Comparative genomic hybridization analysis of genetic alterations associated with malignant progression of meningioma.

作者: Satoshi Ozaki , Takafumi Nishizaki , Haruhide Ito , Kohsuke Sasaki

DOI: 10.1023/A:1006086723607

关键词:

摘要: Little is known about genetic alterations during malignant progression of meningioma. We used comparative genomic hybridization (CGH) in 20 patients (13 with typical, 4 atypical and 3 anaplastic meningiomas) to investigate the pathway underlying development Typical meningiomas displayed only a few changes such as monosomy 22. Anaplastic manifested more aberrations than typical meningiomas, frequently exhibiting losses 1p, 2p, 6q, chromosome 10 14q, gain 20q, addition The average number alteration sites each patient meningioma was significantly less those (p < 0.01) 0.05). showed chromosomal seen together other aberrations. These CGH findings suggest that 20q are implicated

参考文章(50)
Bernard F. Schneider, Vandana Shashi, Chris von Kap-herr, Wendy L. Golden, Loss of chromosomes 22 and 14 in the malignant progression of meningiomas: A comparative study of fluorescence in situ hybridization (FISH) and standard cytogenetic analysis Cancer Genetics and Cytogenetics. ,vol. 85, pp. 101- 104 ,(1995) , 10.1016/0165-4608(95)00154-9
T. Cremer, M. Kiessling, R. G. Weber, F. K. Albert, C. Sommer, Clinically distinct subgroups of glioblastoma multiforme studied by comparative genomic hybridization. Laboratory Investigation. ,vol. 74, pp. 108- 119 ,(1996)
Ruth Wellenreuther, John M. Tew, Andreas Waha, Anil G. Menon, Jeffrey J. Larson, Ronald E. Warnick, Peter Kaskel, Andreas von Deimling, Matthias Simon, Allelic Losses on Chromosomes 14, 10, and 1 in Atypical and Malignant Meningiomas: A Genetic Model of Meningioma Progression Cancer Research. ,vol. 55, pp. 4696- 4701 ,(1995)
Susan Mathew, VVVS Murty, George J Bosl, RSK Chaganti, None, Loss of heterozygosity identifies multiple sites of allelic deletions on chromosome 1 in human male germ cell tumors. Cancer Research. ,vol. 54, pp. 6265- 6269 ,(1994)
J. F. Gusella, R. Wellenreuther, A. Von Deimling, O. D. Wiestler, Vijaya Ramesh, D. N. Louis, J. Schramm, A. G. Menon, J. A. Kraus, D. Lenartz, Analysis of the neurofibromatosis 2 gene reveals molecular variants of meningioma. American Journal of Pathology. ,vol. 146, pp. 827- 832 ,(1995)
Nordenskjöld M, Dumanski Jp, Collins Vp, Rouleau Ga, Molecular Genetic Analysis of Chromosome 22 in 81 Cases of Meningioma Cancer Research. ,vol. 50, pp. 5863- 5867 ,(1990)
Manfred Schwab, Peter Schlag, Ilona Leister, Silke Brüderlein, Celina Cziepluch, Daoroong Kangwanpong, Andreas Weith, Human Colorectal Cancer: High Frequency of Deletions at Chromosome 1p35 Cancer Research. ,vol. 50, pp. 7232- 7235 ,(1990)
Takafumi Nishizaki, Sandy DeVries, Karen Chew, William H. Goodson, Britt-Marie Ljung, Ann Thor, Frederic M. Waldman, Genetic alterations in primary breast cancers and their metastases: Direct comparison using modified comparative genomic hybridization Genes, Chromosomes and Cancer. ,vol. 19, pp. 267- 272 ,(1997) , 10.1002/(SICI)1098-2264(199708)19:4<267::AID-GCC9>3.0.CO;2-V
A Kallioniemi, O. Kallioniemi, D Sudar, D Rutovitz, J. Gray, F Waldman, D Pinkel, Comparative Genomic Hybridization for Molecular Cytogenetic Analysis of Solid Tumors Science. ,vol. 258, pp. 818- 821 ,(1992) , 10.1126/SCIENCE.1359641
A. Al Saadi, F. Latimer, M. Madercic, T. Robbins, Cytogenetic studies of human brain tumors and their clinical significance. II. Meningioma Cancer Genetics and Cytogenetics. ,vol. 26, pp. 127- 141 ,(1987) , 10.1016/0165-4608(87)90140-3