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POLRMT over‐expression is linked to WNT/beta‐catenin signaling, immune infiltration, and unfavorable outcomes in lung adenocarcinoma patients
BACKGROUND: Mitochondrial RNA polymerase (POLRMT) is essential for the expression of mitochondrial genes. In recent studies, POLRMT expression promoted non‐small cell cancer cell proliferation in cell lines and xenografts. The present study investigated the impact of POLRMT expression and function o...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10417304/ https://www.ncbi.nlm.nih.gov/pubmed/37283308 http://dx.doi.org/10.1002/cam4.6174 |
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author | Huang, Yongkang Qian, Yajuan Xing, Yufei Pei, Yongjian Zhang, Beilei Li, Ting Pan, Xue Zhong, Anyuan Du, Juan Zhou, Tong Shi, Minhua |
author_facet | Huang, Yongkang Qian, Yajuan Xing, Yufei Pei, Yongjian Zhang, Beilei Li, Ting Pan, Xue Zhong, Anyuan Du, Juan Zhou, Tong Shi, Minhua |
author_sort | Huang, Yongkang |
collection | PubMed |
description | BACKGROUND: Mitochondrial RNA polymerase (POLRMT) is essential for the expression of mitochondrial genes. In recent studies, POLRMT expression promoted non‐small cell cancer cell proliferation in cell lines and xenografts. The present study investigated the impact of POLRMT expression and function on lung adenocarcinoma (LUAD) patients. METHOD: Multi‐omics data (genomics, transcriptomics, and proteomics) from publicly available databases were used to assess the role of POLRMT expression and function in LUAD. These findings were further verified using cancer tissues from clinical samples. RESULTS: POLRMT was over‐expressed in LUADs, with mutation frequencies ranging from 1.30% to 5.71%. Over‐expression of POLRMT was associated with an abnormal clinicopathological condition resulting in a decreased lifespan. Furthermore, gene sets enrich analysis revealed that POLRMT expression was linked to WNT/beta‐catenin signaling; the expression of downstream target genes was positively correlated with POLRMT expression. Also, POLRMT expression was positively correlated with immunosuppressive genes, thereby affecting immune infiltration. CONCLUSION: POLRMT is over‐expressed in LUAD, thereby impacting patient survival. It is also involved in WNT/beta‐catenin signaling and may affect tumor infiltration. |
format | Online Article Text |
id | pubmed-10417304 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-104173042023-08-12 POLRMT over‐expression is linked to WNT/beta‐catenin signaling, immune infiltration, and unfavorable outcomes in lung adenocarcinoma patients Huang, Yongkang Qian, Yajuan Xing, Yufei Pei, Yongjian Zhang, Beilei Li, Ting Pan, Xue Zhong, Anyuan Du, Juan Zhou, Tong Shi, Minhua Cancer Med Research Articles BACKGROUND: Mitochondrial RNA polymerase (POLRMT) is essential for the expression of mitochondrial genes. In recent studies, POLRMT expression promoted non‐small cell cancer cell proliferation in cell lines and xenografts. The present study investigated the impact of POLRMT expression and function on lung adenocarcinoma (LUAD) patients. METHOD: Multi‐omics data (genomics, transcriptomics, and proteomics) from publicly available databases were used to assess the role of POLRMT expression and function in LUAD. These findings were further verified using cancer tissues from clinical samples. RESULTS: POLRMT was over‐expressed in LUADs, with mutation frequencies ranging from 1.30% to 5.71%. Over‐expression of POLRMT was associated with an abnormal clinicopathological condition resulting in a decreased lifespan. Furthermore, gene sets enrich analysis revealed that POLRMT expression was linked to WNT/beta‐catenin signaling; the expression of downstream target genes was positively correlated with POLRMT expression. Also, POLRMT expression was positively correlated with immunosuppressive genes, thereby affecting immune infiltration. CONCLUSION: POLRMT is over‐expressed in LUAD, thereby impacting patient survival. It is also involved in WNT/beta‐catenin signaling and may affect tumor infiltration. John Wiley and Sons Inc. 2023-06-07 /pmc/articles/PMC10417304/ /pubmed/37283308 http://dx.doi.org/10.1002/cam4.6174 Text en © 2023 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Huang, Yongkang Qian, Yajuan Xing, Yufei Pei, Yongjian Zhang, Beilei Li, Ting Pan, Xue Zhong, Anyuan Du, Juan Zhou, Tong Shi, Minhua POLRMT over‐expression is linked to WNT/beta‐catenin signaling, immune infiltration, and unfavorable outcomes in lung adenocarcinoma patients |
title |
POLRMT over‐expression is linked to WNT/beta‐catenin signaling, immune infiltration, and unfavorable outcomes in lung adenocarcinoma patients |
title_full |
POLRMT over‐expression is linked to WNT/beta‐catenin signaling, immune infiltration, and unfavorable outcomes in lung adenocarcinoma patients |
title_fullStr |
POLRMT over‐expression is linked to WNT/beta‐catenin signaling, immune infiltration, and unfavorable outcomes in lung adenocarcinoma patients |
title_full_unstemmed |
POLRMT over‐expression is linked to WNT/beta‐catenin signaling, immune infiltration, and unfavorable outcomes in lung adenocarcinoma patients |
title_short |
POLRMT over‐expression is linked to WNT/beta‐catenin signaling, immune infiltration, and unfavorable outcomes in lung adenocarcinoma patients |
title_sort | polrmt over‐expression is linked to wnt/beta‐catenin signaling, immune infiltration, and unfavorable outcomes in lung adenocarcinoma patients |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10417304/ https://www.ncbi.nlm.nih.gov/pubmed/37283308 http://dx.doi.org/10.1002/cam4.6174 |
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