人类恶性黑色素瘤细胞系的细胞遗传学研究。

M Yin, M A Yoshida, A Tonomura, T Kasuga
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引用次数: 0

摘要

对3例恶性黑色素瘤患者的6株细胞系进行了细胞遗传学研究。模态染色体数目在半三倍体到超四倍体之间,染色体数目和结构都有畸变。在染色体1、6和7上最常观察到畸变。1q的缺失在所有细胞系中一致存在,而在病例1的两个细胞系中观察到6q的缺失。易位t (Y;6)和t(6;?)发生在病例3的一个细胞系中。7号染色体拷贝数增加是病例2细胞系的一个特征。由于恶性黑色素瘤中EGF受体的表达与7号染色体剂量增加呈正相关,并且EGFR基因已被定位到7p12-p13带,这一现象可能对恶性黑色素瘤的增殖具有重要意义。本研究的结果与先前发表的文献数据基本一致,表明在黑色素瘤的发展过程中存在特异性的非随机染色体病变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cytogenetic studies of human malignant melanoma cell lines.

Cytogenetic studies were performed on six cell lines derived from three patients suffering from malignant melanomas. The modal chromosome numbers were in the hypotriploid to hypertetraploid ranges and both the numerical and structural aberrations of chromosomes were found. Aberrations were most frequently observed in chromosomes 1, 6 and 7. Deletion of 1q was consistently present in all cell lines, while loss of 6q was observed in two cell lines of case 1. Translocations t (Y; 6) and t (6;?) occurred in one cell line from case 3. An increased number of copies of chromosome 7 was a characteristic feature of the cell lines from case 2. Since positive correlation between the expression of EGF receptors and an increased dosage of chromosome 7 has been reported for malignant melanomas and the gene for EGFR has been mapped to band 7p12-p13, this phenomenon might be of importance for the proliferation of malignant melanoma. The findings of the present study are generally in agreement with the data previously published in the literature, indicating the existence of specific non-random chromosome lesions during melanoma development.

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