No evidence of mutation in the human PTC gene, responsible for nevoid basal cell carcinoma syndrome, in human primary squamous cell carcinomas of the esophagus and lung

Japanese Journal of Cancer Research

Volumn 88, Issue 3, 1997, Pages 225-228

  Suzuki, Kazufumi ^a,b   Daigo, Yataro ^a   Fukuda, Seisuke ^a   Tokino, Takashi ^a   Isomura, Minoru ^a   Isono, Kaichi ^b   Wainwright, Brandon ^c   Nakamura, Yusuke ^a  

^a UNIVERSITY OF TOKYO   (Japan)

^b CHIBA UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^c UNIVERSITY OF QUEENSLAND   (Australia)

Author keywords

Chromosome 9q; PTC gene; Squamous cell carcinoma

Indexed keywords

DNA;

ARTICLE; BASAL CELL NEVUS SYNDROME; CANCER GENETICS; CARCINOGENESIS; CHROMOSOME 9Q; CLINICAL ARTICLE; DNA POLYMORPHISM; DNA SEQUENCE; ESOPHAGUS CARCINOMA; EXON; GENE MUTATION; GENE SEQUENCE; HEAD AND NECK CARCINOMA; HETEROZYGOSITY LOSS; HUMAN; HUMAN TISSUE; LUNG CARCINOMA; PRIORITY JOURNAL; SINGLE STRAND CONFORMATION POLYMORPHISM; SQUAMOUS CELL CARCINOMA; TUMOR SUPPRESSOR GENE; UTERUS CARCINOMA;

EID: 0030966117     PISSN: 09105050     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1349-7006.1997.tb00370.x     Document Type: Article

References (23)

