JMJD2B as a potential diagnostic immunohistochemical marker for hepatocellular carcinoma: A tissue microarray-based study

被引:16
作者
Lu, Jeng-Wei [1 ]
Ho, Yi-Jung [2 ,3 ]
Lin, Liang-In [1 ,4 ]
Huang, Yen-Chi [5 ]
Yeh, Kun-Tu [6 ,7 ]
Lin, Yu-Hsiang [9 ]
Lin, Yueh-Min [6 ,7 ,8 ]
Tzeng, Tsai-Yu [9 ]
机构
[1] Natl Taiwan Univ, Dept Clin Lab Sci & Med Biotechnol, Taipei 10764, Taiwan
[2] Natl Def Med Ctr, Inst Prevent Med, Taipei, Taiwan
[3] Natl Def Med Ctr, Grad Inst Life Sci, Taipei, Taiwan
[4] Natl Taiwan Univ Hosp, Dept Lab Med, Taipei, Taiwan
[5] Hsin Sheng Jr Coll Med Care & Management, Dept Styling & Cosmetol, Taoyuan, Taiwan
[6] Changhua Christian Hosp, Dept Pathol, Changhua, Taiwan
[7] Chung Shan Med Univ, Sch Med, Taichung, Taiwan
[8] Jen Teh Jr Coll Med, Dept Med Technol, Miaoli, Taiwan
[9] Natl Yang Ming Univ, VYM Genome Res Ctr, Taipei 112, Taiwan
关键词
Diagnostic marker; lmmunohistochemistry; JMJD2B; Tissue microarray; Human hepatocellular carcinoma; HISTONE DEMETHYLASE JMJD2B; PROGNOSTIC MOLECULAR MARKERS; CELL-PROLIFERATION; HYPOXIA; METHYLATION; TARGETS; FAMILY;
D O I
10.1016/j.acthis.2014.10.002
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The purpose of this study was to examine JMJD2B expression in human hepatocellular carcinoma (HCC) and elucidate relationships between various expression patterns and clinicopathological parameters of HCC patients. Immunohistochemical techniques were performed to detect JMJD2B expression in a tissue microarray from patients with breast, cerebrum, colon, esophagus, kidney, liver, lung, prostate, stomach, and uterus cancers. We performed immunohistochemical staining of a multiple tissue array to examine the expression profile of JMJD2B. Our results demonstrate that JMJD2B protein levels were upregulated in malignant human tumors, including breast, colon, liver, and lung. Immunohistochemistry staining examination of liver tumor tissue microarray revealed that the expression of JMJD2B is significant according to the histological grade and TNM stage of liver tumor. Moreover, JMJD2B was also correlated with Ki-67 expression in HCC samples. These results reveal that JMJD2B is dramatically unregulated in HCC, making it a potential diagnostic marker for the further development of HCC treatment therapies. (C) 2014 Elsevier GmbH. All rights reserved.
引用
收藏
页码:14 / 19
页数:6
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