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Mining database and verification of PIK3CB as a marker predicting prognosis and immune infiltration in renal clear cell carcinoma
BACKGROUND: Kidney renal clear cell carcinoma (KIRC) was the most prevalent malignancy of urinary system. Phosphatidylinositol 3-kinase pathway exerted a vital function in tumor proliferation, invasion, and survival by integrating extracellular growth signals. METHODS: The expression and clinical si...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9276396/ https://www.ncbi.nlm.nih.gov/pubmed/35665729 http://dx.doi.org/10.1097/MD.0000000000029254 |
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author | Ye, Jianzhong Zeng, Tao |
author_facet | Ye, Jianzhong Zeng, Tao |
author_sort | Ye, Jianzhong |
collection | PubMed |
description | BACKGROUND: Kidney renal clear cell carcinoma (KIRC) was the most prevalent malignancy of urinary system. Phosphatidylinositol 3-kinase pathway exerted a vital function in tumor proliferation, invasion, and survival by integrating extracellular growth signals. METHODS: The expression and clinical significance of PIK3CB in KIRC was explored using bioinformatics analysis. And qRT-PCR was performed to verify our results. RESULTS: PIK3CB was downregulated at mRNA and protein level in KIRC. KIRC patients with low PIK3CB expression indicated a worse overall survival, progression free survival, and disease-free survival. A predictive nomogram was constructed and demonstrated that the predicted calibration plots for 1-year, 3-year, and 5-year OS probabilities showed good agreement compared with the actual OS of KIRC patients. Validation research demonstrated a downregulation of PIK3CB in KIRC tissues and a poor overall survival in KIRC patients with low PIK3CB expression. Furthermore, Cox regression analysis revealed that PIK3CB expression was an independent prognostic factor for KIRC. PIK3CB expression showed positive correlation with the abundance of immune cells. Moreover, enrichment analysis revealed that PIK3CB and associated genes were mainly associated with RNA splicing and JAK-STAT signaling pathway. CONCLUSION: Our study suggested that PIK3CB was a potential biomarker for prognosis and correlated with immune infiltrates in KIRC. |
format | Online Article Text |
id | pubmed-9276396 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-92763962022-08-01 Mining database and verification of PIK3CB as a marker predicting prognosis and immune infiltration in renal clear cell carcinoma Ye, Jianzhong Zeng, Tao Medicine (Baltimore) 7300 BACKGROUND: Kidney renal clear cell carcinoma (KIRC) was the most prevalent malignancy of urinary system. Phosphatidylinositol 3-kinase pathway exerted a vital function in tumor proliferation, invasion, and survival by integrating extracellular growth signals. METHODS: The expression and clinical significance of PIK3CB in KIRC was explored using bioinformatics analysis. And qRT-PCR was performed to verify our results. RESULTS: PIK3CB was downregulated at mRNA and protein level in KIRC. KIRC patients with low PIK3CB expression indicated a worse overall survival, progression free survival, and disease-free survival. A predictive nomogram was constructed and demonstrated that the predicted calibration plots for 1-year, 3-year, and 5-year OS probabilities showed good agreement compared with the actual OS of KIRC patients. Validation research demonstrated a downregulation of PIK3CB in KIRC tissues and a poor overall survival in KIRC patients with low PIK3CB expression. Furthermore, Cox regression analysis revealed that PIK3CB expression was an independent prognostic factor for KIRC. PIK3CB expression showed positive correlation with the abundance of immune cells. Moreover, enrichment analysis revealed that PIK3CB and associated genes were mainly associated with RNA splicing and JAK-STAT signaling pathway. CONCLUSION: Our study suggested that PIK3CB was a potential biomarker for prognosis and correlated with immune infiltrates in KIRC. Lippincott Williams & Wilkins 2022-06-03 /pmc/articles/PMC9276396/ /pubmed/35665729 http://dx.doi.org/10.1097/MD.0000000000029254 Text en Copyright © 2022 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) |
spellingShingle | 7300 Ye, Jianzhong Zeng, Tao Mining database and verification of PIK3CB as a marker predicting prognosis and immune infiltration in renal clear cell carcinoma |
title | Mining database and verification of PIK3CB as a marker predicting prognosis and immune infiltration in renal clear cell carcinoma |
title_full | Mining database and verification of PIK3CB as a marker predicting prognosis and immune infiltration in renal clear cell carcinoma |
title_fullStr | Mining database and verification of PIK3CB as a marker predicting prognosis and immune infiltration in renal clear cell carcinoma |
title_full_unstemmed | Mining database and verification of PIK3CB as a marker predicting prognosis and immune infiltration in renal clear cell carcinoma |
title_short | Mining database and verification of PIK3CB as a marker predicting prognosis and immune infiltration in renal clear cell carcinoma |
title_sort | mining database and verification of pik3cb as a marker predicting prognosis and immune infiltration in renal clear cell carcinoma |
topic | 7300 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9276396/ https://www.ncbi.nlm.nih.gov/pubmed/35665729 http://dx.doi.org/10.1097/MD.0000000000029254 |
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