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The novel putative methyltransferase METTL7A as one prognostic biomarker potentially associated with immune infiltration in human renal cancer

Authors :
Zhiqian Yang
Wei Zhang
Lintai Li
Nan Hu
Xiangnan Dong
Yumei Chen
Wanxia Cai
Lianghong Yin
Fanna Liu
Donge Tang
Yong Dai
Source :
Heliyon, Vol 9, Iss 4, Pp e15371- (2023)
Publication Year :
2023
Publisher :
Elsevier, 2023.

Abstract

Among urological cancers, renal cancer has the highest fatality rate. In a previous pan-cancer study of the METTL family, we observed a stronger association between the METTL family members and the risk of renal cancer compared to other cancers. Among these members, METTL7A, a potential methyltransferase, was identified as a protective factor, although its role and mechanism in renal cancer remain unclear. In this study, we utilized public databases to examine the expression of METTL7A in renal cancer tissues and normal tissues and found that METTL7A expression was much lower in renal cancer tissues. We also noticed a link between low METTL7A expression and poor prognosis for patients. According to the results of our functional enrichment analysis, METTL7A may have a role in immunological functions in renal cancer. METTL7A expression was strongly linked with the degrees of immune cell infiltration and expression of numerous immunological components. METTL7A had significantly different effects on the survival times of renal cancer patients with high or low immune infiltration. Our findings suggest that METTL7A may be used as both a prognostic biomarker and an immunological target for kidney cancer. In conclusion, our study sheds light on the importance of METTL7A in renal cancer and emphasizes the potential of targeting METTL7A as a novel therapeutic strategy for kidney cancer.

Details

Language :
English
ISSN :
24058440
Volume :
9
Issue :
4
Database :
Directory of Open Access Journals
Journal :
Heliyon
Publication Type :
Academic Journal
Accession number :
edsdoj.59a69fc9a8a74d7c8417202d0ff7b07d
Document Type :
article
Full Text :
https://doi.org/10.1016/j.heliyon.2023.e15371