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人视网膜母细胞瘤细胞中13号染色体缺失:与肿瘤发生的相关性。

A deleted chromosome no. 13 in human retinoblastoma cells: relevance to tumorigenesis.

作者信息

Balaban-Malenbaum G, Gilbert F, Nichols W W, Hill R, Shields J, Meadows A T

出版信息

Cancer Genet Cytogenet. 1981 Apr;3(3):243-50. doi: 10.1016/0165-4608(81)90091-1.

Abstract

In this report of banded karyotypes prepared after short-term culture (72 hr) from human retinoblastoma tumor tissue, on del(13)(pter leads to q14:) chromosome and one normal chromosome #13 were found in all of the metaphases examined. Similar deletions (always involving 13q14) have previously been described in the somatic cells of individuals with one form of retinoblastoma. In the present case, however, the constitutional karyotype is normal. The presence of tumors in both eyes suggests that this is the genetic form of retinoblastoma, even though the patient's family history is negative for this tumor. The normal constitutional karyotype argues that the chromosome deletion occurred as a postzygotic event. The modal chromosome number of the tumor cells is 47 and rearrangements involving chromosomes #2, #17, and #20 were also identified.

摘要

在这份关于从人视网膜母细胞瘤肿瘤组织短期培养(72小时)后制备的带型核型报告中,在所有检查的中期相中均发现一条del(13)(pter→q14:)染色体和一条正常的13号染色体。先前在患有某种形式视网膜母细胞瘤的个体的体细胞中已描述过类似的缺失(总是涉及13q14)。然而,在本病例中,染色体组核型是正常的。双眼出现肿瘤表明这是视网膜母细胞瘤的遗传形式,尽管患者的家族史对该肿瘤呈阴性。正常的染色体组核型表明染色体缺失是合子后事件。肿瘤细胞的众数染色体数为47,还鉴定出涉及2号、17号和20号染色体的重排。

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