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pmid:36009075

Elevated Hexose-6-Phosphate Dehydrogenase Regulated by OSMR-AS1/hsa-miR-516b-5p Axis Correlates with Poor Prognosis and Dendritic Cells Infiltration of Glioblastoma.

Yi-Bin Zhang · Shu-Fa Zheng · Lin-Jie Ma · Peng Lin · Huang-Cheng Shang-Guan · Yuan-Xiang Lin · De-Zhi Kang · Pei-Sen Yao

Brain sciences · 2022 doi:10.3390/brainsci12081012

Paper

complete

Experiment

complete

Data

partial

Analysis

complete

Execution

absent

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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title
Elevated Hexose-6-Phosphate Dehydrogenase Regulated by OSMR-AS1/hsa-miR-516b-5p Axis Correlates with Poor Prognosis and Dendritic Cells Infiltration of Glioblastoma.
doi
10.3390/brainsci12081012
pmid
36009075
authors array · 8 items
[0]
Yi-Bin Zhang
[1]
Shu-Fa Zheng
[2]
Lin-Jie Ma
[3]
Peng Lin
[4]
Huang-Cheng Shang-Guan
[5]
Yuan-Xiang Lin
[6]
De-Zhi Kang
[7]
Pei-Sen Yao
journal
Brain sciences
year
2022
abstract
Objective Glioblastoma (GBM), a type of malignant glioma, is the most aggressive type of brain tumor and is associated with high mortality. Hexose-6-phosphate dehydrogenase (H6PD) has been detected in multiple tumors and is involved in tumor initiation and progression. However, the specific role and mechanism of H6PD in GBM remain unclear. Methods We performed pan-cancer analysis of expression and prognosis of H6PD in GBM using the Genotype-Tissue Expression Project (GTEx) and The Cancer Genome Atlas (TCGA). Subsequently, noncoding RNAs regulating H6PD expression were obtained by comprehensive analysis, including gene expression, prognosis, correlation, and immune infiltration. Finally, tumor immune infiltrates related to H6PD and survival were performed. Results Higher expression of H6PD was statistically significantly associated with an unfavorable outcome in GBM. Downregulation of hsa-miR-124-3p and hsa-miR-516b-5p in GBM was detected from GSE90603. Subsequently, OSMR-AS1 was observed in the regulation of H6PD via hsa-miR-516b-5p. Moreover, higher H6PD expression significantly correlated with immune infiltration of dendritic cells, immune checkpoint expression, and biomarkers of dendritic cells. Conclusions The OSMR-AS1/ miR-516b-5p axis was identified as the highest-potential upstream ncRNA-related pathway of H6PD in GBM. Furthermore, the present findings demonstrated that H6PD blockading might possess antitumor roles via regulating dendritic cell infiltration and immune checkpoint expression.
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We also analyzed weighted Pearson correlations and p-values using the R package “weights” (https://CRAN.R-project.org/package=weights); p-values less than 0.05 were considered statistically significant.
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The datasets analyzed in this study are available in the following open access repositories. TGGA: The Cancer Genome Atlas (TCGA) database (https://tcga-data.nci.nih.gov/tcga/ (accessed on 19 April 2022)). GEPIA: http://gepia.cancer-pku.cn/detail.php (accessed on 19 April 2022). ENCORI: http://starbase.sysu.edu.cn (accessed on 19 April 2022). miRNet2.0: www.mirnet.ca/miRNet/home.xhtml (accessed on 19 April 2022). The UCSC Xena database: http://xena.ucsc.edu/ (accessed on 19 April 2022). TIMER: https://cistrome.shinyapps.io/timer/ (accessed on 19 April 2022).
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The datasets analyzed in this study are available in the following open access repositories. TGGA: The Cancer Genome Atlas (TCGA) database (https://tcga-data.nci.nih.gov/tcga/ (accessed on 19 April 2022)). GEPIA: http://gepia.cancer-pku.cn/detail.php (accessed on 19 April 2022). ENCORI: http://starbase.sysu.edu.cn (accessed on 19 April 2022). miRNet2.0: www.mirnet.ca/miRNet/home.xhtml (accessed on 19 April 2022). The UCSC Xena database: http://xena.ucsc.edu/ (accessed on 19 April 2022). TIMER: https://cistrome.shinyapps.io/timer/ (accessed on 19 April 2022).
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The datasets analyzed in this study are available in the following open access repositories. TGGA: The Cancer Genome Atlas (TCGA) database (https://tcga-data.nci.nih.gov/tcga/ (accessed on 19 April 2022)). GEPIA: http://gepia.cancer-pku.cn/detail.php (accessed on 19 April 2022). ENCORI: http://starbase.sysu.edu.cn (accessed on 19 April 2022). miRNet2.0: www.mirnet.ca/miRNet/home.xhtml (accessed on 19 April 2022). The UCSC Xena database: http://xena.ucsc.edu/ (accessed on 19 April 2022). TIMER: https://cistrome.shinyapps.io/timer/ (accessed on 19 April 2022).
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miRNA Expression data from Glioblastoma Multiforme patient tumor samples, healthy brain tissue (partly from GBM patients) and NHA cell line and Human fetal astrocyte cell line
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The datasets analyzed in this study are available in the following open access repositories. TGGA: The Cancer Genome Atlas (TCGA) database (https://tcga-data.nci.nih.gov/tcga/ (accessed on 19 April 2022)). GEPIA: http://gepia.cancer-pku.cn/detail.php (accessed on 19 April 2022). ENCORI: http://starbase.sysu.edu.cn (accessed on 19 April 2022). miRNet2.0: www.mirnet.ca/miRNet/home.xhtml (accessed on 19 April 2022). The UCSC Xena database: http://xena.ucsc.edu/ (accessed on 19 April 2022). TIMER: https://cistrome.shinyapps.io/timer/ (accessed on 19 April 2022).
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Hexose-6-phosphate dehydrogenase (H6PD) has been detected in multiple tumors and is involved in tumor initiation and progression. However, the specific role and mechanism of H6PD in GBM remain unclear. Methods We performed pan-cancer analysis of expression and prognosis of H6PD in GBM using the Genotype-Tissue Expression Project (GTEx) and The Cancer Genome Atlas (TCGA). Subsequently, noncoding RNAs regulating H6PD expression were obtained by comprehensive analysis, including gene expression, prognosis, correlation, and immune infiltration. Finally, tumor immune infiltrates related to H6PD and survival were performed. Results Higher expression of H6PD was statistically significantly associated with an unfavorable outcome in GBM. Downregulation of hsa-miR-124-3p and hsa-miR-516b-5p in GBM was detected from GSE90603. Subsequently, OSMR-AS1 was observed in the regulation of H6PD via hsa-miR-516b-5p. Moreover, higher H6PD expression significantly correlated with immune infiltration of dendritic cells, immune checkpoint expression, and biomarkers of dendritic cells. Conclusions The OSMR-AS1/ miR-516b-5p axis was identified as the highest-potential upstream ncRNA-related pathway of H6PD in GBM. Furthermore, the present findings demonstrated that H6PD blockading might possess antitumor roles via regulating dendritic cell infiltration and immune checkpoint expression.", "claims": [{"id": "claim-method", "statement": "We also analyzed weighted Pearson correlations and p-values using the R package “weights” (https://CRAN.R-project.org/package=weights); p-values less than 0.05 were considered statistically significant.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:36009075", "locator": "sections[3] \"2.1. 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