Fine deletion mapping of chromosome 8p in non-small-cell lung carcinoma

International Journal of Cancer

Volumn 81, Issue 6, 1999, Pages 854-858

  Lerebours, Florence ^a   Olschwang, Sylviane ^a   Thuille, Bénédicte ^a   Schmitz, Annette ^b   Fouchet, Pierre ^b   Buecher, Bruno ^c   Martinet, Nadine ^d   Galateau, Françoise ^e   Thomas, Gilles ^a  

^a INSERM   (France)

^b INSTITUT DE RADIOPROTECTION ET DE SÛRETÉ NUCLÉAIRE   (France)

^c CHU de Nantes   (France)

^d CHU NANCY BRABOIS   (France)

^e CHU CÔTE DE NACRE   (France)

Author keywords

[No Author keywords available]

Indexed keywords

CYTOKERATIN; DNA;

ARTICLE; CHROMOSOME 8P; CHROMOSOME DELETION; CHROMOSOME MAP; CONTROLLED STUDY; FLOW CYTOMETRY; GENETIC POLYMORPHISM; HUMAN; HUMAN CELL; HUMAN TISSUE; LUNG CARCINOMA; MAJOR CLINICAL STUDY; POLYPLOIDY; PRIORITY JOURNAL; TUMOR SUPPRESSOR GENE;

CARCINOMA, NON-SMALL-CELL LUNG; CENTROMERE; CHROMOSOME DELETION; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 8; GENES, TUMOR SUPPRESSOR; GENETIC MARKERS; HUMANS; LOSS OF HETEROZYGOSITY; LUNG NEOPLASMS; MICROSATELLITE REPEATS; PLOIDIES; POLYMERASE CHAIN REACTION; POLYMORPHISM, GENETIC;

EID: 0033010514     PISSN: 00207136     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1097-0215(19990611)81:6<854::AID-IJC3>3.0.CO;2-1     Document Type: Article

References (22)

