A tumor suppressor locus in familial and sporadic chordoma maps to 1p36

International Journal of Cancer

Volumn 87, Issue 1, 2000, Pages 68-72

  Miozzo, Monica ^a   Dalprà, Leda ^a   Riva, Paola ^a   Volontè, Marinella ^a   Macciardi, Fabio ^b   Pericotti, Sergio ^c   Tibiletti, M Grazia ^d   Cerati, Michele ^d   Rohde, Klaus ^e   Larizza, Lidia ^a   Fuhrman Conti, A Maria ^a  

^a UNIVERSITY OF MILAN   (Italy)

^b UNIVERSITY OF TORONTO   (Canada)

^c OSPEDALI RIUNITI   (Italy)

^d UNIVERSITY OF INSUBRIA   (Italy)

^e MAX DELBRÜCK CENTER FOR MOLECULAR MEDICINE   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; ASTROCYTOMA; CANCER SUSCEPTIBILITY; CHORDOMA; CLIVUS; CYTOGENETICS; GENE LOCUS; GENE MAPPING; GENE REARRANGEMENT; HETEROZYGOSITY LOSS; HUMAN; HUMAN TISSUE; KARYOTYPE; MULTIGENE FAMILY; PRIORITY JOURNAL; TUMOR SUPPRESSOR GENE;

ADULT; ASTROCYTOMA; BRAIN NEOPLASMS; CEREBELLAR NEOPLASMS; CHILD; CHILD, PRESCHOOL; CHORDOMA; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 1; CRANIAL FOSSA, POSTERIOR; DINUCLEOTIDE REPEATS; FEMALE; GENES, TUMOR SUPPRESSOR; GENETIC MARKERS; HAPLOTYPES; HUMANS; LINKAGE (GENETICS); LOSS OF HETEROZYGOSITY; MALE; PEDIGREE;

EID: 0034084439     PISSN: 00207136     EISSN: None     Source Type: Journal    
DOI: 10.1002/1097-0215(20000701)87:1<68::AID-IJC10>3.0.CO;2-V     Document Type: Article

References (25)

