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[垂体腺瘤染色体畸变的初步研究]

[Preliminary study of chromosome aberrations in pituitary adenoma].

作者信息

Wang Qing, Hui Guo-zhen, Lin Yu-chang, Lu Xiao-jie, Yu Wen-hua, Wu Si-rong, Wu Zhi-yuan

机构信息

Department of Neurosurgery, Affiliated Wuxi Second Hospital of Nanjing Medical University, Wuxi 214001, P. R. China.

出版信息

Ai Zheng. 2002 Oct;21(10):1120-3.

Abstract

BACKGROUND & OBJECTIVE: Pituitary adenoma is one of the most common intracranial benign tumor. This study was designed to seek the most suitable method for cytogenetic study of pituitary adenoma(PA), and then to analyze the genetic change of PA cell.

METHODS

Twenty-five samples of primary PA were examined by R-banding through direct preparation(DP) and short-term culture(STC) to analyze genomic alterations.

RESULTS

A karyotype of 17 samples was identified in 25 PAs by using the DP, whereas there was a karyotype of 21 samples by using the STC. An abnormal clonal karyotype was observed in 11 samples processed by the DP, however only 3 of 25 samples when processed by the STC. The common chromosomal alterations included gains of chromosomes X(6/25), 7(4/25), 8(2/25), 5(2/25) as well as losses of chromosomes 11(5/25), 9(4/25), 13(3/25), and the latter was observed predominantly in invasive PAs.

CONCLUSIONS

DP is one of the most suitable methods for the cytogenetic study of PA. There were multiple regions of chromosomes with copy number changes in PA including gains of chromosomes X, 7, 8, and losses of chromosomes 11, 9, 13. However, structural chromosome aberrations are not common. The loss of chromosome and the abnormality of structure may have some correlation with the biologic behavior of PA.

摘要

背景与目的

垂体腺瘤是最常见的颅内良性肿瘤之一。本研究旨在探寻垂体腺瘤(PA)细胞遗传学研究的最适宜方法,进而分析PA细胞的基因变化。

方法

采用R显带技术,通过直接制片(DP)和短期培养(STC)对25例原发性PA样本进行检测,以分析基因组改变。

结果

25例PA中,采用DP法鉴定出17例样本的核型,采用STC法鉴定出21例样本的核型。DP法处理的11例样本观察到异常克隆核型,而STC法处理的25例样本中仅3例观察到异常克隆核型。常见的染色体改变包括X(6/25)、7(4/25)、8(2/25)、5(2/25)号染色体增多以及11(5/25)、9(4/25)、13(3/25)号染色体减少,后者主要见于侵袭性PA。

结论

DP是PA细胞遗传学研究的最适宜方法之一。PA存在多个染色体区域的拷贝数改变,包括X、7、8号染色体增多以及11、9、13号染色体减少。然而,染色体结构畸变并不常见。染色体丢失及结构异常可能与PA的生物学行为存在一定关联。

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