1. BJORKQVIST, A.M., TAMMILEHTO, L., NORDLING, S., NURMINEN, M., ANTTILA, S., MATTSON, K. and KNUUTILA, S., Comparison of DNA copy-number changes in malignant mesothelioma, adenocarcinoma and large-cell anaplastic carcinoma of the lung. Brit. J. Cancer, 77, 260-269 (1998).
2. BOIGE, V., LAURENT-PUIG, P., FOUCHET, P., FLÉIOU, J.F., MONGES, G., BEDOSSA, P., BIOULAC-SAGE, P., CAPRON, F., SCHMITZ, A., OLSCHWANG, S. and THOMAS, G., Concerted nonsyntenic allelic losses in hyperploid hepatocellular carcinoma as determined by a high resolution allelotype. Cancer Res., 57, 1986-1990 (1997).
3. BOVA, G.S., MACGROGAN, D., LEVY, A., PIN, S.S., BOOKSTEIN, R. and ISAACS, W.B., Physical mapping of chromosome 8p22 markers and their homozygous deletion in a metastatic prostate cancer. Genomics, 35, 46-54 (1996).
4. COOPER, C.A., BUBB, V.J., SMITHSON, N., CARTER, R.L., GLEDHILL, S., LAMB, D., WYLLIE, A.H. and CAREY, F.A., Loss of heterozygosity at 5q21 in non-small cell lung cancer: a frequent event but without evidence of APC mutation. J. Pathol., 180, 33-37 (1996).
5. FIELD, J.K., NEVILLE, E.M., STEWART, M.P., SWIFT, A., LILOGLOU, T., RISK, J.M., ROSS, H., GOSNEY, J.R. and DONNELLY, R.J., Fractional allele loss data indicate distinct genetic populations in the development of non-small-cell lung cancer. Brit. J. Cancer, 74, 1968-1974 (1996).
6. FONG, K.M., ZIMMERMAN, P.V. and SMITH, P.J., Correlation of loss of heterozygosity at 11p with tumour progression and survival in non-small cell lung cancer. Genes Chromosomes Cancer, 10, 183-189 (1994).
7. FUJINO, M., DOSAKA-AKITA, H., HARADA, M., HIROUMI, H., KINOSHITA, I., AKIE, K. and KAWAKAMI, Y., Prognostic significance of p53 and ras p21 expression in non-small cell lung cancer. Cancer, 76, 2457-2463 (1995).
8. FUJIWARA, Y., OHATA, H., EMI, M., OKUI, K., KOYAMA, K., TSUCHIYA, E., NAKAJIMA, T., MONDEN, M., MORI, T., KURIMASA, A., OSHIMURA, M. and NAKAMURA, Y., A 3Mb physical map of the chromosome region 8p21.3-p22, including a 600-kb region commonly deleted in human hepatocellular carcinoma, colorectal cancer and non-small cell lung cancer. Genes Chromosomes Cancer, 10, 7-14 (1994).
9. FUJIWARA, Y., OHATA, H., KUROKI, T., KOYAMA, K., TSUCHIYA, E., MONDEN, M. and NAKAMURA, Y., Isolation of candidate tumor suppressor gene on chromosome 8p21.3-p22 that is homologous to an extracellular domain of the PDGF-receptor beta gene. Oncogene, 10, 891-895 (1995).
10. GUSTAFSON, C.E., WILSON, P.J., LUKEIS, R., BAKER, E., WOOLLATT, E., ANNAB, L., HAWKE, L., BARRETT, J.C. and CHENEVIX-TRENCH, G., Functional evidence for a colorectal cancer tumor suppressor gene at chromosome 8p22-23 by monochromosome transfer. Cancer Res., 56, 5238-5245 (1996).
11. HAUSTERMANS, K., HOFLAND, I., RAMAEKERS, M., IVANYI, D., BALM, A.J., GEBOES, K., LERUT, T., VAN DER SCHUEREN, E. and BEGG, A.C., Enrichment of tumor cells for cell kinetic analysis in human tumor biopsies using cytokeratin gating. Radiother. Oncol, 41, 237-248 (1996).
12. KISHIMOTO, Y., SUGIO, K., HUNG, J.Y., VIRMANI, A.K., MACINTIRE, D.D., MINNA, J.D. and GAZDAR, A.F., Allele-specific loss in chromosome 9p loci in preneoplastic lesions accompanying non-small-cell lung cancers. J. nat. Cancer Inst., 87, 1224-1229 (1995).
13. LEERS, M.P., THEUNISSEN, P.H., SCHUTTE, T.B. and RAMAEKERS, F.C., Bivariate cytokeratin/DNA flow cytometric analysis of paraffin-embedded samples from colorectal carcinomas. Cytometry, 21, 101-107 (1995).
14. MACGROGAN, D., LEVY, A., BOVA, S., ISAACS, W.B. and BOOKSTEIN, R., Structure and methylation-associated silencing of a gene within a homozygous deleted region of human chromosome band 8p22. Genomics, 35, 55-65 (1996).
15. OHATA, H., EMI, M., FUJIWARA, Y., HIGASHINO, K., NAKAGAWA, K., FUTAGAMI, R., TSUCHIYA, E. and NAKAMURA, Y., Deletion mapping of the short arm of chromosome 8 in non-small cell lung carcinoma. Genes Chromosomes Cancer, 7, 85-88 (1993).
16. OKAMOTO, A., HUSSAIN, S.P., HAGIWARA, K., SPILLARE, E.A., RUSIN, M.R., DEMETRICK, D.J., SERRANO, M., HANNON, G.J., SHISEKI, M., ZARIWALA, M. and HARRIS, C.C., Mutations in the p161NK4/MTS1/CDKN2, p151NK4B/ MTS2, and p18 genes in primary and metastatic lung cancer. Cancer Res., 55, 1448-1451 (1995).
17. SHISEKI, M., KOHNO, T., ADACHI, J., OKAZAKI, T., OTSUKA, T., MIZOGUCHI, H., NOGUCHI, M., HIROHASHI, S. and YOKOTA, J., Comparative allelotype of early and advanced stage non-small cell lung carcinomas. Genes Chromosomes Cancer, 17, 71-77 (1996).
18. SOZZI, G. and 13 OTHERS, The FHIT gene 3p14.2 is abnormal in lung cancer. Cell, 85, 17-26 (1996).
19. TAKLE, L.A. and KNOWLES, M.A., Deletion mapping implicates two tumor suppressor genes on chromosome 8p in the development of bladder cancer. Oncogene, 12, 1083-1087 (1996).
20. TAMURA, K., ZHANG, X., MURAKAMI, Y., HIROHASHI, S., XU, H.J., HU, S.X., BENEDICT, W.F. and SEKIYA, T., Deletion of three distinct regions on chromosome 13q in human non-small-cell lung cancer. Int. J. Cancer, 74, 45-49 (1997).
21. THIBERVILLE, L., PAYNE, P., VIELKINDS, J., LERICHE, J., HORSMAN, D., NOUVET, G., PALCIC, B. and LAM, S., Evidence of cumulative gene losses with progression of premalignant epithelial lesions to carcinoma of the bronchus. Cancer Res., 55, 5133-5139 (1995).
22. YAREMKO, M.L., KUTZA, C., LYZAK, J., MOCK, R., RECANT, W.M. and WESTBROOK, C. A., Loss of heterozygosity from the short arm of chromosome 8 is associated with invasive behaviour in breast cancer. Genes Chromosomes Cancer, 16, 189-195 (1996).