Immunohistochemical investigation of topoIIβ, H3K27me3 and JMJD3 expressions in medulloblastoma

被引:5
|
作者
Chen, Jing [1 ]
Zhao, Junxia [1 ]
Zhou, Xiaofen [2 ]
Liu, Shuang [3 ]
Yan, Yongxin [1 ]
Wang, Yanling [1 ]
Cao, Cuili [4 ]
Han, Shou [4 ]
Zhou, Najing [1 ]
Xu, Yannan [1 ]
Zhao, Juan [1 ]
Yan, Yunli [1 ]
Cui, Huixian [4 ]
机构
[1] Hebei Med Univ, Dept Cell Biol, Shijiazhuang 050017, Hebei, Peoples R China
[2] Second Peoples Hosp Zhengzhou, Dept Pathol, Zhengzhou 450000, Henan, Peoples R China
[3] Bethune Int Peace Hosp, Dept Pathol, Shijiazhuang 050000, Hebei, Peoples R China
[4] Hebei Med Univ, Dept Human Anat, Shijiazhuang 050017, Hebei, Peoples R China
关键词
Medulloblastoma; Classical subtypes of medulloblastoma; Desmoplastic subtype of medulloblastoma; Topoisomerase II beta; H3K27me3; JMJD3; INHIBITS NEURONAL DIFFERENTIATION; TOPOISOMERASE-II-BETA; NERVOUS-SYSTEM; CLASSIFICATION; ACTIVATION; TUMORS; SUBGROUPS; GENES;
D O I
10.1016/j.prp.2017.04.012
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Topoisomerase II beta (topoII beta) is a nuclear enzyme specifically expressed in.neurons, and plays an important role in the development of the cerebellum. To date, the expression of topoII beta protein in medulloblastoma (MB) has not been investigated. In this study, 16 MB specimens including 10 classical subtypes of MB and 6 desmoplastic subtypes of MB (DMB), along with 5 normal cerebellum samples, were obtained from clinics. With immunohistochemical staining, prominently expressed topoII beta was seen in normal cerebellar tissues, while there was no or less pronounced staining in classical MB cells. Interestingly, on comparing topoII beta expression in different regions of DMB samples, relatively high levels of topoII beta were revealed within nodules composed of differentiated neurocytic cells, which are known to predict a favorable clinical outcome for MB. We also examined the expression of two epigenetic factors, H3K27me3 and JMJD3 in the different tissues. Very high levels of H3K27me3 were found in all MB samples, except the intranodules of DMB, where JMJD3 expression was more prominent. Furthermore, a negative correlation between topollS and H3K27me3 in MB was revealed in this study. Thus, our data primarily indicate that topoII beta can be used to estimate neuronal differentiation in MB, and may serve as a target for improving the survival rates for this condition. We speculate that H3K27me3 repression of topoII beta at the transcriptional level may occur, although this needs to be verified using larger numbers of MB samples in future experiments. (C) 2017 Elsevier GmbH. All rights reserved.
引用
收藏
页码:975 / 981
页数:7
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