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MYC 基因拷贝数增加与弥漫性大 B 细胞淋巴瘤中 mRNA 水平升高相关。

Increased MYC gene copy number correlates with increased mRNA levels in diffuse large B-cell lymphoma.

机构信息

Department of Pathology, University of Arizona, 1501 N Campbell Avenue, PO Box 245043, Tucson, AZ 85724-5043, USA.

出版信息

Haematologica. 2010 Apr;95(4):597-603. doi: 10.3324/haematol.2009.012864.

Abstract

BACKGROUND

Translocations involving the MYC gene and increased MYC mRNA levels are associated with poor outcome in diffuse large B-cell lymphoma. However, the presence of increased MYC gene copy number and/or polysomy of chromosome 8 have not been previously described.

DESIGN AND METHODS

Utilizing dual color chromogenic in situ hybridization, we investigated MYC gene copy and chromosome 8 centromere numbers in 52 cases of diffuse large B-cell lymphoma. Cases were divided into those with "increased" or "not increased" MYC gene copy number for comparison with MYC mRNA levels, Ki-67 values, and survival.

RESULTS

Increased MYC gene copy number was present in 38% of cases. Overall, the average MYC mRNA level was 2398 (range, 342 - 9783) and the percentage of nuclei positive for Ki-67 was 57.5% (range, 20-87%). Within the group with increased MYC copy number, the MYC mRNA values ranged from 816 to 5912 (average, 2843) and the Ki-67 values ranged from 23% to 83% (average, 57%). Within the group with not increased MYC copy number, MYC mRNA values ranged from 342 to 9783 (average, 2118) and the Ki-67 values ranged from 20% to 87% (average, 58%). There was a statistically significant relationship between increased MYC gene copy number and increased MYC mRNA (P=0.034) and a trend toward a relationship between increased mRNA and higher Ki-67 values.

CONCLUSIONS

This is the first report that low level copy number increases are common in diffuse large B-cell lymphoma and that these changes correlate with MYC mRNA in a statistically significant manner. MYC copy number changes are an additional possible molecular mechanism that may result in increased mRNA and, likely, high proliferation and poor outcome.

摘要

背景

涉及 MYC 基因的易位和 MYC mRNA 水平升高与弥漫性大 B 细胞淋巴瘤的不良预后相关。然而,MYC 基因拷贝数增加和/或 8 号染色体三体的存在以前尚未被描述。

设计和方法

利用双色显色原位杂交,我们研究了 52 例弥漫性大 B 细胞淋巴瘤中 MYC 基因拷贝数和 8 号染色体着丝粒数。将病例分为 MYC 基因拷贝数“增加”或“未增加”的病例进行比较,比较指标包括 MYC mRNA 水平、Ki-67 值和生存情况。

结果

38%的病例存在 MYC 基因拷贝数增加。总体而言,平均 MYC mRNA 水平为 2398(范围为 342-9783),Ki-67 阳性核的百分比为 57.5%(范围为 20-87%)。在 MYC 拷贝数增加的组内,MYC mRNA 值范围为 816 至 5912(平均 2843),Ki-67 值范围为 23%-83%(平均 57%)。在 MYC 拷贝数未增加的组内,MYC mRNA 值范围为 342 至 9783(平均 2118),Ki-67 值范围为 20%-87%(平均 58%)。MYC 基因拷贝数增加与 MYC mRNA 增加之间存在统计学显著关系(P=0.034),且 mRNA 增加与 Ki-67 值升高之间存在趋势关系。

结论

这是首次报道在弥漫性大 B 细胞淋巴瘤中常见低水平拷贝数增加,并且这些变化与 MYC mRNA 以统计学显著的方式相关。MYC 拷贝数变化是一种可能的分子机制,可能导致 mRNA 增加,以及高增殖和不良预后。

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