Patterns of chromosomal alterations in metastasizing and nonmetastasizing primary head and neck carcinomas

Cancer Research

Volumn 57, Issue 23, 1997, Pages 5213-5216

  Bockmühl, Ulrike ^a   Petersen, Simone ^a   Schmidt, Sven ^a   Wolf, Günter ^a   Jahnke, Volker ^a   Dietel, Manfred ^a   Petersen, Iver ^a  

^a CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

MICROSATELLITE DNA;

ARTICLE; CHROMOSOME 10Q; CONTROLLED STUDY; DISEASE ASSOCIATION; GENE DELETION; GENETIC HETEROGENEITY; GENETIC POLYMORPHISM; HEAD AND NECK CANCER; HETEROZYGOSITY; HISTOGRAM; HUMAN; HUMAN CELL; HUMAN TISSUE; METASTASIS; PHENOTYPE; PRIORITY JOURNAL; RESPIRATORY TRACT CANCER; SQUAMOUS CELL CARCINOMA; STATISTICAL ANALYSIS;

CARCINOMA, SQUAMOUS CELL; CHROMOSOME ABERRATIONS; CHROMOSOME DELETION; CHROMOSOME DISORDERS; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN; CHROMOSOMES, HUMAN, PAIR 10; COHORT STUDIES; FEMALE; GENETIC MARKERS; HEAD AND NECK NEOPLASMS; HUMANS; MALE; NEOPLASM METASTASIS; NEOPLASM STAGING;

EID: 0030715089     PISSN: 00085472     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (26)

