Correlation between apoptosis, proliferation and bcl-2 expression in malignant non-Hodgkin's lymphoma.

S W Kiberu, J H Pringle, S Sobolewski, P Murphy, I Lauder
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引用次数: 26

Abstract

Aim-To investigate whether clinical features of non-Hodgkin's lymphomas, at the time of first biopsy, correlate with studies of cell proliferation and cell death as well as with the level of bcl-2 expression.Methods-Bcl-2 expression, determined by immunocytochemistry, was compared with cell proliferation, measured using in situ hybridisation for histone mRNA, and cell death by apoptosis, measured using in situ end labelling for DNA cleavage.Results-Histone mRNA staining gave a labelling index of 30% of cells for reactive germinal centres, 5.2-13.5% of cells for low grade non-Hodgkin's lymphoma and 12.1-50.5% of cells for high grade non-Hodgkin's lymphoma. In situ end labelling gave a labelling index of 5.0-10.0% of cells for reactive germinal centres, 1.0-3.7% of cells for low grade non-Hodgkin's lymphoma and 4.7-13.5% of cells for high grade non-Hodgkin's lymphoma. There was a positive correlation between apoptotic index and proliferation index. More cases of low grade than high grade non-Hodgkin's lymphoma expressed bcl-2. There was no correlation between apoptotic index and bcl-2 expression for high grade non-Hodgkin's lymphoma.Conclusions-The molecular mechanisms controlling cell proliferation and death in non-Hodgkin's lymphoma are complex, probably involving a range of genes, including bcl-2. A better understanding of resistance to cell death is needed if the clinical goal of tailoring cancer treatment to individual tumours is to be achieved.

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恶性非霍奇金淋巴瘤细胞凋亡、细胞增殖与bcl-2表达的关系
目的:探讨非霍奇金淋巴瘤在第一次活检时的临床特征是否与细胞增殖和细胞死亡以及bcl-2表达水平相关。方法:用免疫细胞化学方法测定bcl -2的表达,并与细胞增殖(用组蛋白mRNA原位杂交法测定)和细胞凋亡(用DNA切割原位末端标记法测定)进行比较。结果:组蛋白mRNA染色显示30%的细胞为反应性生发中心,5.2-13.5%的细胞为低级别非霍奇金淋巴瘤,12.1-50.5%的细胞为高级别非霍奇金淋巴瘤。原位末端标记的阳性生发中心细胞的标记指数为5.0-10.0%,低级别非霍奇金淋巴瘤细胞的标记指数为1.0-3.7%,高级别非霍奇金淋巴瘤细胞的标记指数为4.7-13.5%。细胞凋亡指数与细胞增殖指数呈正相关。低级别非霍奇金淋巴瘤表达bcl-2的病例多于高级别非霍奇金淋巴瘤。高分级非霍奇金淋巴瘤细胞凋亡指数与bcl-2表达无相关性。结论:控制非霍奇金淋巴瘤细胞增殖和死亡的分子机制是复杂的,可能涉及一系列基因,包括bcl-2。如果要实现针对个别肿瘤的癌症治疗的临床目标,就需要更好地了解细胞死亡的耐药性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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