Loss of heterozygosity on chromosome 1 in human hepatoblastoma

International Journal of Cancer

Volumn 67, Issue 4, 1996, Pages 467-471

  Kraus, Jürgen A ^a,c   Albrecht, Steffen ^a,c,d   Wiestler, Otmar D ^a   Von Schweinitz, Dietrich ^b   Pietsch, Torsten ^a  

^a UNIVERSITY HOSPITAL BONN   (Germany)

^b HANNOVER MEDICAL SCHOOL   (Germany)

^c ALFRIED KRUPP KRANKENHAUS   (Germany)

^d MCGILL UNIVERSITY   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHILD; CHROMOSOME 1; CHROMOSOME ANALYSIS; CLINICAL ARTICLE; FEMALE; GENE AMPLIFICATION; HEPATOBLASTOMA; HETEROZYGOSITY; HUMAN; INFANT; LIVER CARCINOGENESIS; MALE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL;

ADOLESCENT; ADULT; ALLELES; CHILD; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 1; DNA, SATELLITE; FATHERS; FEMALE; GENETIC MARKERS; GENOMIC IMPRINTING; HEPATOBLASTOMA; HUMANS; LIVER NEOPLASMS; MALE; MIDDLE AGED; MOTHERS; POLYMERASE CHAIN REACTION;

EID: 0029787540     PISSN: 00207136     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1097-0215(19960807)67:4<467::AID-IJC1>3.0.CO;2-Q     Document Type: Article

References (33)

