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涉及1p和17q的易位是人类神经母细胞瘤细胞反复出现的基因改变。

Translocation involving 1p and 17q is a recurrent genetic alteration of human neuroblastoma cells.

作者信息

Savelyeva L, Corvi R, Schwab M

机构信息

German Cancer Research Center, Department of Cytogenetics, Heidelberg.

出版信息

Am J Hum Genet. 1994 Aug;55(2):334-40.

Abstract

Human neuroblastoma cells often are monosomic for the distal portion of 1p (1p36). We report that the deleted 1p material in cells of neuroblastoma lines is preferentially replaced by material from chromosome 17, resulting from an unbalanced 1;17 translocation. Chromosome 17 often acquires instability, followed by the integration of fragments into various marker chromosomes. As a consequence, 17q material can increase over 17p material. The nonrandom frequency of 1;17 translocations appears to indicate an as-yet-undefined contribution to neuroblastoma development.

摘要

人类神经母细胞瘤细胞通常在1号染色体短臂远端(1p36)存在单体性。我们报告称,神经母细胞瘤细胞系中缺失的1p物质优先被17号染色体的物质所取代,这是由不平衡的1;17易位导致的。17号染色体常常获得不稳定性,随后片段整合到各种标记染色体中。因此,17号染色体长臂物质相对于短臂物质会增加。1;17易位的非随机频率似乎表明其对神经母细胞瘤发展有尚未明确的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d4b/1918368/64f9cf369dcd/ajhg00041-0124-a.jpg

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