
5. Dixon, J., M. J. Dixon: Trinucleotide repeat polymorphism at the D5 S373 locus. Hum. Mol. Genet. 2 (1993) 829
6. El-Naggar, A. K. M.-S. Lee, G. Wang, M. A. Luna, H. Goepfert, J. G. Batsakis: Polymerase chain reaction-based restriction fragment length polymorphism analysis of the short arm of chromosome 3 in primary head and neck squamous cell carcinoma. Cancer 72 (1993) 881-886
7. Furlong, R. A., J. E. W. Lyall, M. J. Lush, N. A. Affara, M. A. Ferguson-Smith: Four dinucleotide repeat polymorphisms on chromosome 9 (D9 S143-146). Hum. Mol. Genet. 1 (1992) 447
8. Hauser-Urfer, I. F, J. Stauffer: Comparative chromosome analysis of nine squamous cell carcinoma real lines from tumors of the head and neck. Cytogenet. Cell Genet. 39 (1985) 35-39
9. Hibi, K., T. Takahashi, K. Yamakawa, R. Ueda, Y. Sekido, Y. Aryoshi: Three distinct regions involved in 3 p deletion in human lung cancer. Oncogene 7 (1992) 445-449
10. Jahnke, V.: Bösartige Tumoren des Larynx. In Naumann, H. H., J. Helms, C. Herberhold, E. Kastenbauer (Hrsg.): Oto-Rhino-Laryngologie in Klinik und Praxis. Bd. 3. Thieme, Stuttgart 1995 (388-421)
11. Jones, M. H., K. Yamakawa, Y. Nakamura: Isolation and characterization of 19 dinucleotide repeat polymorphisms on chromosome 3 p. Hum. Mol. Genet. 1 (1992) 131-133
12. Jones, M. H., Y. Nakamura: Detection of loss of heterozygosity at the human TP53 locus using a dinucleotide repeat polymorphism. Genes Chrom. Cancer 5 (1992) 89-90
13. Koorey, D. J., G. W. McCaughan, R. J. Trent, N. D. Gallagher: Dinucleotide repeat polymorphism at the D5 S134 locus linked to the adenomatous polyposis coli (APC) gene. Hum. Mol. Genet. 1 (1992) 655
14. Latif, F., M. Fivash, G. Glenn, K. Tory, M. L. Orcutt, K. Hampsch, J. Delisio, M. Lerman, J. Cowan, M. Beckett, R. R. Weichselbaum: Chromosome 3 p deletions in head and neck carcinoma: Statistical ascertainment of allelic loss. Cancer Res. 52 (1992) 1451-1456
15. Li, X., N. K. Lee, Y.-W. Ye, P. G. Waber, C. Schweitzer, Q.-C. Cheng, P. D. Nisen: Allelic loss at chromosomes 3p, 8p, 13 p, and 17 p associated with poor prognosis in head and neck cancer. J. Natl. Cancer Inst. 86 (1994) 1524-1529
16. Maestro, R., D. Gasparotto, T. Vukosavljevic, L. Barzan, S. Sulfaro, M. Boiocchi: Three discrete regions of deletion at 3 p in head and neck cancers. Cancer Res. 53 (1993) 5775-5779
17. Merlo, A., E. Gabrielson, F. Askin, D. Sidransky: Frequent loss of chromosome 9 in human primary non-small cell lung cancer. Cancer Res. 54 (1994) 640-642
18. Nawroz, H., P. van der Riet, R. H. Hruban, W. Koch, J. M. Ruppert, D. Sidransky: Allelotype of head and neck squamous cell carcinoma. Cancer Res. 54 (1994) 1152-1155
19. Oliphant, A. R., E. C. Wright, J. Swensen, N. A. Gruis, D. Goldgar, M. H. Skolnick: Dinucleotide repeat polymorphism at the D17S513 locus. Nucleic Acids Res. 19 (1991) 4794
20. Olumi, A. F., E. C. Skinner, Y. C. Tsai, P. A. Jones: Molecular analysis of human bladder cancer. Semin. Urol. 8 (1990) 270-277
21. Osborne, R. J., V. Leech: Polymerase chain reaction allelotyping of human ovarian cancer. Br. J. Cancer 69 (1994) 429-438
