题名 | High-mobility group box 2 is associated with prognosis of glioblastoma by promoting cell viability, invasion, and chemotherapeutic resistance |
作者 | |
发表日期 | 2013-09 |
发表期刊 | NEURO-ONCOLOGY 影响因子和分区 |
语种 | 英语 |
原始文献类型 | Article |
关键词 | glioblastoma high-mobility group box 2 prognosis invasion temozolomide |
其他关键词 | BREAST-CANCER ; MATRIX METALLOPROTEINASES ; TISSUE INHIBITORS ; HEPATOCELLULAR-CARCINOMA ; ADJUVANT TEMOZOLOMIDE ; INCREASED EXPRESSION ; PROTEINS ; CISPLATIN ; HMGB1 ; METHYLATION |
摘要 | The expression profile of high-mobility group box 2 (HMGB2) in patients with glioblastoma multiforme (GBM) and its clinical signature with underlying mechanisms were not fully explored. HMGB2 protein levels were measured in 51 GBM patients by immunohistochemical studies. To clarify the precise role of HMGB2 on cell invasion and viability of 3 GBM cell lines, we did in vitro and in vivo analyses with lentivirus vectors and small interfering RNA. Transwell invasion assays and wound-healing assays were used to analyze the invasion of GBM cells. Expression of p53 and matrix metalloproteinase 2/tissue inhibitors of metalloproteinase 2 (MMP2/TIMP2) protein was analyzed by Western blot. HMGB2 protein expression was significantly higher in GBM than in controlled brain tissues (P .0001). HMGB2 overexpression was significantly correlated with shorter overall survival time, which was the only independent prognostic factor for overall survival in a multivariate analysis (P .017). HMGB2 knockdown by small interfering RNA decreased cell viability and invasion in vitro and significantly decreased tumor volume in vivo, which might be involved in the change of p53 expression and the balance of MMP2/TIMP2. Moreover, silencing of HMGB2 could significantly increase the sensitivity of GBM cells to temozolomide chemotherapy. Our present data suggest that HMGB2 expression is a significant prognostic factor and might play an important role in cell invasion and temozolomide-induced chemotherapeutic sensitivity of GBM. This study highlights the importance of HMGB2 as a novel prognostic marker and an attractive therapeutic target of GBM. |
资助项目 | Shanghai Science and Technology Research Program [10JC1402201]; National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [81271523]; Zhejiang Provincial Natural Science Foundation of ChinaNatural Science Foundation of Zhejiang Province [R2091137]; Zhejiang Provincial Program for the Cultivation of High-level Innovative Health Talents |
出版者 | OXFORD UNIV PRESS INC |
出版地 | CARY |
ISSN | 1522-8517 |
EISSN | 1522-8517 |
卷号 | 15期号:9页码:1264-1275 |
DOI | 10.1093/neuonc/not078 |
页数 | 12 |
WOS类目 | Oncology ; Clinical Neurology |
WOS研究方向 | Oncology ; Neurosciences & Neurology |
WOS记录号 | WOS:000323617500016 |
收录类别 | SCIE ; SCOPUS |
URL | 查看原文 |
PubMed ID | 23828241 |
SCOPUSEID | 2-s2.0-84883156379 |
自科自定义期刊分类 | T3(B)类 |
通讯作者地址 | [Zhou, Liang Fu]Department of Neurosurgery,Huashan Hospital,Fudan University,12 Wulumuqi Middle Road,China |
Scopus学科分类 | Oncology;Neurology (clinical);Cancer Research |
TOP期刊 | TOP期刊 |
引用统计 | |
文献类型 | 期刊论文 |
条目标识符 | https://kms.wmu.edu.cn/handle/3ETUA0LF/5293 |
专题 | 附属第一医院 |
通讯作者 | Zhou, Liang Fu |
作者单位 | 1.Department of Neurosurgery,Huashan Hospital,Fudan University,12 Wulumuqi Middle Road,China; 2.Department of Neurosurgery,First Affiliated Hospital of Wenzhou Medical College,China |
第一作者单位 | 附属第一医院 |
推荐引用方式 GB/T 7714 | Wu, Zhe Bao,Cai, Lin,Lin, Shao Jian,et al. High-mobility group box 2 is associated with prognosis of glioblastoma by promoting cell viability, invasion, and chemotherapeutic resistance[J]. NEURO-ONCOLOGY,2013,15(9):1264-1275. |
APA | Wu, Zhe Bao., Cai, Lin., Lin, Shao Jian., Xiong, Zhen Kun., Lu, Jiang Long., ... & Zhou, Liang Fu. (2013). High-mobility group box 2 is associated with prognosis of glioblastoma by promoting cell viability, invasion, and chemotherapeutic resistance. NEURO-ONCOLOGY, 15(9), 1264-1275. |
MLA | Wu, Zhe Bao,et al."High-mobility group box 2 is associated with prognosis of glioblastoma by promoting cell viability, invasion, and chemotherapeutic resistance".NEURO-ONCOLOGY 15.9(2013):1264-1275. |
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