2型神经纤维瘤病
生物
外显子
神经纤维瘤病
抑癌基因
基因
星形细胞瘤
22号染色体
癌变
癌症研究
胶质瘤
遗传学
染色体
作者
Mari‐Paz Rubio,Katia M. Correa,Vijaya Ramesh,Mia MacCollin,Lee B. Jacoby,Andreas von Deimling,James F. Gusella,David N. Louis
出处
期刊:PubMed
[National Institutes of Health]
日期:1994-01-01
卷期号:54 (1): 45-7
被引量:148
摘要
Ependymomas and astrocytomas commonly have allelic losses of chromosome 22q, which suggests the presence of a glioma tumor suppressor gene on 22q. A candidate tumor suppressor gene on 22q is the neurofibromatosis 2 (NF2) gene since NF2 patients have an increased susceptibility to ependymomas and astrocytomas. Using single strand conformation polymorphism analysis and direct DNA sequencing, we screened 8 ependymomas and 30 fibrillary astrocytomas from non-NF2 patients for mutations in the coding sequence and portions of the 3' untranslated region of the NF2 gene. Only one mutation was detected, a single base deletion in NF2 exon 7 from a spinal ependymoma, which had also lost the wild-type allele. These results suggest that the NF2 gene may be important in the formation of some ependymomas but the NF2 gene is probably not the critical chromosome 22q tumor suppressor gene involved in astrocytoma tumorigenesis.
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