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pmid:36915125

Lipid metabolism-related miRNAs with potential diagnostic roles in prostate cancer.

Tianyuan Zhai · Meng Dou · Yubo Ma · Hong Wang · Fang Liu · Liandong Zhang · Tie Chong · Ziming Wang · Li Xue

Lipids in health and disease · 2023 doi:10.1186/s12944-023-01804-4

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title
Lipid metabolism-related miRNAs with potential diagnostic roles in prostate cancer.
doi
10.1186/s12944-023-01804-4
pmid
36915125
authors array · 9 items
[0]
Tianyuan Zhai
[1]
Meng Dou
[2]
Yubo Ma
[3]
Hong Wang
[4]
Fang Liu
[5]
Liandong Zhang
[6]
Tie Chong
[7]
Ziming Wang
[8]
Li Xue
journal
Lipids in health and disease
year
2023
abstract
BACKGROUND: Prostate cancer (PCa), the second most prevalent solid tumor among men worldwide, has caused greatly increasing mortality in PCa patients. The effects of lipid metabolism on tumor growth have been explored, but the mechanistic details of the association of lipid metabolism disorders with PCa remain largely elusive. METHODS: The RNA sequencing data of the GSE45604 and The Cancer Genome Atlas-Prostate Adenocarcinoma (TCGA-PRAD) datasets were extracted from the Gene Expression Omnibus (GEO) and UCSC Xena databases, respectively. The Molecular Signatures Database (MSigDB) was utilized to identify lipid metabolism-related genes. The limma R package was used to identify differentially expressed lipid metabolism-related genes (DE-LMRGs) and differentially expressed microRNAs (DEMs). Moreover, least absolute shrinkage and selection operator (LASSO), extreme gradient boosting (XGBoost), and support vector machine-recursive feature elimination (SVM-RFE) were applied to select signature miRNAs and construct a lipid metabolism-related diagnostic model. The expression levels of selected differentially expressed lipid metabolism-related miRNAs (DE-LMRMs) in PCa and benign prostate hyperplasia (BPH) specimens were verified using quantitative real-time polymerase chain reaction (qRT‒PCR). Furthermore, a transcription factor (TF)-miRNA‒mRNA network was constructed. Eventually, Kaplan‒Meier (KM) curves were plotted to illustrate the associations between signature miRNA-related mRNAs and TFs and overall survival (OS) along with biochemical recurrence-free survival (BCR). RESULTS: Forty-seven LMRMs were screened based on the correlation analysis of 29 DE-LMRGs and 56 DEMs, in which 27 LMRMs were stably expressed in the GSE45604 dataset. Subsequently, receiver operating characteristic (ROC) curves and machine learning methods were employed to develop a lipid metabolism-related diagnostic signature, which may be of diagnostic value for PCa patients. qRT‒PCR results showed that all seven key DE-LMRMs were differentially expressed between PCa and BPH tissues. Eventually, a TF-miRNA‒mRNA network was constructed. CONCLUSIONS: These results suggested that 7 key diagnostic miRNAs were closely related to PCa pathological processes and provided new targets for the diagnosis and treatment of PCa. Moreover, CLIC6 and SCNN1A linked to miR-200c-3p had good prognostic potential and provided valuable insights into the pathogenesis of PCa.
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To identify LMRMs, DEMs between 52 normal and 499 PCa samples of the TCGA-PRAD dataset were first screened using the limma R package, considering |log2FC|> 1 and P < 0.05 as the screening criteria [20]. Next, DE-LMRMs were identified by performing Pearson's correlation analysis between DEMs and DE-LMRGs, and correlation < -0.3 and P < 0.05 were considered screening criteria.
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sections[7] "Identification of DE-lipid metabolism-related miRNAs (DE-LMRMs)" paragraph 2
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To identify LMRMs, DEMs between 52 normal and 499 PCa samples of the TCGA-PRAD dataset were first screened using the limma R package, considering |log2FC|> 1 and P < 0.05 as the screening criteria [20]. Next, DE-LMRMs were identified by performing Pearson's correlation analysis between DEMs and DE-LMRGs, and correlation < -0.3 and P < 0.05 were considered screening criteria.
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The raw data used in this study were extracted from the GEO database (https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE45604) and TCGA-PRAD database (https://portal.gdc.cancer.gov).
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The raw data used in this study were extracted from the GEO database (https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE45604) and TCGA-PRAD database (https://portal.gdc.cancer.gov).
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To validate the diagnostic signature's predictive ability, ROC curves based on the 7 key diagnostic miRNAs were plotted for the training set and validation set, suggesting that the AUCs were 0.99 and 1, respectively (Fig. 3H and I).
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sections[13] "Identification and validation of key diagnostic miRNAs in PCa" paragraph 2
