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原发性肠道非霍奇金淋巴瘤小细胞和大细胞亚型中的细胞更新参数

Cell turnover parameters in small and large cell varieties of primary intestinal non-Hodgkin's lymphoma.

作者信息

Gisbertz I A, Schouten H C, Bot F J, Arends J W

机构信息

Department of Internal Medicine, University Hospital Maastricht, The Netherlands.

出版信息

Cancer. 1998 Jul 1;83(1):158-65. doi: 10.1002/(sici)1097-0142(19980701)83:1<158::aid-cncr21>3.0.co;2-v.

Abstract

BACKGROUND

In contrast to primary gastric lymphoma, primary intestinal lymphoma is an uncommon condition with a poorer outcome, perhaps due to differences in its pathogenesis. In this study, the authors analyzed the roles of proliferation and apoptosis in the pathogenesis of intestinal lymphoma.

METHODS

Fifty-one cases of intestinal non-Hodgkin's lymphoma (NHL) (10 small B-cell mucosa-associated lymphoid tissue [MALT] NHLs, 12 large B-cell MALT NHLs, 18 large B-cell NHLs, 2 small T-cell NHLs, 7 large T-cell NHLs, and 2 mantle cell NHLs) were studied for the immunohistochemical expression of MIB-1 and the TUNEL assay as well as the expression of bcl-2 and p53, both of which are regulatory gene products involved in apoptosis.

RESULTS

The median proliferation index (PI) was 37.3%, and the median apoptotic index (AI) was 1.10%. The respective values of PI and AI were 5.8% and 0.06% in small B-cell MALT lymphoma, 52.8% and 0.24% in large B-cell MALT lymphoma, 58.85% and 1.36% in large B-cell lymphoma, 30.9% and 1.93% in mantle cell lymphoma, 18.13% and 1.25% in small T-cell lymphoma, and 43.4% and 1.93% in large T-cell lymphoma. In an analysis of B-cell NHL only (with mantle cell NHL excluded), proliferative and apoptotic indices were positively correlated (correlation coefficient=0.563, P < 0.001). Furthermore, high bcl-2 expression was inversely correlated with both PI and AI. Expression of p53 was observed in 8 cases (1 small cell lymphoma and 7 large cell lymphomas).

CONCLUSIONS

Small cell lymphomas had low AI and PI values, whereas large cell lymphomas had high AI and PI values. Apoptosis and proliferation were positively correlated, and higher expression of bcl-2 was associated with lower rates of apoptosis.

摘要

背景

与原发性胃淋巴瘤不同,原发性肠道淋巴瘤是一种罕见疾病,预后较差,这可能与其发病机制的差异有关。在本研究中,作者分析了增殖和凋亡在肠道淋巴瘤发病机制中的作用。

方法

对51例肠道非霍奇金淋巴瘤(NHL)(10例小B细胞黏膜相关淋巴组织[MALT] NHL、12例大B细胞MALT NHL、18例大B细胞NHL、2例小T细胞NHL、7例大T细胞NHL和2例套细胞NHL)进行研究,检测MIB-1的免疫组化表达、TUNEL检测以及bcl-2和p53的表达,这两者均为参与凋亡的调节基因产物。

结果

增殖指数(PI)中位数为37.3%,凋亡指数(AI)中位数为1.10%。小B细胞MALT淋巴瘤的PI和AI值分别为5.8%和0.06%,大B细胞MALT淋巴瘤为52.8%和0.24%,大B细胞淋巴瘤为58.85%和1.36%,套细胞淋巴瘤为30.9%和1.93%,小T细胞淋巴瘤为18.13%和1.25%,大T细胞淋巴瘤为43.4%和1.93%。仅对B细胞NHL(排除套细胞NHL)进行分析时,增殖指数和凋亡指数呈正相关(相关系数=0.563,P<0.001)。此外,bcl-2高表达与PI和AI均呈负相关。8例(1例小细胞淋巴瘤和7例大细胞淋巴瘤)检测到p53表达。

结论

小细胞淋巴瘤的AI和PI值较低,而大细胞淋巴瘤的AI和PI值较高。凋亡与增殖呈正相关,bcl-2高表达与凋亡率较低相关。

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