1. Parker, S. L., Tong, T., Bolden, S., and Wingo, P. A. Cancer statistics, 1997. CA Cancer J. Clin., 47: 5-27, 1997.
2. Leemans, C. R., Tiwari, R., Nauta, J. J., van der Waal, I., and Snow, G. B. Recurrence at the primary site in head and neck cancer and the significance of lymph node metastases as a prognostic factor. Cancer (Phila.), 73: 187-190, 1994.
3. Brzoska, P. M., Levin, N. A., Fu, K. K., Kaplan, M. J., Singer, M. I., Gray, J. W., and Christman, M. F. Frequent novel DNA copy number increases in squamous cell head and neck tumors. Cancer Res., 55: 3055-3059, 1995.
4. Nawroz, H., van der Riet, P., Hruban, R. H., Koch, W., Ruppert, J. M., and Sidransky, D. Allelotype of head and neck squamous cell carcinoma. Cancer Res., 54: 1152-1155, 1994.
5. van Dyke, D. L., Worsham, M. J., Benninger, M. S., Krause, C. J., Baker, S. R., Wolf, G. T., Drumheller, T., Tilley, B. C., and Carey, T. E. Recurrent cytogenetic abnormalities in squamous cell carcinomas of the head and neck region. Genes Chromosomes Cancer, 9: 192-206, 1994.
6. Califano, J., van der Riet, P., Westra, W., Nawroz, H., Clayman, G., Piantadosi, S., Corio, R., Lee, D., Greenberg, B., Koch, W., and Sidransky, D. Genetic progression model for head and neck cancer: implications for field cancerization. Cancer Res., 56: 2488-2492, 1996.
7. Bockmühl, U., Schwendel, A., Dietel, M., and Petersen, I. Distinct patterns of chromosomal alterations in high and low grade head and neck squamous cell carcinomas. Cancer Res., 56: 5325-5329, 1996.
8. Petersen, I., Langreck, H., Wolf, G., Schwendel, A., Psille, R., Vogt, P., Reichel, M., Ried, T., and Dietel, M. Small cell lung cancer is characterized by a high incidence of deletions on chromosomes 3p, 4q, 5q, 10q, 13q and 17p. Br. J. Cancer, 75: 79-86, 1997.
9. Roth, K., Wolf, G., Dietel, M., and Petersen, I. Image analysis for comparative genomic hybridization (CGH) by a Windows-based karyotyping program. Anal. Quant. Cytol. Histol., in press, 1997.
10. Dib, C., Faure, S., Fizames, C., Samson, D., Drouot, N., Vignal, A., Millasseau, P., Marc, S., Kazan, J., Seboun, E., Lathrop, M., Gyapay, G., Morissette, J., and Weissenbach, J. A comprehensive genetic map of the human genome based on 5.264 microsatellites. Nature (Lond.), 380: 152-154, 1996.
11. Petersen, S., Wolf, G., Bockmühl, U., Gellert, K., Dietel, M., and Petersen, I. Deletions on chromosome 10q in human lung cancer: association with tumor progression and metastatic phenotype. Br. J. Cancer, 77: 270-276, 1998.
12. Petersen, I., Bujard, M., Petersen, S., Wolf, G., Goeze, A., Schwendel, A., Langreck, H., Gellert, K., Reichel, M., Just, K., du Manoir, S., Cremer, T., Dietel, M., and Ried, T. Patterns of chromosomal imbalances in adenocarcinoma and squamous cell carcinoma of the lung. Cancer Res., 57: 2331-2335, 1997.
13. Boukamp, P., Popp, S., Altmeyer, S., Hülsen, A., Fasching, C., Cremer, T., and Fusenig, N. E. Sustained nontumorigenic phenotype correlates with a largely stable chromosome content during long-term culture of the human keratinocyte line HaCaT. Genes Chromosomes Cancer, 19: 201-214, 1997.
14. Piper, J., Rutovitz, D., Sudar, D., Kallioniemi, A., Kallioniemi, O-P., Waldman, F. M., Gray, J. W., and Pinkel, D. Computer image analysis of comparative genomic hybridization. Cytometry, 19: 10-26, 1995.
15. Isola, J. I., Kallioniemi, O. P., Chu, L. W., Fuqua, S. A. W., Hilsenbeck, S. G., Osborne, C. K., and Waldman, F. M. Genetic aberrations detected by comparative genomic hybridization predict outcome in node-negative breast cancer. Am. J. Pathol., 147: 905-911, 1995.
16. Günthert, U., Hofmann, M., Rudy, W., Reber, S., Zoller, M., Haussmann, I., Matzku, S., Wenzel, A., Ponta, H., and Herrlich, P. A new variant of glycoprotein CD44 confers metastatic potential to rat carcinoma cells. Cell, 65: 13-24, 1991.
17. Gao, A. C., Lou, W., Dong, J. T., and Isaacs, J. T. CD44 is a metastasis suppressor gene for prostatic cancer located on human chromosome 11p13. Cancer Res., 57: 846-849, 1997.
18. Rempel, S. A., Schwechheimer, K., Davis, R. L., Cavenee, W. K., and Rosenblum, M. L. Loss of heterozygosity for loci on chromosome 10 is associated with morphologically malignant meningioma progression. Cancer Res., 53: 2386-2392, 1993.
19. Komiya, A., Suzuki, H., Ueda, T., Yatani, R., Emi, M., Ito, H., and Shimazaki, J. Allelic losses at loci on chromosome 10 are associated with metastasis and progression of human prostate cancer. Genes Chromosomes Cancer, 17: 245-253, 1996.
20. Eagle, L. R., Yin, X., Brothman, A. R., Williams, B. J., Atkin, N. B., and Prochownik, E. V. Mutation of the Mxil gene in prostate cancer. Nat. Genet., 9: 249-255, 1995.
21. Li, J., Yen, C., Liaw, D., Podsypania, K., Bose, S., Wang, S. I., Pue, J., Miliaresis, C., Rodgers, L., McCombie, R., Bigner, S. H., Giovanella, B. C., Ittmann, M., Tycko, B., Hibshoosh, H., Wigler, M. H., and Parsons, R. PTEN, a putative protein tyrosine phosphatase gene mutated in human brain, breast, and prostate cancer. Science (Washington DC), 275: 1943-1947, 1997.
22. Steck, P. A., Pershouse, M. A., Jasser, S. A., Yung, W. K. A., Lin, H., Ligon, A. H., Langford, L. A., Baumgard, M. L., Hattier, T., Davis, T., Frye, C., Hu, R., Swedlund, B., Teng, D. H. F., and Tavtigan, S. V. Identification of a candidate tumour suppressor gene, MMAC1, at chromosome 10q23.3 that is mutated in multiple advanced cancers. Nat. Genet., 15: 356-362, 1997.
23. Gray, I. C., Phillips, S. M. A., Lee, S. J., Neoptolemos, J. P., Weissenbach, J., and Spurr, N. K. Loss of the chromosomal region 10q23-25 in prostate cancer. Cancer Res., 55: 4800-4803, 1995.
24. Lin, J. C., Scherer, S. W., Tougas, L., Traverse, G., Tsui, L-C., Andrulis, I. L., Jothy, S., and Park, M. Detailed deletion mapping with a refined physical map of 7q31 localizes a putative tumor suppressor gene for breast cancer in the region of MET. Oncogene, 13: 2001-2008, 1996.
25. Rosen, E. M., Knesel, J., Goldberg, I. D., Jin, L., Bhargava, M., Joseph, A., Zitnik, R., Wines, J., Kelley, M., and Rockwell, S. Scatter factor modulates the metastatic phenotype of the EMT6 mouse mammary tumor. Int. J. Cancer, 57: 706-714, 1994.
26. Wick, W., Petersen, I., Schmutzler, R. K., Wolfarth, B., Lenartz, D., Bierhoff, E., Hümmerich, J., Müller, D. J., Stangl, A. P., Schramm, J., Wiestler, O. D., and von Deimling, A. Evidence for a novel tumor suppressor gene on chromosome 15 associated with progression to a metastatic stage in breast cancer. Oncogene, 12: 973-978, 1996.