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To validate the diagnostic signature's predictive ability, ROC curves based on the 7 key diagnostic miRNAs were plotted for the training set and validation set, suggesting that the AUCs were 0.99 and 1, respectively (Fig. 3H and I).
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To validate the diagnostic signature's predictive ability, ROC curves based on the 7 key diagnostic miRNAs were plotted for the training set and validation set, suggesting that the AUCs were 0.99 and 1, respectively (Fig. 3H and I).
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Identification of miRNAs specific for prostate cancer (PCa)
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To identify LMRMs, DEMs between 52 normal and 499 PCa samples of the TCGA-PRAD dataset were first screened using the limma R package, considering |log2FC|> 1 and P < 0.05 as the screening criteria [20]. Next, DE-LMRMs were identified by performing Pearson's correlation analysis between DEMs and DE-LMRGs, and correlation < -0.3 and P < 0.05 were considered screening criteria.
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ith PCa remain largely elusive. METHODS: The RNA sequencing data of the GSE45604 and The Cancer Genome A
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To identify LMRMs, DEMs between 52 normal and 499 PCa samples of the TCGA-PRAD dataset were first screened using the limma R package, considering |log2FC|> 1 and P < 0.05 as the screening criteria [20]. Next, DE-LMRMs were identified by performing Pearson's correlation analysis between DEMs and DE-LMRGs, and correlation < -0.3 and P < 0.05 were considered screening criteria.
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{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:36915125", "kind": "science-record", "revision": 4, "content_hash": "sha256:755e65133867117f42468a4b63f27f67f67bf3306b84e2fbf2d513932d61ea9a", "created_at": "2026-11-01T19:01:33Z", "updated_at": "2026-11-01T22:51:29Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Lipid metabolism-related miRNAs with potential diagnostic roles in prostate cancer.", "doi": "10.1186/s12944-023-01804-4", "pmid": "36915125", "authors": ["Tianyuan Zhai", "Meng Dou", "Yubo Ma", "Hong Wang", "Fang Liu", "Liandong Zhang", "Tie Chong", "Ziming Wang", "Li Xue"], "journal": "Lipids in health and disease", "year": 2023, "abstract": "BACKGROUND: Prostate cancer (PCa), the second most prevalent solid tumor among men worldwide, has caused greatly increasing mortality in PCa patients. The effects of lipid metabolism on tumor growth have been explored, but the mechanistic details of the association of lipid metabolism disorders with PCa remain largely elusive.\nMETHODS: The RNA sequencing data of the GSE45604 and The Cancer Genome Atlas-Prostate Adenocarcinoma (TCGA-PRAD) datasets were extracted from the Gene Expression Omnibus (GEO) and UCSC Xena databases, respectively. The Molecular Signatures Database (MSigDB) was utilized to identify lipid metabolism-related genes. The limma R package was used to identify differentially expressed lipid metabolism-related genes (DE-LMRGs) and differentially expressed microRNAs (DEMs). Moreover, least absolute shrinkage and selection operator (LASSO), extreme gradient boosting (XGBoost), and support vector machine-recursive feature elimination (SVM-RFE) were applied to select signature miRNAs and construct a lipid metabolism-related diagnostic model. The expression levels of selected differentially expressed lipid metabolism-related miRNAs (DE-LMRMs) in PCa and benign prostate hyperplasia (BPH) specimens were verified using quantitative real-time polymerase chain reaction (qRT‒PCR). Furthermore, a transcription factor (TF)-miRNA‒mRNA network was constructed. Eventually, Kaplan‒Meier (KM) curves were plotted to illustrate the associations between signature miRNA-related mRNAs and TFs and overall survival (OS) along with biochemical recurrence-free survival (BCR).\nRESULTS: Forty-seven LMRMs were screened based on the correlation analysis of 29 DE-LMRGs and 56 DEMs, in which 27 LMRMs were stably expressed in the GSE45604 dataset. Subsequently, receiver operating characteristic (ROC) curves and machine learning methods were employed to develop a lipid metabolism-related diagnostic signature, which may be of diagnostic value for PCa patients. qRT‒PCR results showed that all seven key DE-LMRMs were differentially expressed between PCa and BPH tissues. Eventually, a TF-miRNA‒mRNA network was constructed.\nCONCLUSIONS: These results suggested that 7 key diagnostic miRNAs were closely related to PCa pathological processes and provided new targets for the diagnosis and treatment of PCa. Moreover, CLIC6 and SCNN1A linked to miR-200c-3p had good prognostic potential and provided valuable insights into the pathogenesis of PCa.", "claims": [{"id": "claim-method", "statement": "To identify LMRMs, DEMs between 52 normal and 499 PCa samples of the TCGA-PRAD dataset were first screened using the limma R package, considering |log2FC|> 1 and P < 0.05 as the screening criteria [20]. 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