Syndecan-4 as a biomarker to predict clinical outcome for glioblastoma multiforme treated with WT1 peptide vaccine.
Syndecan-4 as a biomarker to predict clinical outcome for glioblastoma multiforme treated with WT1 peptide vaccine.
复制标题
Syndecan-4 作为生物标志物来预测 WT1 肽疫苗治疗的多形性胶质母细胞瘤的临床结果。
DOI:
10.4155/fsoa-2015-0008
复制
发表时间:
2016-12
影响因子:
2.5
通讯作者:
Sugiyama H
中科院分区:
文献类型:
--
作者:
Takashima S;Oka Y;Fujiki F;Morimoto S;Nakajima H;Nakae Y;Nakata J;Nishida S;Hosen N;Tatsumi N;Mizuguchi K;Hashimoto N;Oji Y;Tsuboi A;Kumanogoh A;Sugiyama H
In cancer immunotherapy, biomarkers are important for identification of responsive patients. This study was aimed to find biomarkers that predict clinical outcome of WT1 peptide vaccination. Candidate genes that were expressed differentially between long- and short-term survivors were identified by cDNA microarray analysis of peripheral blood mononuclear cells that were extracted from 30 glioblastoma patients (discovery set) prior to vaccination and validated by quantitative RT-PCR using discovery set and different 23 patients (validation set). SDC-4 mRNA expression levels distinguished between the long- and short-term survivors: 1-year survival rates were 64.0 and 18.5% in SDC4-low and -high patients, respectively. SDC-4 is a novel predictive biomarker for the efficacy of WT1 peptide vaccine. Recently, cancer immunotherapies are becoming a standard therapeutic option. To improve their efficacy, identification of biomarkers is important to select responsive patients. In this study, we identified SDC-4 as a biomarker to predict clinical outcome using peripheral blood mononuclear cells obtained from patients with glioblastoma, a malignant brain tumor, who were treated with WT1 peptide vaccine. With 30 samples of peripheral blood mononuclear cells prior to vaccination, 32 candidate genes were filtrated by microarray, and finally only SDC-4 was validated by RT-PCR using another 23 samples. Accordingly, 1-year survival rates were 64.0 and 18.5% in SDC4-low and -high patients, respectively.