Genetic aberrations in glioblastoma multiforme: translocation of chromosome 10 in an O-2A-like cell line

被引:8
作者
Mao, X
Jones, TA
Tomlinson, I
Rowan, AJ
Fedorova, LI
Zelenin, AV
Mao, JI
Gutowski, NJ
Noble, M
Sheer, D
机构
[1] Imperial Canc Res Fund, Human Cytogenet Lab, London WC2A 3PX, England
[2] Imperial Canc Res Fund, Canc Genet Lab, London WC2A 3PX, England
[3] Russian Acad Sci, VA Engelhardt Mol Biol Inst, Moscow, Russia
[4] Genome Therapeut Corp, Genomics & Technol Dev, Waltham, MA 02154 USA
[5] Ludwig Inst Canc Res, London W1P 8BT, England
基金
英国惠康基金;
关键词
cytogenetics; FISH; molecular genetics; glioblastoma multiforme;
D O I
10.1038/sj.bjc.6690116
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We have examined the genetic aberrations in two near-diploid glioblastoma multiforme cell lines that appear to have arisen from different glial lineages. One cell line, Hu-O-2A/Gb1, expresses antigens and metabolic profiles characteristic of the oligodendrocyte-type-2 astrocyte (0-2A) lineage of the rat central nervous system. This line generates, in vitro, cells with characteristics of 0-2A progenitor cells, oligodendrocytes and astrocytes. The second cell line, IN1434, is derived from an astrocyte or a precursor cell restricted to astrocytic differentiation. in Hu-0-2A/Gb1 the sole homologue of chromosome 10 is disrupted at band 10p11-12.1 by translocation with chromosomes X and 15. The translocation breakpoint is localized between genetic markers D10S2103 and [D10S637, D10S1962, D10S355]. Other aberrations include a 5;14 translocation, deletion of the long and short arms of chromosome 16 and loss of one copy of the CDKN2 gene. IN1434 cells share some cytogenetic abnormalities with Hu-O-2A/Gb1 cells, despite their apparent derivation from a different biological origin, but also have translocations involving the long and short arms of chromosome 1 and the long arm of chromosome 7, and deletion of chromosome 13 at bands 13q12-21.
引用
收藏
页码:724 / 731
页数:8
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