Widespread skeletal metastatic potential of human lung cancer revealed by green fluorescent protein expression

Cancer Research

Volumn 58, Issue 19, 1998, Pages 4217-4221

  Yang, Meng ^a,b,c   Hasegawa, Satoshi ^a,b,c   Jiang, Ping ^a   Wang, Xiaoen ^a   Tan, Yuying ^a   Chishima, Takashi ^a,b,c   Shimada, Hiroshi ^b   Moossa, A R ^c   Hoffman, Robert M ^a,c  

^a ANTICANCER INC   (United States)

^b YOKOHAMA CITY UNIVERSITY   (Japan)

^c UNIVERSITY OF CALIFORNIA SAN DIEGO   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GREEN FLUORESCENT PROTEIN;

ANIMAL CELL; ARTICLE; BONE METASTASIS; EXPRESSION VECTOR; FLUORESCENCE; LUNG NON SMALL CELL CANCER; METASTASIS POTENTIAL; MOLECULAR CLONING; NONHUMAN; NUDE MOUSE; PRIORITY JOURNAL; PROTEIN EXPRESSION;

3T3 CELLS; ADRENAL GLAND NEOPLASMS; ANIMALS; BONE NEOPLASMS; BRAIN NEOPLASMS; FEMALE; GREEN FLUORESCENT PROTEINS; HUMANS; KIDNEY NEOPLASMS; LIVER NEOPLASMS; LUMINESCENT PROTEINS; LUNG NEOPLASMS; MICE; MICE, NUDE; NEOPLASM METASTASIS; RECOMBINANT PROTEINS; SPLENIC NEOPLASMS; TRANSFECTION; TRANSPLANTATION, HETEROLOGOUS; TUMOR CELLS, CULTURED;

EID: 0032188762     PISSN: 00085472     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (20)

