FHIT mutations in human primary gastric cancer

Cancer Research

Volumn 57, Issue 8, 1997, Pages 1435-1437

  Gemma, Akihiko ^a   Hagiwara, Koichi ^a   Ke, Yang ^b   Burke, Louise M ^a   Khan, Mohammed A ^a   Nagashima, Makoto ^a   Bennett, William P ^a   Harris, Curtis C ^a  

^a NATIONAL CANCER INSTITUTE   (United States)

^b PEKING UNIVERSITY HEALTH SCIENCE CENTER   (China)

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; ARTICLE; CHROMOSOME 3P; CLINICAL ARTICLE; GENE DELETION; GENE LOCATION; HUMAN; HUMAN TISSUE; MISSENSE MUTATION; PRIORITY JOURNAL; SINGLE STRAND CONFORMATION POLYMORPHISM; STOMACH CARCINOGENESIS; STOMACH CARCINOMA;

EID: 0030975628     PISSN: 00085472     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (24)

1. Whang-Peng, J., KaoShan, C. S., Lee, E. C., Bunn, P. A., Carney, D. N., Gazdar, A. F., and Minna, J. D. Specific chromosome defect associated with human small-cell lung cancer. Science (Washington DC), 275: 181-182, 1982.
2. Kok, H., Qsinga, J., Carrit, B., Davis, M. B., van der Veen, A. Y., Landsvater. R. M., de Leji L. F. M. H., Berendsen, H. H., Postmus, P. E., Poppema, S., and Buys, C. H. C. M. Deletion of a DNA sequence at the chromosomal region 3p21 in all major types of lung cancer. Nature (Lond.), 330: 578-581, 1987.
3. Naylor, S. L., Johnson, B. E., Minna, J. D., and Sakaguchi, A. Y. Loss of heterozygosity of chromosome 3p markers in small-cell lung cancer. Nature (Lond.), 329: 451-454, 1987.
4. Brauch, H., Johnson, B., Hovis, J., Yano, T., Gazdar, A., Pettengill, O. S., Graziano, S., Sorenson, G. D., Poiesz, B. J., Minna, J., Linehan, M., and Zbar, B. Molecular analysis of the short arm of chromosome 3 in small-cell and non-small-cell carcinoma of the lung. N. Engl. J. Med., 317: 1109-1113, 1987.
5. Yokota, J., Wada, M., Shimosato, Y., Terada, M., and Sugimura, T. Loss of heterozygosity on chromosomes 3, 13, 17 in small cell carcinoma and chromosome 3 in adenocarcinoma of the lung. Proc. Nail. Acad. Sci. USA, 84: 9252-9256, 1987.
6. Zbar, B., Brauch, H., Talmadge, C., and Linehan, M. Loss of alleles of loci on the short arm of chromosome 3 in renal cell carcinoma. Nature (Lond.), 327: 721-724, 1987.
7. Zeiger, M. A., Gnarra, J. R., Zbar, B., Linehan, W. M., and Pass, H. I. Loss of heterozygosity on the short arm of chromosome 3 in mesothelioma cell lines and solid tumors. Genes Chromosomes & Cancer, 11: 15-20, 1994.
8. Killary, A. M., Wolf, M. E., Giambernardi, T. A., and Naylor, S. L. Definition of a tumor suppressor locus within human chromosome 3p21-p22. Proc. Natl. Acad. Sci. USA, 89: 10877-10881, 1992.
9. Daly, M. C., Xiong, R. H., Buchhagen, D., Hensel, C. H., Garci, D. K., Killary, A. M., Minna, J. D., and Naylor, S. L. A homozygous deletion on chromosome 3 in a small cell lung cancer cell line correlates with a region of tumor suppressor activity. Oncogene, 8: 1721-1729, 1993.
10. Kok, K., Hosfra, R., Pilz, A., van den Berg, A., Terpstra, P., Buys, C. H., and Carrit, B. A gene in the chromosomal region 3p21 with greatly reduced expression in lung cancer is similar to the gene for ubiquitin activating enzyme. Proc. Natl. Acad. Sci. USA, 90: 6071-6075, 1993.
