Association between small heat shock protein B11 and the prognostic value of MGMT promoter methylation in patients with high-grade glioma

被引:28
作者
Cheng, Wen [1 ,6 ]
Li, Mingyang [4 ,5 ,6 ]
Jiang, Yang [1 ,6 ]
Zhang, Chuanbao [5 ,6 ]
Cai, Jinquan [2 ,6 ]
Wang, Kuanyu [3 ,6 ]
Wu, Anhua [1 ,6 ]
机构
[1] China Med Univ, Hosp 1, Dept Neurosurg, Nanjing St 155, Shenyang 110001, Peoples R China
[2] Harbin Med Univ, Affiliated Hosp 2, Harbin, Peoples R China
[3] Dalian Med Univ, Affiliated Hosp 1, Dalian, Peoples R China
[4] Capital Med Univ, Beijing Tiantan Hosp, Beijing, Peoples R China
[5] Beijing Neurosurg Inst, Beijing, Peoples R China
[6] Chinese Glioma Cooperat Grp, Beijing, Peoples R China
基金
国家高技术研究发展计划(863计划); 中国国家自然科学基金;
关键词
HSPB11; prognosis; MGMT promoter methylation; glioma; oncology; ALPHA-B-CRYSTALLIN; CELL-DEATH; EXPRESSION; TEMOZOLOMIDE; APOPTOSIS; MUTATION; IDH1; CHEMOTHERAPY; RADIOTHERAPY; ACTIVATION;
D O I
10.3171/2015.5.JNS142437
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
OBJECTIVE This study investigated the role and prognostic value of heat shock proteins (HSPs) in glioma. METHODS Data from 3 large databases of glioma samples (Chinese Glioma Genome Atlas, Repository for Molecular Brain Neoplasia Data, and GSE16011), which contained whole-genome messenger RNA microarray expression data and patients' clinical data, were analyzed. Immunohistochemical analysis was performed to validate protein expression in another set of 50 glioma specimens. RESULTS Of 28 HSPs, 11 were overexpressed in high-grade glioma (HGG) compared with low-grade glioma. A univariate Cox analysis revealed that HSPB11 has significant prognostic value for each glioma grade, which was validated by a Kaplan-Meier survival analysis. HSPB11 expression was associated with poor prognosis and was independently correlated with overall survival (OS) in HGG. This study further explored the combined role of HSPB11 and other molecular markers in HGG, such as isocitrate dehydrogenase 1 (IDH1) mutation and O-6-methylguanine-DNA methyltransferase (MGMT) promoter methylation status. HSPB11 expression was able to refine the prognostic value of IDH1 mutation in patients with HGG. However, when combined with MGMT promoter methylation status, among patients with a methylated MGMT promoter, those with lower levels of HSPB11 expression had longer OS and progression-free survival than patients with higher levels of HSPB11 expression or with an unmethylated MGMT promoter. Moreover, within the MGMT promoter methylation group, patients with low levels of HSPB11 expression were more sensitive to combined radioche-motherapy than those with high levels of HSPB11 expression, which may explain why some patients with HGG with a methylated MGMT promoter show tolerance to radiochemotherapy. CONCLUSIONS HSPB11 was identified as a novel prognostic marker in patients with HGG. Together with MGMT promoter methylation status, HSPB11 expression can predict outcome for patients with HGG and identify those who would most benefit from combined radiochemotherapy.
引用
收藏
页码:7 / 16
页数:10
相关论文
共 48 条
[1]   EXPRESSION OF ALPHA-B-CRYSTALLIN IN HUMAN BRAIN-TUMORS [J].
AOYAMA, A ;
STEIGER, RH ;
FROHLI, E ;
SCHAFER, R ;
VONDEIMLING, A ;
WIESTLER, OD ;
KLEMENZ, R .
INTERNATIONAL JOURNAL OF CANCER, 1993, 55 (05) :760-764
[2]   In search of the molecular mechanism by which small stress proteins counteract apoptosis during cellular differentiation [J].
Arrigo, AP .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2005, 94 (02) :241-246
[3]   Analysis of the IDH1 codon 132 mutation in brain tumors [J].
Balss, Joerg ;
Meyer, Jochen ;
Mueller, Wolf ;
Korshunov, Andrey ;
Hartmann, Christian ;
von Deimling, Andreas .
ACTA NEUROPATHOLOGICA, 2008, 116 (06) :597-602
[4]   Inhibition of cell death by a novel 16.2 kD heat shock protein predominantly via Hsp90 mediated lipid rafts stabilization and Akt activation pathway [J].
Bellyei, Szabolcs ;
Szigeti, Andras ;
Boronkai, Arpad ;
Pozsgai, Eva ;
Gomori, Eva ;
Melegh, Bela ;
Janaky, Tamas ;
Bognar, Zita ;
Hocsak, Eniko ;
Sumegi, Balazs ;
Gallyas, Ferenc, Jr. .
APOPTOSIS, 2007, 12 (01) :97-112
[5]   Preventing apoptotic cell death by a novel small heat shock protein [J].
Bellyei, Szabolcs ;
Szigeti, Andras ;
Pozsgai, Eva ;
Boronkai, Arpad ;
Gomori, Eva ;
Hocsak, Eniko ;
Farkas, Robert ;
Sumegi, Balazs ;
Gallyas, Ferenc, Jr. .
EUROPEAN JOURNAL OF CELL BIOLOGY, 2007, 86 (03) :161-171
[6]   Heat shock proteins in cancer: chaperones of tumorigenesis [J].
Calderwood, SK ;
Khaleque, MA ;
Sawyer, DB ;
Ciocca, DR .
TRENDS IN BIOCHEMICAL SCIENCES, 2006, 31 (03) :164-172
[7]   HDAC4, a prognostic and chromosomal instability marker, refines the predictive value of MGMT promoter methylation [J].
Cheng, Wen ;
Li, Mingyang ;
Cai, Jinquan ;
Wang, Kuanyu ;
Zhang, Chuanbao ;
Bao, Zhaoshi ;
Liu, Yanwei ;
Wu, Anhua .
JOURNAL OF NEURO-ONCOLOGY, 2015, 122 (02) :303-312
[8]   Small heat-shock proteins and their potential role in human disease [J].
Clark, JI ;
Muchowski, PJ .
CURRENT OPINION IN STRUCTURAL BIOLOGY, 2000, 10 (01) :52-59
[9]  
COLVIN M, 1981, CANCER TREAT REP, V65, P89
[10]  
Cornford PA, 2000, CANCER RES, V60, P7099