1. Wicking, C., Berkman, J., Wainwright, B. and Chenevix-Trench, G. Fine genetic mapping of the gene for nevoid basal cell carcinoma. Genomics, 22, 505-511 (1994).
2. Goldstein, A. M., Stewart, C., Bale, S. J. and Dean, M. Localization of the gene for the nevoid basal cell carcinoma syndrome. Am. J. Hum. Genet., 54, 765-773 (1994).
3. Hahn, H., Christiansen, J., Wicking, C., Zaphiropoulos, P. G., Chidambaram, A., Gerrard, B., Vorechovsky, I., Bale, A. E., Toftgard, R., Dean, M. and Wainwright, B. A mammalian patched homolog is expressed in target tissues of sonic hedgehog and maps to a region associated with developmental abnormalities. J. Biol. Chem., 271, 12125-12128 (1996).
4. Hahn, H., Wicking, C., Zaphiropoulos, P. G., Gailani, M. R., Shanley, S., Chidambaram, A., Vorechovsky, I., Holmberg, E., Unden, A. B., Gillies, S., Negus, K., Smyth, I., Pressman, C., Leffell, D. J., Gerrard, B., Goldstein, A. M., Dean, M., Toftgard, R., Chenevix-Trench, G., Wainwright, B. and Bale, A. E. Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndrome. Cell, 85, 841-851 (1996).
5. Johnson, R.L., Rothman, A. L., Xie, J., Goodrich, L.V., Bare, J. W., Bonifas, J. M., Quinn, A. G., Myers, R. M., Cox, D. R., Epstein, E. H., Jr. and Scott, M. P. Human homolog of patched, a candidate gene for basal cell nevus syndrome. Science, 272, 1668-1671 (1996).
6. Aoki, T., Mori, T., Du, X., Nishihira, T., Matsubara, T. and Nakamura, Y. Allelotype study of esophageal carcinoma. Genes Chromosomes Cancer, 10, 177-182 (1994).
7. Mori, T., Yanagisawa, A., Kato, Y., Miura, K., Nishihira, T., Mori, S. and Nakamura, Y. Accumulation of genetic alterations during esophageal carcinogenesis. Hum. Mol. Genet., 3, 1969-1971 (1994).
8. Ah-See, K. W., Cooke, T. G., Pickfold, I. R., Soutar, D. and Balmain, A. An allelotype of squamous carcinoma of the head and neck using microsatellite markers. Cancer Res., 54, 1617-1621 (1994).
9. Sato, S., Nakamura, Y. and Tsuchiya, E. Difference of allelotype between squamous cell carcinoma and adenocarcinoma of the lung. Cancer Res., 54, 5652-5655 (1994).
10. Sato, T., Tanigami, A., Yamakawa, A., Akiyama, F., Kasumi, F., Sakamoto, G. and Nakamura, Y. Allelotype of breast cancer: cumulative allelic losses promote tumor progression in primary breast cancer. Cancer Res., 50, 7184-7189 (1990).
11. Lu, S.-H., Hsieh, L.-L., Lou, F. C. and Weinstein, I. B. Amplification of the EGF receptor and c-myc genes in human esophageal cancers. Int. J. Cancer, 42, 502-505 (1988).
12. Tsuda, T., Tahara, E., Kajiyama, G., Sakamoto, H., Terada, M. and Sugimura, T. High incidence of coamplification of hst-1 and int-2 genes in human esophageal carcinomas. Cancer Res., 49, 5505-5508 (1989).
13. Kitagawa, Y., Ueda, M., Ando, N., Shinozawa, Y., Shimizu, N. and Abe, O. Significance of int-2/hst-1 coamplification as a prognostic factor in patients with esophageal squamous carcinoma. Cancer Res., 51, 1504-1508 (1991).
14. Wagata, T., Ishizaki, K., Imamura, M., Shimada, Y., Ikenaga, M. and Tobe, T. Deletion of 17p and amplification of the int-2 gene in esophageal carcinomas. Cancer Res., 51, 2113-2117 (1991).
15. Jiang, W., Zhang, Y.-J., Kahn, S. M., Hollstein, M. C., Santella, R.M., Lu, S.-H., Harris, C. C., Montesano, R. and Weinstein, I. B. Altered expression of the cyclin D1 and retinoblastoma genes in human esophageal cancer. Proc. Natl. Acad. Sci. USA, 90, 9026-9030 (1993).
16. Huang, Y., Meltzer, S. J., Yin, J., Tong, Y., Chang, E. H., Srivastava, S., McDaniel, T., Boynton, R. F. and Zou, Z.-Q. Altered messenger RNA unique mutational profiles of p53 and Rb in human esophageal carcinomas. Cancer Res., 53, 1889-1894 (1993).
17. Wagata, T., Shibagaki, I., Imamura, M., Shimada, Y., Toguchida, J., Yandell, D. W., Ikegawa, M., Tobe, T. and Ishizaki, K. Loss of 17p mutation of p53 gene and overexpression of p53 protein in esophageal squamous cell carcinomas. Cancer Res., 53, 846-850 (1993).
18. Meltzer, S. J., Yin, J., Huang, Y., McDaniel, T. K., Newkirk, C., Iseri, O., Vogelstein, B. and Resau, J. H. Reduction to homozygosity involving p53 in esophageal cancers demonstrated by the polymerase chain reaction. Proc. Natl. Acad. Sci. USA, 88, 4976-4980 (1991).
19. Hollstein, M. C., Metcalf, R. A., Welsh, J. A., Montesano, R. and Harris, C. C. Frequent mutation of the p53 gene in human esophageal cancer. Proc. Natl. Acad. Sci. USA, 87, 9958-9961 (1990).
20. Knowles, M. A., Elder, P. A., Williamson, M., Cairns, J. P., Shaw, M. E. and Law, M. G. Allelotype of human bladder cancer. Cancer Res., 54, 531-538 (1994).
21. Orlow, I., Lianes, P., Lacombe, L., Dalbagni, G., Reuter, V. E. and Cardo, C. C. Chromosome 9 allelic losses and microsatellite alterations in human bladder tumors. Cancer Res., 54, 2848-2851 (1994).
22. Miura, K., Suzuki, K., Tokino, T., Isomura, M., Inazawa, J., Matsuno, S. and Nakamura, Y. Detailed deletion mapping in squamous cell carcinomas of the esophagus narrows a region containing a putative tumor suppressor gene to about 200 kilobases on distal chromosome 9q. Cancer Res., 56, 1629-1634 (1996).
23. Goudie, D. R., Yuille, M. A. R., Leversha, M. A., Furlong, R. A., Carter, N. P., Lush, M. J., Affara, N. A. and Ferguson-Smith, M. A. Multiple self-healing squamous epitheliomata (ESS1) mapped to chromosome 9q22-q31 in families with common ancestry. Nat. Genet., 3, 165-169 (1993).