22. Partridge, M., S. Kiguwa, J. D. Langdon: Frequent deletion of chromosome 3 p in oral squamous cell carcinoma. Oral Oncol. Eur. J. Cancer 30b (1994) 248-251
23. Petersen, I., G. Heinemann, T. Ried, M. Dietel: Nicht-radioaktive Detektion von Mikrosatelliten-Polymorphismen zur Bestimmung eines Allelverlustes (LOH): DNA-Verlust auf Chromosom 3 p und 5 q in kleinzelligen Lungenkarzinomen delektiert mittels LOH und CGH. Verh. Dtsch. Ges. Path. 78 (1994) 237
24. Rudert, H.: Maligne Tumoren der Lippen, der Mundhöhle und des Oropharynx. In Naumann, H. H., J. Helms, C. Herberhold, E. Kastenbauer (Hrsg.): Oto-Rhino-Laryngologie in Klinik und Praxis. Bd. 2. Thieme, Stuttgart 1995 (648-675)
25. Sambrook, J., E. F. Fritsch, T. Maniatis: Molecular Cioning. A laboratory manual. Cold Spring Harbor Laboratory Press (1989)
26. Sarot, Avyama, F., G. Sakamoto, F. Kasumi, Y. Nakamura: Accumulation of genetic alterations and progression of primary breast cancer. Cancer Res. 51 (1991) 5794-5799
27. Scholnick, S. B., P. C. Sun, M. E. Shaw, B. H. Haughey, S. K. ElMofty: Frequent loss of heterozygosity for Rb, TP53, and chromosome arm 3 p, but not NME1 in squamous cell carcinomas of the supraglottic larynx. Cancer 73 (1994) 2472-2480
28. Shibagaki, I., Y. Snimada, T. Wagata, M. Ikenaga, M. Imamura, K. Ishizaki: Allelotype analysis of esophageal squamous cell carcinoma. Cancer Res. 54 (1994) 2996-3000
29. Somers, K. D., M. A. Merrick, M. E. Lopez, L. S. Incognito, G. L. Schlechter, G. Casey: Frequent p53 mutations in head and neck cancer. Cancer Res. 52 (1992) 5997-6000
30. Tsuchiya, E., Y. Nakamura, S.-Y. Weng, K. Nakagawa, S. Tsuchiya, H. Sugano, T. Kitagawa: Allelotype of non-small cell lung carcinoma - comparison between loss of heterozygosity in squamous cell carcinoma and adenocarcinoma. Cancer Res. 52 (1992) 2478-2481
31. van der Riet, P., H. Nawroz, R. H. Hruban, R. Corio, K. Tokino, W. Koch, D. Sidransky: Frequent loss of chromosome 9 p21-22 early in head and neck cancer progression. Cancer Res. 54 (1994) 1156-1158
32. Vogelstein, B., E. R. Fearon, S. R. Hamilton: Genetic alterations during colorectal tumor development. N. Engl. J. Med. 319 (1992) 525-532
33. Weinberg, R. A.: Tumor suppressor genes. Science 254 (1991) 1138
34. Yamakawa, K., T. Takahashi, Y. Horio: Frequent homozygous deletions in lung cancer cell lines detected by DNA marker located at 3 p21.3-p22. Oncogene 8 (1993) 327-330
35. Yokota, J., Y. Tsukada, T. Nakajima, M. Gotoh, Y. Shimosato, N. Mori, Y. Tsunokawa, T. Sugimura, M. Terada: Loss of heterozygosity on the short arm of chromosome 3 in carcinoma of the uterine cervix. Cancer Res. 49 (1989) 3598-3601
36. Yoo, G. H., H.-J. Xu, J. A. Brennan, W. Westra, R. H. Hruban, W. Koch, W. F. Benedict, D. Sidransky: Infrequent inactivation of the retinoblastoma gene despite frequent loss of chromosome 13 q in head and neck squamous cell carcinoma. Cancer Res. 54 (1994) 4603-4606
37. Zbar, B.: Chromosomal deletions in lung cancer and renal cancer. In DeVita, V. T., S. Hellman, S. A. Rosenberg (Hrsg.): Important advances in oncology 1989. J. B. Lippincott Co., Philadelphia 1989 (41-60)