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多形性胶质母细胞瘤中的基因畸变:一种O-2A样细胞系中的10号染色体易位。

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

作者信息

Mao X, Jones T A, Tomlinson I, Rowan A J, Fedorova L I, Zelenin A V, Mao J I, Gutowski N J, Noble M, Sheer D

机构信息

Human Cytogenetics Laboratory, Imperial Cancer Research Fund, London, UK.

出版信息

Br J Cancer. 1999 Feb;79(5-6):724-31. doi: 10.1038/sj.bjc.6690116.

Abstract

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-O-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.

摘要

我们检测了两个近二倍体多形性胶质母细胞瘤细胞系中的基因畸变情况,这两个细胞系似乎源自不同的神经胶质谱系。一个细胞系Hu-O-2A/Gb1表达大鼠中枢神经系统少突胶质细胞-2型星形胶质细胞(O-2A)谱系特有的抗原和代谢谱。该细胞系在体外可产生具有O-2A祖细胞、少突胶质细胞和星形胶质细胞特征的细胞。第二个细胞系IN1434源自星形胶质细胞或局限于星形胶质细胞分化的前体细胞。在Hu-O-2A/Gb1中,10号染色体的唯一同源物在10p11-12.1带处因与X染色体和15号染色体易位而中断。易位断点定位于遗传标记D10S2103与[D10S637、D10S1962、D10S355]之间。其他畸变包括5号和14号染色体易位、16号染色体长短臂缺失以及CDKN2基因一个拷贝的丢失。IN1434细胞尽管明显源自不同的生物学起源,但与Hu-O-2A/Gb1细胞有一些细胞遗传学异常,不过也有涉及1号染色体长短臂和7号染色体长臂的易位,以及13号染色体13q12-21带处的缺失。

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本文引用的文献

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Characterization of a flow-sorted human chromosome 10 cosmid library by FISH.
Cytogenet Cell Genet. 1996;74(4):266-71. doi: 10.1159/000134432.

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