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The novel putative methyltransferase METTL7A as one prognostic biomarker potentially associated with immune infiltration in human renal cancer
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 methyltransf...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10133759/ https://www.ncbi.nlm.nih.gov/pubmed/37123902 http://dx.doi.org/10.1016/j.heliyon.2023.e15371 |
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author | Yang, Zhiqian Zhang, Wei Li, Lintai Hu, Nan Dong, Xiangnan Chen, Yumei Cai, Wanxia Yin, Lianghong Liu, Fanna Tang, Donge Dai, Yong |
author_facet | Yang, Zhiqian Zhang, Wei Li, Lintai Hu, Nan Dong, Xiangnan Chen, Yumei Cai, Wanxia Yin, Lianghong Liu, Fanna Tang, Donge Dai, Yong |
author_sort | Yang, Zhiqian |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-10133759 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-101337592023-04-28 The novel putative methyltransferase METTL7A as one prognostic biomarker potentially associated with immune infiltration in human renal cancer Yang, Zhiqian Zhang, Wei Li, Lintai Hu, Nan Dong, Xiangnan Chen, Yumei Cai, Wanxia Yin, Lianghong Liu, Fanna Tang, Donge Dai, Yong Heliyon Research Article 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. Elsevier 2023-04-11 /pmc/articles/PMC10133759/ /pubmed/37123902 http://dx.doi.org/10.1016/j.heliyon.2023.e15371 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Article Yang, Zhiqian Zhang, Wei Li, Lintai Hu, Nan Dong, Xiangnan Chen, Yumei Cai, Wanxia Yin, Lianghong Liu, Fanna Tang, Donge Dai, Yong The novel putative methyltransferase METTL7A as one prognostic biomarker potentially associated with immune infiltration in human renal cancer |
title | The novel putative methyltransferase METTL7A as one prognostic biomarker potentially associated with immune infiltration in human renal cancer |
title_full | The novel putative methyltransferase METTL7A as one prognostic biomarker potentially associated with immune infiltration in human renal cancer |
title_fullStr | The novel putative methyltransferase METTL7A as one prognostic biomarker potentially associated with immune infiltration in human renal cancer |
title_full_unstemmed | The novel putative methyltransferase METTL7A as one prognostic biomarker potentially associated with immune infiltration in human renal cancer |
title_short | The novel putative methyltransferase METTL7A as one prognostic biomarker potentially associated with immune infiltration in human renal cancer |
title_sort | novel putative methyltransferase mettl7a as one prognostic biomarker potentially associated with immune infiltration in human renal cancer |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10133759/ https://www.ncbi.nlm.nih.gov/pubmed/37123902 http://dx.doi.org/10.1016/j.heliyon.2023.e15371 |
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