Romani M, Muresu R, Volpi E V, Rozzo C, Marchi J M, Casciano I
Istituto Nazionale per la Ricerca sul Cancro, IST, Porto Conte Research and Training Laboratories, Alghero, Italy.
J Neurooncol. 1997 Jan;31(1-2):41-7. doi: 10.1023/a:1005725112688.
Specific chromosomal aberrations might indicate the position of genes responsible for a particular disease. Neuroblastoma is characterized by frequent deletions and/or rearrangements of the subtelomeric 1p region which, accordingly, is believed to host one or more oncosuppressor gene(s) directly or indirectly involved in the development of this and other tumors. Identification of these genes could be facilitated if cell lines with well characterized interstitial deletions or reciprocal translocations could be available for application of positional cloning strategies. In the present report we present additional and novel molecular data on three well established neuroblastoma cell lines (NLF, NMB and NGP). In one of these we have identified two sites that might be good candidates for hosting oncosuppressor genes; one of these is flanked by the D1S47 and ENO1 loci while the other is distal to the A12M2 locus.
特定的染色体畸变可能表明负责某种特定疾病的基因位置。神经母细胞瘤的特征是亚端粒1p区域频繁缺失和/或重排,因此,该区域被认为直接或间接承载一个或多个与这种及其他肿瘤发生相关的抑癌基因。如果能获得具有明确特征的间质缺失或相互易位的细胞系,用于定位克隆策略,那么这些基因的鉴定将会更容易。在本报告中,我们展示了关于三种成熟的神经母细胞瘤细胞系(NLF、NMB和NGP)的更多新分子数据。在其中一个细胞系中,我们鉴定出了两个可能是抑癌基因所在的良好候选位点;其中一个位点位于D1S47和ENO1基因座之间,而另一个位点在A12M2基因座的远端。