Non-random trisomies of chromosomes 5, 8 and 12 in the prolactinoma sub- type of pituitary adenomas: Conventional cytogenetics and interphase fish study

International Journal of Cancer

Volumn 89, Issue 2, 2000, Pages 344-350

  Finelli, Palma ^a   Giardino, Daniela ^a   Rizzi, Nicoletta ^a   Buiatiotis, Simona ^a   Virduci, Tiziana ^a   Franzin, Alberto ^b   Losa, Marco ^b   Larizza, Lidia ^a,c  

^a ISTITUTO AUXOLOGICO ITALIANO   (Italy)

^b SAN RAFFAELE HOSPITAL   (Italy)

^c UNIVERSITY OF MILAN   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGED; ARTICLE; CHROMOSOME 12; CHROMOSOME 5; CHROMOSOME 8; CYTOGENETICS; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE FREQUENCY; GENETIC ANALYSIS; HUMAN; HUMAN CELL; HUMAN TISSUE; HYPOPHYSIS ADENOMA; INTERPHASE; KARYOTYPE; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; PROLACTINOMA; TRISOMY; GENETICS; HYPOPHYSIS TUMOR; MIDDLE AGED;

ADULT; AGED; CHROMOSOMES, HUMAN, PAIR 12; CHROMOSOMES, HUMAN, PAIR 5; CHROMOSOMES, HUMAN, PAIR 8; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; MIDDLE AGED; PITUITARY NEOPLASMS; PROLACTINOMA; TRISOMY;

EID: 0034185985     PISSN: 00207136     EISSN: None     Source Type: Journal    
DOI: 10.1002/(sici)1097-0215(20000501)86:3<344::aid-ijc7>3.0.co;2-8     Document Type: Article

References (20)

1. ARCHIDIACONO, N., ANTONACCI, R., MARZELLA, R., FINELLI, P., LONOCE, A. and ROCCHI, M., Comparative mapping of human alphoid sequences in great apes using fluorescence in situ hybridization. Genomics, 25, 477-484 (1995).
2. BALDINI, A., ROCCHI, M., ARCHIDIACONO, N., MILLER, O.J. and MILLER, D.A., A human alpha satellite DNA sub-set specific for chromosome 12. Amer. J. Hum. genet., 46, 784-788 (1990).
3. BETTIO, D., RIZZI, N., GIARDINO, D., PERSANI, L., PECORI-GIRALDI, F., LOSA, M. and LARIZZA, L., Cytogenetic study of pituitary adenomas. Cancer Genet. Cytogenet., 98, 131-136 (1997).
4. BRITO-BABAPULLE, V and ATKIN N.B., Breakpoints in chromosome-1 abnormalities of 218 human neoplasms. Cancer Genet. Cytogenet., 4, 215-225 (1981).
5. CAPRA, E., RINDI, G., SANTI, G., POMPEI SPINA, M. and SCAPPATICCI, S., Chromosome abnormalities in a case of pituitary adenoma. Cancer Genet. Cytogenet., 68, 140-142 (1993).
6. CAPRA, E., SCAPPATCCI, S. and POMPEI SPINA, M., Chromosome abnormalities in tumor and lymphocyte cultures from patients with pituitary adenomas. Cancer Genet. Cytogenet., 84, 89 (1995).
7. CHUMAKOV, I.M., RIGAULT, P., LE GALL, I., BELLANE-CHANTELOT, C. and COHEN, D., A YAC contig map of the human genome. Nature (Lond.), 377 (Suppl. 28), 175-297 (1995).
8. DANIELY, M., AVIRAM, A., ADAMS, E.F., BUCHFELDER, M., BARKAI, G., FAHLBUSCH, R., GOLDMAN, B. and FRIEDMAN, E., Comparative genomic hybridization analysis of non-functioning pituitary tumors. J. clin. Endocrinol. Metab., 83, 1801-1805 (1998).
9. DIETRICH, C.U., PANDIS, N., BJERRE, P., SCHRODER, D. and HEIMS, S., Simple numerical chromosome aberration in two pituitary adenomas. Cancer Genet. Cytogenet., 69, 118-121 (1993).
10. KOVACS, K. and HORVATH, E., Atlas of tumor pathology, Fascicle 21, II series, AFP1, Washington (1986).
11. LICHTER, P. and CREMER, T., Chromosome analysis by non-isotopic in situ hybridization. In: D.E. Rooney and B.H. Czipolkowski (eds), Human cytogenetics - a practical approach, pp. 157-192, Oxford University Press, Oxford (1992).
12. LICHTER, P., TANG CHANG, C.-J., CALL, K., HERMANSON, G., EVANS, G.A., HOUSMAN, D. and WARD, D.C., High-resolution mapping of human chromosomes 11 by in situ hybridization with cosmid clones. Science, 247, 64-69 (1990).
13. MARK, J., DAHLENFORS, R. and WEDELL, B., Impact of in vitro technique used on the cytogenetic patterns in pleomorphic adenomas. Cancer Genet. Cytogenet., 95, 9-15 (1997).
14. MITELMAN, F., ISCN (1995): an international system for human cytogenetic nomenclature, Karger, Basel (1995).
15. MITELMAN, F., JOHANSSON, B., MANDHAL, N. and MERTENS, F., Clinical significance of cytogenetic findings in solid tumors. Cancer Genet. Cytogenet., 95, 1-8 (1997a).
16. MITELMAN, F., MERTENS, F. and JOHANSSON, B., A breakpoint map of recurrent chromosomal rearrangements in human neoplasia. Nature Genet., 15 (Special number), 417-474 (1997b).
17. REY, J.A., BELLO, M.J., DE CAMPOS, J.M., KUSAK, E., MARTINEZ-CASTRO, P., and BENITEZ, J., A case of pituitary adenoma with 58 chromosomes. Cancer Genet. Cytogenet., 23, 171-174 (1986).
18. SCHOENMAKERS, E.F.P.M., WANSCHURA, S., MOLS, R., BULLERDIEK, J., VAN DEN BERGHE, H. and VAN DE VEN, W.J.M., Recurrent rearrangements in the high-mobility-group-protein gene, HMGI-C, in benign mesenchymal tumors. Nature Genet., 10, 436-444 (1995).
19. SHIMON, I. and MELMED, S., Genetic basis of endocrine disease. Pituitary-tumor pathogenesis. J. clin. Endocrinol Metab., 82, 1675-1680 (1997).
20. Kip1 gene and trisomy 12 in a sub-set of human pituitary adenomas. J. clin. Endocrinol. Metab., 82, 3141-3147 (1997).