A New Prognostic Risk Signature of Eight Ferroptosis-Related Genes in the Clear Cell Renal Cell Carcinoma

Clear cell renal cell carcinoma (ccRCC) is the most common renal cell carcinoma and has poor prognosis in the locally advanced stage. Ferroptosis, a relatively new type of cell death, has gained significant attention in recent years. This study aimed to explore the prognostic value of ferroptosis-re...

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Published inFrontiers in oncology Vol. 11; p. 700084
Main Authors Chen, Ji, Zhan, Yating, Zhang, Rongrong, Chen, Bo, Huang, Junting, Li, Chunxue, Zhang, Wenjie, Wang, Yajing, Gao, Yuxiang, Zheng, Jianjian, Li, Yeping
Format Journal Article
LanguageEnglish
Published Frontiers Media S.A 25.06.2021
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Summary:Clear cell renal cell carcinoma (ccRCC) is the most common renal cell carcinoma and has poor prognosis in the locally advanced stage. Ferroptosis, a relatively new type of cell death, has gained significant attention in recent years. This study aimed to explore the prognostic value of ferroptosis-related genes (FRGs) in ccRCC. In this study, 50 differentially expressed FRGs between ccRCC and adjacent normal kidney tissues were identified, 26 of them correlated with overall survival (OS) ( P < 0.05). Eight optimal FRGs were selected by Lasso regression and multivariate Cox regression analysis, and used to construct a new prognostic risk signature to predict the prognosis of ccRCC patients. In addition, the signature passed the validation of prognostic survival analyses by a significant margin, and the risk score was identified as an independent prognostic marker via Cox regression analyses. Further studies indicated that the signature was significantly correlated with immune cell infiltration. Moreover, the levels of eight FRGs were examined in ccRCC. Collectively, the 8-FRG prognostic risk signature helps the clinicians predict the prognosis and OS of the patients, and standardize prognostic assessments.
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These authors have contributed equally to this work
Reviewed by: Matteo Manfredi, University of Turin, Italy; Piotr Bryniarski, Medical University of Silesia, Poland
This article was submitted to Genitourinary Oncology, a section of the journal Frontiers in Oncology
Edited by: Daniela Terracciano, University of Naples Federico II, Italy
ISSN:2234-943X
2234-943X
DOI:10.3389/fonc.2021.700084