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pmid:34827123

The Identification of RNA Modification Gene PUS7 as a Potential Biomarker of Ovarian Cancer.

Huimin Li · Lin Chen · Yunsong Han · Fangfang Zhang · Yanyan Wang · Yali Han · Yange Wang · Qiang Wang · Xiangqian Guo

Biology · 2021 doi:10.3390/biology10111130

Paper

complete

Experiment

complete

Data

partial

Analysis

partial

Execution

absent

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title
The Identification of RNA Modification Gene PUS7 as a Potential Biomarker of Ovarian Cancer.
doi
10.3390/biology10111130
pmid
34827123
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[0]
Huimin Li
[1]
Lin Chen
[2]
Yunsong Han
[3]
Fangfang Zhang
[4]
Yanyan Wang
[5]
Yali Han
[6]
Yange Wang
[7]
Qiang Wang
[8]
Xiangqian Guo
journal
Biology
year
2021
abstract
RNA modifications are reversible, dynamically regulated, and involved in a variety of diseases such as cancers. Given the lack of efficient and reliable biomarkers for early diagnosis of ovarian cancer (OV), this study was designed to explore the role of RNA modification genes (RMGs) in the diagnosis of OV. Herein, 132 RMGs were retrieved in PubMed, 638 OV and 18 normal ovary samples were retrieved in The Cancer Genome Atlas (TCGA), and GSE18520 cohorts were collected for differential analysis. Finally, PUS7 (Pseudouridine Synthase 7) as differentially expressed RMGs (DEGs-RMGs) was identified as a diagnostic biomarker candidate and evaluated for its specificity and sensitivity using Receiver Operating Characteristic (ROC) analysis in TCGA and GEO data. The protein expression, mutation, protein interaction networks, correlated genes, related pathways, biological processes, cell components, and molecular functions of PUS7 were analyzed as well. The upregulation of PUS7 protein in OV was confirmed by the staining images in HPA and tissue arrays. Collectively, the findings of the present study point towards the potential of PUS7 as a diagnostic marker and therapeutic target for ovarian cancer.
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The ROC curve was constructed using PUS7 expression profiles in the OV and normal samples by GraphPad Prism 8.0.
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The ROC curve was constructed using PUS7 expression profiles in the OV and normal samples by GraphPad Prism 8.0.
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To validate the overexpression of PUS7 in OV rather than normal samples, an Oncomine analysis was performed on ovarian cancer with different pathological types, and found that the PUS7 expression is highly elevated in OV samples with fold change >1 and p < 0.05 (as presented in Figure 3A,B and Table 1).
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To validate the overexpression of PUS7 in OV rather than normal samples, an Oncomine analysis was performed on ovarian cancer with different pathological types, and found that the PUS7 expression is highly elevated in OV samples with fold change >1 and p < 0.05 (as presented in Figure 3A,B and Table 1).
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sections[14] "3.2. Expression Validation and Mutation Analysis for PUS7 in Ovarian Cancer" paragraph 2
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To validate the overexpression of PUS7 in OV rather than normal samples, an Oncomine analysis was performed on ovarian cancer with different pathological types, and found that the PUS7 expression is highly elevated in OV samples with fold change >1 and p < 0.05 (as presented in Figure 3A,B and Table 1).
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To validate the overexpression of PUS7 in OV rather than normal samples, an Oncomine analysis was performed on ovarian cancer with different pathological types, and found that the PUS7 expression is highly elevated in OV samples with fold change >1 and p < 0.05 (as presented in Figure 3A,B and Table 1).
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Given the lack of efficient and reliable biomarkers for early diagnosis of ovarian cancer (OV), this study was designed to explore the role of RNA modification genes (RMGs) in the diagnosis of OV. Herein, 132 RMGs were retrieved in PubMed, 638 OV and 18 normal ovary samples were retrieved in The Cancer Genome Atlas (TCGA), and GSE18520 cohorts were collected for differential analysis. Finally, PUS7 (Pseudouridine Synthase 7) as differentially expressed RMGs (DEGs-RMGs) was identified as a diagnostic biomarker candidate and evaluated for its specificity and sensitivity using Receiver Operating Characteristic (ROC) analysis in TCGA and GEO data. The protein expression, mutation, protein interaction networks, correlated genes, related pathways, biological processes, cell components, and molecular functions of PUS7 were analyzed as well. The upregulation of PUS7 protein in OV was confirmed by the staining images in HPA and tissue arrays. 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