CENPE and LDHA were potential prognostic biomarkers of chromophobe renal cell carcinoma

Abstract Background Most sarcomatoid differentiated renal cell carcinoma was differentiated from Chromophobe renal cell carcinoma (KICH) and related to a bad prognosis. Thus, finding biomarkers is important for the therapy of KICH. Methods The UCSC was used for determining the expression of mRNA and...

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Main Authors: Hui-feng Wu, Hao Liu, Zhe-wei Zhang, Ji-min Chen
Format: Article
Language:English
Published: BMC 2023-11-01
Series:European Journal of Medical Research
Subjects:
Online Access:https://doi.org/10.1186/s40001-023-01449-0
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author Hui-feng Wu
Hao Liu
Zhe-wei Zhang
Ji-min Chen
author_facet Hui-feng Wu
Hao Liu
Zhe-wei Zhang
Ji-min Chen
author_sort Hui-feng Wu
collection DOAJ
description Abstract Background Most sarcomatoid differentiated renal cell carcinoma was differentiated from Chromophobe renal cell carcinoma (KICH) and related to a bad prognosis. Thus, finding biomarkers is important for the therapy of KICH. Methods The UCSC was used for determining the expression of mRNA and miRNA and clinical data in KICH and normal samples. KEGG and GO were used for predicting potential function of differently expressed genes (DEGs). Optimal prognostic markers were determined by Lasso regression. Kaplan–Meier survival, ROC, and cox regression were used for assessing prognosis value. GSEA was used for predicting potential function of markers. The relations between markers and immune cell infiltration were determined by Pearson method. The upstream miRNA of markers was predicted in TargetScan and DIANA. Results The 6162 upregulated and 13,903 downregulated DEGs were identified in KICH. Further CENPE and LDHA were screened out as optimal prognostic risk signatures. CENPE was highly expressed while LDHA was lowly expressed in KICH samples, and the high expressions of 2 genes contributed to bad prognosis. The functions of CENPE and LDHA were mainly enriched in proliferation related pathways such as cell cycle and DNA replication. In addition, the correlation of 2 genes with immune infiltrates in KICH was also observed. Finally, we found that has-miR-577 was the common upstream of 2 genes and the binding sites can be predicted. Conclusion CENPE and LDHA were identified as the important prognostic biomarkers in KICH, and they might be involved in the proliferation of cancer cell.
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spelling doaj.art-c418e502a04b464c8ce013efe57291052023-11-05T12:11:13ZengBMCEuropean Journal of Medical Research2047-783X2023-11-0128111310.1186/s40001-023-01449-0CENPE and LDHA were potential prognostic biomarkers of chromophobe renal cell carcinomaHui-feng Wu0Hao Liu1Zhe-wei Zhang2Ji-min Chen3Department of Urology, The Second Affiliated Hospital, Zhejiang University School of MedicineDepartment of Urology, The Second Affiliated Hospital, Zhejiang University School of MedicineDepartment of Urology, The Second Affiliated Hospital, Zhejiang University School of MedicineDepartment of Urology, The Second Affiliated Hospital, Zhejiang University School of MedicineAbstract Background Most sarcomatoid differentiated renal cell carcinoma was differentiated from Chromophobe renal cell carcinoma (KICH) and related to a bad prognosis. Thus, finding biomarkers is important for the therapy of KICH. Methods The UCSC was used for determining the expression of mRNA and miRNA and clinical data in KICH and normal samples. KEGG and GO were used for predicting potential function of differently expressed genes (DEGs). Optimal prognostic markers were determined by Lasso regression. Kaplan–Meier survival, ROC, and cox regression were used for assessing prognosis value. GSEA was used for predicting potential function of markers. The relations between markers and immune cell infiltration were determined by Pearson method. The upstream miRNA of markers was predicted in TargetScan and DIANA. Results The 6162 upregulated and 13,903 downregulated DEGs were identified in KICH. Further CENPE and LDHA were screened out as optimal prognostic risk signatures. CENPE was highly expressed while LDHA was lowly expressed in KICH samples, and the high expressions of 2 genes contributed to bad prognosis. The functions of CENPE and LDHA were mainly enriched in proliferation related pathways such as cell cycle and DNA replication. In addition, the correlation of 2 genes with immune infiltrates in KICH was also observed. Finally, we found that has-miR-577 was the common upstream of 2 genes and the binding sites can be predicted. Conclusion CENPE and LDHA were identified as the important prognostic biomarkers in KICH, and they might be involved in the proliferation of cancer cell.https://doi.org/10.1186/s40001-023-01449-0CENPELDHAChromophobe renal cell carcinomaPrognosis
spellingShingle Hui-feng Wu
Hao Liu
Zhe-wei Zhang
Ji-min Chen
CENPE and LDHA were potential prognostic biomarkers of chromophobe renal cell carcinoma
European Journal of Medical Research
CENPE
LDHA
Chromophobe renal cell carcinoma
Prognosis
title CENPE and LDHA were potential prognostic biomarkers of chromophobe renal cell carcinoma
title_full CENPE and LDHA were potential prognostic biomarkers of chromophobe renal cell carcinoma
title_fullStr CENPE and LDHA were potential prognostic biomarkers of chromophobe renal cell carcinoma
title_full_unstemmed CENPE and LDHA were potential prognostic biomarkers of chromophobe renal cell carcinoma
title_short CENPE and LDHA were potential prognostic biomarkers of chromophobe renal cell carcinoma
title_sort cenpe and ldha were potential prognostic biomarkers of chromophobe renal cell carcinoma
topic CENPE
LDHA
Chromophobe renal cell carcinoma
Prognosis
url https://doi.org/10.1186/s40001-023-01449-0
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AT haoliu cenpeandldhawerepotentialprognosticbiomarkersofchromophoberenalcellcarcinoma
AT zheweizhang cenpeandldhawerepotentialprognosticbiomarkersofchromophoberenalcellcarcinoma
AT jiminchen cenpeandldhawerepotentialprognosticbiomarkersofchromophoberenalcellcarcinoma