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pmid:28977840

Autophagy-related gene expression is an independent prognostic indicator of glioma.

Huixue Zhang · Xiaoyan Lu · Ning Wang · Jianjian Wang · Yuze Cao · Tianfeng Wang · Xueling Zhou · Yang Jiao · Lei Yang · Xiaokun Wang · Lin Cong · Jianlong Li · Jie Li · He-Ping Ma · Yonghui Pan · Shangwei Ning · Lihua Wang

Oncotarget · 2017 doi:10.18632/oncotarget.17719

Paper

complete

Experiment

complete

Data

partial

Analysis

partial

Execution

absent

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pmid:28977840
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title
Autophagy-related gene expression is an independent prognostic indicator of glioma.
doi
10.18632/oncotarget.17719
pmid
28977840
authors array · 17 items
[0]
Huixue Zhang
[1]
Xiaoyan Lu
[2]
Ning Wang
[3]
Jianjian Wang
[4]
Yuze Cao
[5]
Tianfeng Wang
[6]
Xueling Zhou
[7]
Yang Jiao
[8]
Lei Yang
[9]
Xiaokun Wang
[10]
Lin Cong
[11]
Jianlong Li
[12]
Jie Li
[13]
He-Ping Ma
[14]
Yonghui Pan
[15]
Shangwei Ning
[16]
Lihua Wang
journal
Oncotarget
year
2017
abstract
In this study, we identified 74 differentially expressed autophagy-related genes in glioma patients. Analysis using a Cox proportional hazard regression model showed that MAPK8IP1 and SH3GLB1, two autophagy-related genes, were associated with the prognostic signature for glioma. Glioma patients from the CGGA batches 1 and 2, GSE4412 and TCGA datasets could be divided into high- and low-risk groups with different survival times based on levels of MAPK8IP1 and SH3GLB1 expression. The autophagy-related signature was an independent predictor of survival outcomes in glioma patients. MAPK8IP1 overexpression and SH3GLB1 knockdown inhibited glioma cell proliferation, migration and invasion, and improved Temozolomide sensitivity. These findings suggest autophagy-related genes like MAPK8IP1 and SH3GLB1 could be potential therapeutic targets in glioma.
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The Kaplan-Meier method was used to estimate overall survival. The differences in survival between high- and the low-risk patients was analyzed by two-sided log-rank test.
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The Kaplan-Meier method was used to estimate overall survival. The differences in survival between high- and the low-risk patients was analyzed by two-sided log-rank test.
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The mRNA microarray of glioma samples and their clinical information was obtained from the Chinese Glioma Genome Atlas (CGGA, http://www.cgga.org.cn/) [47]. The mRNA microarray of CGGA, produced by Agilent Whole Human Genome Array was divided into two batches.
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sections[14] "The Chinese Glioma Genome Atlas datasets" paragraph 2
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The mRNA microarray of glioma samples and their clinical information was obtained from the Chinese Glioma Genome Atlas (CGGA, http://www.cgga.org.cn/) [47]. The mRNA microarray of CGGA, produced by Agilent Whole Human Genome Array was divided into two batches.
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The study used Cox proportional hazard regression to identify an autophagy-related prognostic signature comprising MAPK8IP1 and SH3GLB1, and evaluated it in CGGA batches 1 and 2, GSE4412, and TCGA glioma datasets.
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Autophagy-related signature is an independent predictor of glioma
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The mRNA microarray of glioma samples and their clinical information was obtained from the Chinese Glioma Genome Atlas (CGGA, http://www.cgga.org.cn/) [47]. The mRNA microarray of CGGA, produced by Agilent Whole Human Genome Array was divided into two batches.
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PMID 28977840 full text
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atients. MAPK8IP1 overexpression and SH3GLB1 knockdown inhibited glioma cell proliferation, migrati
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IP1) + 0.311×(expression value of SH3GLB1)]. Patients with high risk scores had poor clinical outcomes.
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related with overall survival (P<0.05). Each patient was assigned a risk score based on the expression level o
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The Kaplan-Meier method was used to estimate overall survival. The differences in survival between high- and the low-risk patients was analyzed by two-sided log-rank test.
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Complete file
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