1. BELLO, M.J., LEONE, P.E., VAQUERO, J., DE CAMPOS, J.M., KUSAK, M.E. and SARASA, J.L., Allelic status of chromosome 1 in neoplasms of the nervous system. Cancer Genet. Cytogenet., 83, 160-164 (1995).
2. BUTLER, M.G., DAHIR, G.A., HEDGES, L.K., JULIAO, S.F., SCIADINI, M.F. and SCHWARTZ, H.S., Cytogenetic, telomere, and telomerase studies in five surgically managed lumbosacral chordomas. Cancer Genet. Cytogenet., 85, 51-57 (1995).
3. CHETTY, R., LEVIN, C.V. and KALAN, M.R., Chordoma: a 20-year clinicopathologic review of the experience at Groote Schuur Hospital, Cape Town. J. Surg. Oncol., 46, 261-264 (1991).
4. COTTINGAM, R.W., IDURY, R.M. and SCHAFFE, A.A., Faster sequential genetic linkage computation. Amer. J. Hum. Genet., 53, 252-263 (1993).
5. DALPRÀ, L., MALGARA, R., MIOZZO, M., RIVA, P., VOLONTE, M., LARIZZA, L. and FUHRMAN CONTI, A.M., First cytogenetic study of a recurrent familial chordoma of the clivus. Int. J. Cancer, 81, 24-30 (1999).
6. FECHNER, R.E. and MILLS, S.E., Tumors of the bones and joints. Atlas of tumor pathology (3rd series). Fascicle 8, pp. 239-244, Armed Forces Institute of Pathology, Washington D.C. (1993).
7. FOOTE, R.F., ABLIN, G. and HALL, W., Chordoma in siblings. Calif. Med., 88, 383-386 (1958).
8. GIBBS, M. and 14 OTHERS, Evidence for a rare prostate cancer susceptibility locus at chromosome 1p36. Amer. J. hum. Genet., 64, 776-787 (1999).
9. GOEL, A., NADKARNI, T.D. and KIRTANE, M.V., Clival chordoma in an infant. J. Postgrad. Med., 42, 51-53 (1996).
10. HIGUCHI, R., Rapid, efficient DNA extraction from cells or blood. Perkin Elmer Cetus. Amplification. 2, 1-3 (1989).
11. KERR, W.A., ALLEN, K.L., HAYNES, D.R. and SELLARS, S.L., Familial nasopharyngeal chordoma. S. Afr. med. J., 49, 1584 (1975).
12. KORCZAK, J.F., KELLEY, M.J., ALLIKIAN, K.A., SHAH, A.A., GOLDSTEIN, A.M. and PARRY, D.M., Genomic screening for linkage in a family with autosomal dominant chordoma. Amer. J. hum. Genet., 61, A400 (1997).
13. KRUGLYAK, L., DALY, M.J., REEVE-DALY, M.P. and LANDER, E.S., Parametric and nonparametric linkage analysis: a unified multipoint approach. Amer. J. hum. Genet., 58, 1347-1363 (1996).
14. LATHROP, G.M., LALOUEL, J.M., JULIER, C. and OTT, J., Strategies for multilocus linkage analysis in humans. Proc. nat. Acad. Sci. (Wash.), 81, 3443-3446 (1984).
15. MERTENES, F., KREICBERGS, A., RYDHOLM, A., WILLEN, H., CARLEN, B., MITELMAN, F. and MANDAHL, N., Clonal chromosome aberrations in three sacral chordomas. Cancer Genet. Cytogenet., 73, 147-151 (1994).
16. O'CONNELL, J.R. and WEEKS, D.E., The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recording and fuzzy inheritance. Nature (Genet.), 11, 402-408 (1995).
17. PROBST, E.N., ZANELLA, F.E. and VORTMEYER, A.O., Congenital clivus chordoma. Amer. J. Neuroradiol. 14, 537-539 (1993).
18. ROHDE, K., TEARE, M.D., SANTIBAÑEZ-KOREF, M., Analysis of genetic linkage and somatic loss of heterozygosity in affected pairs of first-degree relatives. Amer. J. Hum. Genet., 61, 418-422 (1997).
19. ROHDE, K., TEARE, M.D., SCHERNECK, S. and SANTIBAÑEZ-KOREF, M. A program using loss of constitutional heterozygosity data to ascertain the location of predisposing genes in cancer families. Hum. Hered., 45, 337-345 (1995).
20. RUMPEL, C.A., POWELL S.M. and MOSKALUK C.A., Mapping of genetic deletions on the long arm of the chromosome 4 in human esophageal adenocarcinomas. Amer. J. Pathol., 154, 1329-1334 (1999).
21. STEPANEK, J., CATALDO, S.A., EBESOLD, M.J., LINDOR, N.M., JENKINS, R.B., WEINSHENKER, B.J. and RUBENSTEIN, R.L., Familial chordoma with probable autosomal dominant inheritance. Amer. J. Med. Genet., 75, 335-336 (1998).
22. SCHWAB, M., PRAML, C. and AMLER, L.C., Genomic instability in 1p and human malignancies. Genes Chromosomes Cancer, 16, 211-229 (1996).
23. VAN ROY, N., JAUCH, A., VAN GELE, M., LAUREYS, G., VERSTEEG, R., DE PAEPE, A. and CREMER, T., Comparative genomic hybridization analysis of human neuroblastoma: detection of distal 1p deletions and further molecular genetic characterization of neuroblastoma cell lines. Cancer Genet. Cytogenet., 97, 135-142 (1997).
24. WATKINS, C., WARNE, D., KELSELL, D., BECKMANN, J., NYBERG, K. and SPURR, N., The use of PCR and ethidium bromide staining to detect length variation in short repeat units. Technique, 3, 175-178 (1991).
25. WERNICKE, C., THIEL, G., LOZANOVA, T., VOGEL, S. and WITKOWSKI, R., Numerical aberration of chromosomes 1, 2, and 7 in astrocytoma studied by interphase cytogenetic. Genes Chromosomes Cancer, 19, 6-13 (1997).