Finnegan M C, Hammond D W, Hancock B W, Goyns M H
Department of Clinical Oncology, Sheffield University Medical School, United Kingdom.
Leuk Lymphoma. 1995 Aug;18(5-6):511-4. doi: 10.3109/10428199509059653.
We have examined a series of non-Hodgkin's lymphomas (NHL) for evidence of expression of the MYC gene family. Northern blot analysis of RNA samples derived from 11 non-malignant reactive lymphoid tissues and 33 NHL was used to investigate expression of MYC, MYCL and MYCN. As expected MYC expression was detected in all samples. The levels of MYC expression were quantified by densitometry and appeared to be 3-8 fold higher in high grade NHL than in the low grade NHL or non-malignant lymphoid tissue. No expression of MYCL was detected in any sample. Expression of MYCN was however observed in one sample, which had been diagnosed as a T-cell high grade NHL. A detailed cytogenetic analysis of this sample proved difficult to obtain but, by using fluorescence in-situ hybridization (FISH), we were able to demonstrate that on one of the chromosomes 2 the MYCN gene was localised to a translocation breakpoint region. It therefore appears that in NHL it is possible for MYCN, like MYC in Burkitt lymphoma, to be activated as a result of a chromosome translocation event.
我们检测了一系列非霍奇金淋巴瘤(NHL),以寻找MYC基因家族表达的证据。采用Northern印迹分析法对来自11个非恶性反应性淋巴组织和33个NHL的RNA样本进行检测,以研究MYC、MYCL和MYCN的表达情况。正如预期的那样,在所有样本中均检测到MYC表达。通过密度测定法对MYC表达水平进行定量分析,结果显示高级别NHL中的MYC表达水平比低级别NHL或非恶性淋巴组织中的高3 - 8倍。在任何样本中均未检测到MYCL表达。然而,在一个被诊断为T细胞高级别NHL的样本中观察到了MYCN表达。对该样本进行详细的细胞遗传学分析很困难,但是通过使用荧光原位杂交(FISH)技术,我们能够证明在其中一条2号染色体上,MYCN基因定位于一个易位断点区域。因此,在NHL中,与伯基特淋巴瘤中的MYC一样,MYCN有可能因染色体易位事件而被激活。