1. Foundation for Promotion of Cancer Research. In: T. Kakizoe (ed.), Cancer Statistics in Japan, pp. 31-67. Tokyo: Foundation for Promotion of Cancer Research, 1997.
2. Hruban, R. H., van Mansfeld, A. D. M., Offerhaus, G. J., van Weering, D. H. J., Allison, D. C., Goodman, S. N., Kensler, T. W., Bose, K. K., Camcron, J. L., and Bos, J. L. K-ras oncogene activation in adenocarcinoma of the human pancreas. A study of 82 carcinomas using a combination of mutant-enriched polymerase chain reaction analysis and allele-specific oligonucleotide hybridization. Am. J. Pathol., 143: 545-554, 1993.
3. Redston, M. S., Caldas, C., Seymour, A. B., Hruban, R. H., da Costa, L. T., Yeo, C. J., and Kern, S. E. p53 mutations in pancreatic carcinoma and evidence of common involvement of homocopolymer tracts in DNA microdeletions. Cancer Res., 54: 3025-3033, 1994.
4. Caldas, C., Hahn, S. A., da Costa, L. T., Redston, M. S., Schutte, M., Seymour, A. B., Weinstein, C. L., Hruban, R. H., Yeo, C. J., and Kern, S. E. Frequent somatic mutations and homozygous deletions of the p16 (MTSI) gene in pancreatic adenocarcinoma. Nat. Genet., 8: 27-32, 1994.
5. Hahn, S. A., Schutte, M., Hoque, A. T. M. S., Moskaluk, C. A., da Costa, L. T., Rozenblum, E., Weinstein, C. L., Fischer, A., Yeo, C. J., Hruban, R. H., and Kern, S. E. DPC4, a candidate tumor suppressor gene at human chromosome 18q21.1. Science (Washington DC), 271: 350-353, 1996.
6. Griffin, C. A., Hruban, R. H., Morsberger, L. A., Ellingham, T., Long, P. P., Jaffee, E. M., Hauda, K. M., Bohlander, S. K., and Yeo, C. J. Consistent chromosome abnormalities in adenocarcinoma of the pancreas. Cancer Res., 55: 2394-2399, 1995.
7. Hahn, S. A., Seymour, A. B., Hoque, A. T. M. S., Schutte, M., da Costa, L. T., Redston, M. S., Caldas, C., Weinstein, C. L., Fischer, A., Yeo, C. J., Hruban, R. H., and Kern, S. E. Allelotype of pancreatic adenocarcinoma using xenograft enrichment. Cancer Res., 55: 4670-4675, 1995.
8. Kimura, M., Abe, T., Sunamura, M., Matsuno, S., and Horii, A. Detailed deletion mapping on chromosome arm 12q in human pancreatic adenocarcinoma: identification of a 1-cM region of common allelic loss. Genes Chromosomes Cancer, 17: 88-93, 1996.
9. Solinas-Toldo, S., Wallrapp, C., Müller-Pillasch, F., Bentz, M., Gress, T., and Lichter, P. Mapping of chromosomal imbalances in pancreatic carcinoma by comparative genomic hybridization. Cancer Res., 56: 3803-3807, 1996.
10. Fukushige, S., Waldman, F. M., Kimura, M., Abe, T., Furukawa, T., Sunamura, M., Kobari, M., and Horii, A. Frequent gain of copy number on the long arm of chromosome 20 in human pancreatic adenocarcinoma. Genes Chromosomes Cancer, 19: 161-169, 1997.
11. Mahlamäki, E. H., Höglund, M., Gorunova, L., Karhu, R., Dawiskiba, S., Andrén-Sandberg, Å., Kallioniemi, O-P., and Johansson, B. Comparative genomic hybridization reveals frequent gains of 20q, 8q, 11q, 12p, and 17q, and losses of 18q, 9p, and 15q in pancreatic cancer. Genes Chromosomes Cancer, 20: 383-391, 1997.
12. Caldas, C., Hahn, S. A., Hruban, R. H., Redston, M. S., Yeo, C. J., and Kern, S. E. Detection of K-ras mutations in the stool of patients with pancreatic adenocarcinoma and pancreatic ductal hyperplasia. Cancer Res., 54: 3568-3573, 1994.
13. Suzuki, H., Yoshida, S., Ichikawa, Y., Yokota, H., Mutoh, H., Koyama, A., Fukazawa, M., Todoroki, T., Fukao, K., Uchida, K., and Miwa, M. Ki-ras mutations in pancreatic secretions and aspirates from two patients without pancreatic cancer. J. Natl. Cancer Inst., 86: 1547-1549, 1994.
14. Goodale, R. L., Gajl-Peczalska, K., Dressel, T., and Samuelson, J. Cytologic studies for the diagnosis of pancreatic cancer. Cancer (Phila.), 47: 1652-1655, 1981.
15. Donlon, T. A., Brans, G. A., Latt, S. A., Mulholland, J., and Wyman, A. R. A chromosome 8-enriched alphoid repeat. Cytogenet. Cell Genet., 46: 607, 1987.
16. Moyzis, R. K., Albright, K. L., Bartholdi, M. F., Cram, L. S., Deaven, L. L., Hildebrand, C. E., Joste, N. E., Longmire, J. L., Meyne, J., and Schwarzacher-Robinson, T. Human chromosome-specific repetitive DNA sequences: novel markers for genetic analysis. Chromosoma, 95: 375-386, 1987.
17. Waye, J. S., and Willard, H. F. Structure, organization, and sequence of alpha satellite DNA from human chromosome 17: evidence for evolution by unequal crossing-over and an ancestral pentamer repeat shared with the human X chromosome. Mol. Cell. Biol., 6: 3156-3165, 1986.
18. Cremer, T., Landegent, J., Bruckner, A., Scholl, H. P., Schardin, M., Hager, H. D., Devilee, P., Pearson, P., and van der Ploeg. M. Detection of chromosome aberrations in the human interphase nucleus by visualization of specific target DNAs with radioactive and non-radioactive in situ hybridization techniques: diagnosis of trisomy 18 with probe L1.84. Hum. Genet., 74: 346-352, 1986.
19. Waye, J. S., Greig, G., Durfy, S., England, S., Warburton, D., and Willard, H. F. Molecular characterization of chromosome-specific subsets of human alpha satellite DNA. Cytogenet. Cell Genet., 46: 712-720, 1987.
20. Inazawa, J., Saito, H., Ariyama, T., Abe, T., and Nakamura, Y. High-resolution cytogenetic mapping of 342 new cosmid markers including 43 RFLP markers on human chromosome 17 by fluorescence in situ hybridization. Genomics, 17: 153-162, 1993.