11. Linehan, W. M., Lerman, M. I., and Zbar, B. Identification of the von Hippel-Lindau (VHL) gene: its role in renal cancer. JAMA, 273: 564-570, 1995.
12. Gnarra, J. R., Tory, K., Weng, Y., Schmidt, L., et al. Mutations of the VHL tumor suppressor gene in renal carcinoma. Nat. Genet., 7: 85-90, 1994.
13. Kanno, H., Kondo, K., Ito, S., Yamamoto, S., Fuji, S., Torigoe, S., Sakai, N., Hosaka, M., Shuin, T., and Yao, M. Somatic mutations of the von Hippel-Lindau tumor suppressor gene in sporadic central nervous system hemangioblastomas. Cancer Res., 54:4845-4847, 1994.
14. Cohen, A. J., Li, F. P., Berg, S., Marchetto, D. J., Tsai, S., Jacobs, S. C., and Brown, R. S. Hereditary renal-cell carcinoma associated with a chromosomal translocation. N. Engl. J. Med., 301: 592-595, 1979.
15. Wang, N., and Perkins, K. L. Involvement of band 3pl4 in t(3:8) hereditary renal carcinoma. Cancer Genet. Cytogenet., 11: 479-481. 1984.
16. Paradee, W. W., Mullins, C., He, Z., Glover, T., Wilke, C., Opalka, B., Schutte, J., and Smith, D. I. Precise localization of aphidicolin-induced breakpoints on the short arm of human chromosome 3. Genomics, 27: 358-361, 1995.
17. Ohta, M., Inoue, H., Cotticelli, M. G., Kastury, K., Baffa, R., Palazo, J., Siprashvili, Z., Mori, M., McCue, P., Druck, T., Croce, C. M., and Huebner, K. The FHIT gene, spanning the chromosome 3p14.2 fragile site and renal carcinoma-associated t(3;8) breakpoint, is abnormal in digestive tract cancers. Cell, 84: 587-597, 1996.
18. Sozzi, G., Veronese, M. L., Negrini, M., Baffa, R., Cotticelli, M. G., Inoue, H., Tornielli, S., Pilolti, S., Gregorio, L. D., Pastorino, U., Pierotti, M. A., Ohta, M., Huebner, K., and Croce, C. M. The FHIT gene at 3p14.2 is abnormal in lung cancer. Cell, 85: 17-26, 1996.
19. Negrini, M., Monaco, C., Vorechovsky, I., Ohta, M., Druck, T., Baffa, R., Huebner, K., and Croce, C. M. The FHIT gene at 3p14.2 is abnormal in breast carcinomas. Cancer Res., 56: 3173-3179, 1996.
20. Sozzi, G., Alder, H., Tornielli, S., Corletto, V., Baffa, R., Veronese, M. L., Negrini, M., Pilotti, S., Pierotti, M. A., Huebner, K., and Croce, C. M. Aberrant FHIT transcripts in Merkel cell carcinoma. Cancer Res., 56: 2472-2474, 1996.
21. Thiagalingam, S., Lisitsyn, N. A. Hamaguchi, M., Wigler, M. H., Wilison, J. K. V., Markowitz, S. D., Leach, F. S., Kinzler, K. W., and Vogeistein, B. Evaluation of the FHIT gene in colorectal cancers. Cancer Res., 56: 2936-2939, 1996.
22. Takenoshita, S., Hagiwara, K., Nagashima, M., Gemma, A., Bennett, W. P., and Harris, C. C. The genomic structure of the gene encoding the human transforming growth factor β type II receptor (TGF-β RII). Genomics, 36: 341-344, 1996.
23. Hagiwara, K., and Harris, C. C. "Long distance sequencer method"; a novel strategy for large DNA sequencing projects. Nucleic Acids Res., 24: 2460-2461, 1996.
24. Gemma, A., Takenoshita, S., Hagiwara, K., Okamota, A., Spillare, E. A., McMenamin, M. G., Hussain, S. P., Forrester, K., Zariwala, M., Xiong, Y., and Harris, C. C. Molecular analysis of the cyclin dependent kinase inhibitor genes p15INK4b/MTS2, p16INK4/MTS1, p18 and p19 in human cancer cell lines. Int. J. Cancer, 68: 605-611, 1996.