Effects of cyclin D1 polymorphism on age of onset of hereditary nonpolyposis colorectal cancer

Cancer Research

Volumn 60, Issue 2, 2000, Pages 249-252

  Kong, Shouming ^a   Amos, Christopher I ^a   Luthra, Rajyalakshmi ^a   Lynch, Patrick M ^a   Levin, Bernard ^a   Frazier, Marsha L ^a  

^a UNIVERSITY OF TEXAS MD ANDERSON CANCER CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CYCLIN D1;

ADULT; ARTICLE; COLORECTAL CANCER; DNA POLYMORPHISM; DNA SEQUENCE; FEMALE; GENE MUTATION; HUMAN; MALE; ONSET AGE; PHENOTYPE; PRIORITY JOURNAL; RNA SPLICING;

ADULT; AGE OF ONSET; AGED; AGED, 80 AND OVER; BASE PAIR MISMATCH; BASE SEQUENCE; CARRIER PROTEINS; CELL CYCLE; COLORECTAL NEOPLASMS, HEREDITARY NONPOLYPOSIS; CYCLIN D1; DNA-BINDING PROTEINS; ETHNIC GROUPS; FEMALE; FUNGAL PROTEINS; HETEROZYGOTE DETECTION; HOMOZYGOTE; HUMANS; MALE; MIDDLE AGED; MUTATION, MISSENSE; MUTS HOMOLOG 2 PROTEIN; NEOPLASM PROTEINS; NUCLEAR PROTEINS; POLYMORPHISM, GENETIC; PROTO-ONCOGENE PROTEINS; SURVIVAL ANALYSIS;

EID: 0034650542     PISSN: 00085472     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (16)

1. Fishel, R., Lescoe, M. K., Rao, M. R. S., Copeland, N. G., Jenkins, N. A., Garber, J., Kane, M., and Kolodner, R. D. The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer. Cell, 75: 1027-1038, 1993.
2. Aaltonen, L. A., Peltomaki, P., Leach, F. S., Sistonen, P., Pylkkanen, L., Mecklin, J. P., Jarvinen, H., Powell, S. M., Jen, J., Hamilton, S. R., Kinzler, K. W., Vogelstein, B., and de la Chapelle, A. Clues to the pathogenesis of familial colorectal cancer. Science (Washington DC), 260: 812-816, 1993.
3. Leach, F. S., Nicolaides, N. C., Papadopoulos, N., Liu, B., Jen, J., Parsons, R., Peltomaki, P., Sistonan, P., Aaltonen, L. A., Nystrom, L., Guan, Y. Y., Zhang, J., Meltzer, P. S., Yu, J. W., Kao, F. T., Chen, D. J., Cerosaletti, K. M., Fournier, R. E. K., Todd, S., Lewis, T., Leach, R. J., Naylor, S. R., Green, J., Jass, J., Watson, P., Lynch, H. T., Trent, J. M., de la Chapelle, A., Kinzler, K. W., and Vogelstein, B. Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer. Cell, 75: 1215-1225, 1993.
4. Papadopoulos, N., Nicolaides, N. C., Wei, Y. F., Rube, S. M., Carter, K. C., Rosen, C. A., Haseltine, W. A., Fleischman, R. D., Fraser, C. M., Adams, M. D., Venter, J. C., Hamilton, S. R., Peterson, G. M., Watson, P., Lynch, H. T., Peltomaki, P., Mecklin, J. P., de la Chapelle, A., Kinzler, K. W., and Vogelstein, B. Mutation of a mutL homolog in hereditary colon cancer. Science (Washington DC), 263: 1625-1629, 1994.
5. Bronner, C. E., Baker, S. M., Morrison, P. T., Warren, G., Smith, L. G., Lescoe, M. K., Kane, M., Earabino, C., Lipford, J., Lindblom, A., Tannergard, P., Bollag, R. J., Godwin, A. R., Ward, D. C., Nordenskjold, M., Fishel, R., Kolodner, R., and Liskay, R. M. Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary nonpolyposis colon cancer. Nature (Lond.), 368: 258-261, 1994.
6. Miyaki, M., Konishi, M., Tanaka, K., Kikuchi-Yanoshita, R., Muraoka, M., Yasuno, M., Igari, T., Koike, M., Chiba, M., and Mori, T. Germline mutation of MSH6 as the cause of hereditary nonpolyposis colorectal cancer. Nat. Genet., 17: 271-272, 1997.
7. Liu, B., Nicolaide, N. C., Markowitz, S., Willson, J. K. V., Parson, R. E., Jen, J., Papadopolous, N., Peltomaki, P., de la Chapelle, A., Hamilton, S. R., Kinzler, K. W., and Vogelstein, B. Mismatch repair gene defects in sporadic colorectal cancers with microsatellite instability. Nat. Genet., 9: 48-55, 1995.
8. Jeon, H. M., Lynch, P. M., Howard, L., Ajani, J., Levin, B., and Frazier, M. L. Mutation of the hMSH2 gene in two families with hereditary nonpolyposis colorectal cancer. Hum. Mutat., 7: 327-333, 1996.
9. Lynch, H. T., Watson, P., Lanspa, S. J. Marcus, J., Smyrk, T., Fitzgibbons, R. J., Kriegler, M., and Lynch, J. F. Natural history of colorectal cancer in hereditary nonpolyposis colorectal cancer (Lynch syndrome I and II). Dis. Colon Rectum, 31: 439-444, 1988.
10. Donnellan, R., and Chetty, R. Cyclin D1 and human neoplasia. Mol. Pathol., 51: 1-7, 1998.
11. Betticher, D. C., Thatcher, N., Altermatt, H. J., Hoban, P., Ryder, D. J., and Heighway, J. Alternate splicing produces a novel cyclin D1 transcript. Oncogene, 11: 1005-1011, 1995.
12. Xiong, Y., Menninger, J., Beach, D., and Ward, D. C. Molecular cloning and chromosomal mapping of CCND genes encoding human D-type cyclins. Genomics, 13: 575-584, 1992.
13. Matthias, C., Branigan, K., Jahnke, V., Leter, K., Haas, J., Heighway, J., Jones, P. W., Strange, R. C., Fryer, A. A., and Hoban, P. R. Polymorphism within the cyclin D1 gene is associated with prognosis in patients with squamous cell carcinoma of the head and neck. Clin. Cancer Res., 4: 2411-2418, 1998.
14. Lee E. T. Statistical methods for survival analysis. New York: John Wiley and Sons, 1992.
15. Kinzler, K. W., and Vogelstein, B. Mismatch repair gene defects in sporadic colorectal cancers with microsatellite instability. Nat. Genet., 9: 48-55, 1995.
16. Rogers, S., Wells, R., and Rechsteiner, M. Amino acid sequences common to rapidly degraded proteins: the PEST hypothesis. Science (Washington DC), 234: 364-368, 1986.