1. ALBRECHT, S., VON SCHWEINITZ, D., WAHA, A., KRAUS, J.A., VON DEIMLING, A. and PIETSCH, T., Loss of maternal alleles on chromosome arm 1 1p in hepatoblastoma. Cancer Res., 54, 5041-5044 (1994).
2. BARE, J.W., LEBO, R.V. and EPSTEIN, E.H. JR., Loss of heterozygosity at chromosome 1q22 in basal cell carcinomas and exclusion of the basal cell nevus syndrome gene from this site. Cancer Res., 52, 1494-1498 (1992).
3. BIÉCHE, I., CHAMPEME, M.H., MATIFAS, F., CROPP, C.S., CALLAHAN, R. and LIDERAU, R., Two distinct regions involved in 1p deletion in human primary breast cancer. Cancer Res., 53, 1990-1994 (1993).
4. BUDOWLE, B., CHAKRABORTY, R., GIUSTI, A., EISENBERG, A. and ALLEN, R., Analysis of the VNTR locus D1S80 by the PCR followed by high-resolution page. Amer. J. hum. Genet., 48, 137-144 (1991).
5. BYRNE, J.A., SIMMS, L.A., LITTLE, M.H., ALGAR, E.M. and SMITH, P.J., Three non-overlapping regions of chromosome arm 11p allele loss identified in infantile tumors of adrenal and liver. Genes Chromosomes Cancer, 8, 104-111 (1993).
6. CARON, H., and 12 OTHERS, Evidence for two tumour suppressor loci on chromosomal bands 1p35-36 involved in neuroblastoma: one probably imprinted, another associated with N-myc amplification. Hum. mol. Gen., 4, 535-539 (1995).
7. CHENG, J.M., HIEMSTRA, J.L., SCHNEIDER, S.S., NAUMOVA, A., CHEUNG, N.-K.V., COHN, S.L., DILLER, L., SAPIENZA, C. and BRODEUR, G.M., Preferential amplification of the paternal allele of the N-myc gene in human neuroblastoma. Nature (Genet.), 4, 191-194 (1993).
8. DIETRICH, W.F., LANDERS, E.S., SMITH, J.S., MOSER, A.R., GOULD, K.A., LUONGO, C., BORENSTEIN, N. and DOVE, W., Genetic identification of Mom-I, a major modifier locus affecting Min-induced intestinal neoplasia in the mouse. Cell, 75, 631-639 (1993).
9. DING, S.F., HABIB, N.A., DELHANTY, J.D.A., BOWLES, L., GRECO, L., WOOD, C., WILLIAMSON, R.C.N. and DOOLEY, J.S., Loss of heterozygosity on chromosomes 1 and 11 in carcinoma of the pancreas. Brit. J. Cancer, 65, 809-812 (1992).
10. DOUGLASS, E.C., GREEN, A.A., HAYES, F.A., ETCUBANAS, E., HOROWITZ, M. and WILIMAS, J.A., Chromosome I abnormalities: a common feature of pediatric solid tumors. J. nat. Cancer Inst., 75, 51-53 (1985).
11. DRACOPOLI, N.C., HARNETT, P., BALE, S.J., STANGER, B.Z., TUCKER, M.A., HOUSMAN, D.E. and KEFFORD, R.F., Loss of alleles from the distal short arm of chromosome 1 occurs late in melanoma tumour progression. Proc. nat. Acad. Sci. (Wash.), 86, 4614-4618 (1989).
12. ENGELSTEIN, M., HUDSON, T.J., LANE, J.M., LEE, M.K., LEVERONE, B., LANDES, G.M., PELTONEN, L., WEBER, J.L. and DRACOPOLI, N.C., A PCR-based linkage map of human chromosome 1. Genomics, 15, 251-258 (1993).
13. FONG, C.T., DRACOPOLI, N.C., WHITE, P.S., MERRILL, P.T., GRIFFITH, R.C., HOUSMAN, D.E. and BRODEUR, G.M., Loss of heterozygosity for the short arm of chromosome 1 in human neuroblastomas: correlation with N-myc amplification. Proc. nat. Acad. Sci. (Wash.), 86, 3753-3757 (1989).
14. FONG, C.T., WHITE, P.S., PETERSON, K., SAPIENZA, C., CAVENEE, W.K., KERN, S.E., VOGELSTEIN, B., CANTOR, A.B., LOOK, A.T. and BRODEUR, G.M., Loss of heterozygosity for chromosome 1 or 14 defines a subset of advanced neuroblastomas. Cancer Res., 52, 1780-1785 (1992).
15. HUGHES, L.J. and MICHELS, V.V., Risk of hepatoblastoma in familial adenomatouspolyposis. Amer. J. med. Genet., 43, 1023-1025 (1992).
16. KOUFOS, A., HANSEN, M.F., COPELAND, N.G., JENKINS, N.A., LAMPKIN, B.C. and CAVENEE, W.K., Loss of heterozygosity in three embryonal tumours suggests a common pathogenetic mechanism. Nature (Lond.), 316, 330-334 (1985).
17. KRAUS, J.A., KOOPMANN, J., KASKEL, P., MAINTZ, D., BRANDNER, S., SCHRAMM, J., LOUIS, D.N., WIESTLER, O.D. and VON DEIMLING, A., Shared allelic losses on chromosomes 1p and 19q suggest a common origin of oligodendroglioma and oligoastrocytoma. J. Neuropathol. exp. Neurol, 54, 91-95 (1995).
18. LEISTER, I., WEITH, A., BRUDERLEIN, S., CZIEPLUCH, C., KANGWANPONG, D., SCHLAG, P. and SCHWAB, M., Human colorectal cancer: high frequency of deletions at chromosome 1p35. Cancer Res., 50, 7232-7235 (1990).
19. LINDBLOM, A., RUTTLEDGE, M., COLLINS, V.P., NORDENSJOELD, M. and DUMANSKI, J.P., Chromosomal deletions in anaplastic meningio- mas suggest multiple regions outside chromosome 22 as important in tumor progression. Int. J. Cancer, 56, 354-357 (1994).
20. MANN, J.R., KASTHURI, N., RAAFAT, F., PINCOTT, J.R., PARKES, S.E., MUIR, K.R., INGRAM, L.C. and CAMERON, A.H., Malignant hepatic tumours in children: incidence, clinical features and aetiology. Paediatr. Perinat. Epidemiol., 4, 276-289 (1990).
21. MARIS, J.M., WHITE, P.S., BELTINGER, C.P., SULMAN, E.P., CASTLEBERRY, R.P., SHUSTER, J.J., LOOK, T.A. and BRODEUR, G.M., Significance of chromosome 1p loss of heterozygosity in neuroblastoma. Cancer Res., 55, 4664-4669 (1995).
22. MATHEW, S., MURTY, V.V.V.S., BOSL, G.J., and CHAGANTI, R.S.K., Loss of heterozygosity identifies multiple sites of allelic deletions on chromosome 1 in human male germ cell tumors. Cancer Res., 54, 6265-6269 (1994).
23. MOLEY, J.F., BROTHER, M.B., FONG, C.-T., WHITE, P.S., BAYLIN, S.B., NELKIN, B., WELLS, S.A. and BRODEUR, G.M., Consistent association of 1p loss of heterozygosity with pheochromocytomas from patients with multiple endocrine neoplasia type 2 syndromes. Cancer Res., 52, 770-774 (1992).
24. NISHIMURA, D.Y. and MURRAY, J.C., A tetranucleotide repeat for the F13B locus. Nucl. Acids Res., 20, 1167 (1992).
25. PATEL, M.S., MANKOO, B.S. and BRICKELL, P.M., A polymorphic microsatellite repeat is located close to the promoter region of the c-fgr proto-oncogene (FGR) at chromosome 1p36.2-p36.1. Hum. mol. Genet., 1, 65 (1992).
26. PERRY, D.J., Trinucleotide repeat polymorphism in the human antithrombin III (AT3) gene. Hum. mol. Genet., 2, 618 (1993).
27. PIETSCH, T., FONATSCH, C., ALBRECHT, S., MASCHEK, D., WOLF, H.K. and VON SCHWEINITZ, D., Characterization of the continuous cell line HepT1 derived from a human hepatoblastoma. Lab. Invest., 74, 809-818 (1996).
28. SANO, T., TSUJINO, T., YOSHIDA, K., NAKAYAMA, H., HARUMA, K., ITO, H., NAKAMURA, Y., KAJIYAMA, G. and TAHARA. E., Frequent loss of heterozygosity on chromosome 1q, 5q, and 17p in human gastric carcinomas. Cancer Res., 51, 2926-2931 (1991).
29. SIMON, D., KNOWLES, B.B. and WEITH, A., Abnormalities of chromosome 1 and loss of heterozygosity on 1p in primary hepatoblastomas. Oncogene, 6, 765-770 (1991).
30. WEINBERG, A.G. and FINEGOLD, M.J., Primary hepatic tumors of childhood. Hum. Pathol., 14, 512-537 (1983).
31. WEISSENBACH, J., GYAPAY, G., DIB, C., VIGNAL, A., MORISSETTE, J., MILLASSEAU, P., VAYSSEIX, G. and LATHROP, M., A second-generation linkage map of the human genome. Nature (Lond.), 359, 794-801 (1992).
32. WEITH, A., MARTINSSON, T., CZIEPLUCH, C., BRUDERLEIN, S., AMLER, L.C., BERTHOLD, F. and SCHWAB, M., Neuroblastoma consensus deletion maps to 1p36.1-2. Genes Chromosomes Cancer, 1, 159-166 (1989).
33. YEH, S.-H., CHEN, P.-J., CHEN, H.-L., LAI, M.-Y., WANG, C.-C. and CHEN, D.-S., Frequent genetic alterations at the distal region of chromosome 1p in human hepatocellular carcinomas. Cancer Res., 54, 4188-4192 (1994).