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pmid:35227296

Identification of key genes associated with polycystic ovary syndrome (PCOS) and ovarian cancer using an integrated bioinformatics analysis.

Juan Zou · Yukun Li · Nianchun Liao · Jue Liu · Qunfeng Zhang · Min Luo · Jiao Xiao · Yanhua Chen · Mengjie Wang · Kexin Chen · Juan Zeng · Zhongcheng Mo

Journal of ovarian research · 2022 doi:10.1186/s13048-022-00962-w

Paper

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Experiment

partial

Data

partial

Analysis

partial

Execution

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title
Identification of key genes associated with polycystic ovary syndrome (PCOS) and ovarian cancer using an integrated bioinformatics analysis.
doi
10.1186/s13048-022-00962-w
pmid
35227296
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[0]
Juan Zou
[1]
Yukun Li
[2]
Nianchun Liao
[3]
Jue Liu
[4]
Qunfeng Zhang
[5]
Min Luo
[6]
Jiao Xiao
[7]
Yanhua Chen
[8]
Mengjie Wang
[9]
Kexin Chen
[10]
Juan Zeng
[11]
Zhongcheng Mo
journal
Journal of ovarian research
year
2022
abstract
BACKGROUND: Accumulating evidence suggests a strong association between polycystic ovary syndrome (PCOS) and ovarian cancer (OC), but the potential molecular mechanism remains unclear. In this study, we identified previously unrecognized genes that are significantly correlated with PCOS and OC via bioinformatics. MATERIALS AND METHODS: Multiple bioinformatic analyses, such as differential expression analysis, univariate Cox analysis, functional and pathway enrichment analysis, protein-protein interaction (PPI) network construction, survival analysis, and immune infiltration analysis, were utilized. We further evaluated the effect of OGN on FSHR expression via immunofluorescence. RESULTS: TCGA-OC, GSE140082 (for OC) and GSE34526 (for PCOS) datasets were downloaded. Twelve genes, including RNF144B, LPAR3, CRISPLD2, JCHAIN, OR7E14P, IL27RA, PTPRD, STAT1, NR4A1, OGN, GALNT6 and CXCL11, were identified as signature genes. Drug sensitivity analysis showed that OGN might represent a hub gene in the progression of PCOS and OC. Experimental analysis found that OGN could increase FSHR expression, indicating that OGN could regulate the hormonal response in PCOS and OC. Furthermore, correlation analysis indicated that OGN function might be closely related to m6A and ferroptosis. CONCLUSIONS: Our study identified a 12-gene signature that might be involved in the prognostic significance of OC. Furthermore, the hub gene OGN represent a significant gene involved in OC and PCOS progression by regulating the hormonal response.
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ted the effect of OGN on FSHR expression via immunofluorescence. RESULTS: TCGA-OC, GSE140082 (for OC) and GS
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Materials and methods Cell culture and transfection Human ovarian cancer cell lines (SKOV3 and K
[1]
Biotechnology, MD, USA). For transient cell transfection, SKOV3 and KGN cells were seeded in 6-well p
[2]
lates for 24 h. After incubation, cells were transfected with 3 μg empty vector and 3 μg OGN overexpr
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Complete file
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In this study, we identified previously unrecognized genes that are significantly correlated with PCOS and OC via bioinformatics.\nMATERIALS AND METHODS: Multiple bioinformatic analyses, such as differential expression analysis, univariate Cox analysis, functional and pathway enrichment analysis, protein-protein interaction (PPI) network construction, survival analysis, and immune infiltration analysis, were utilized. We further evaluated the effect of OGN on FSHR expression via immunofluorescence.\nRESULTS: TCGA-OC, GSE140082 (for OC) and GSE34526 (for PCOS) datasets were downloaded. Twelve genes, including RNF144B, LPAR3, CRISPLD2, JCHAIN, OR7E14P, IL27RA, PTPRD, STAT1, NR4A1, OGN, GALNT6 and CXCL11, were identified as signature genes. Drug sensitivity analysis showed that OGN might represent a hub gene in the progression of PCOS and OC. Experimental analysis found that OGN could increase FSHR expression, indicating that OGN could regulate the hormonal response in PCOS and OC. 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