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TCOF1 coordinates oncogenic activation and rRNA production and promotes tumorigenesis in HCC
Treacle ribosome biogenesis factor 1 (TCOF1) is a nucleolar factor that regulates ribosomal DNA (rDNA) transcription in the nucleolus. TCOF1 has been previously reported to be implicated in Treacher Collins–Franceschetti syndrome (TCS), a congenital disorder of craniofacial development. Except TCS,...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8819287/ https://www.ncbi.nlm.nih.gov/pubmed/34904330 http://dx.doi.org/10.1111/cas.15242 |
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author | Wu, Chaoshen Xia, Dian Wang, Dian Wang, Shu Sun, Zhaoran Xu, Bihuai Zhang, Daoyong |
author_facet | Wu, Chaoshen Xia, Dian Wang, Dian Wang, Shu Sun, Zhaoran Xu, Bihuai Zhang, Daoyong |
author_sort | Wu, Chaoshen |
collection | PubMed |
description | Treacle ribosome biogenesis factor 1 (TCOF1) is a nucleolar factor that regulates ribosomal DNA (rDNA) transcription in the nucleolus. TCOF1 has been previously reported to be implicated in Treacher Collins–Franceschetti syndrome (TCS), a congenital disorder of craniofacial development. Except TCS, TCOF1 has not been reported to be involved in other diseases so far. Here, we show that TCOF1 expression is aberrantly elevated in human hepatocellular carcinoma (HCC) and correlates with HCC progression and poor outcome. In vitro and in vivo studies reveal oncogenic roles of TCOF1 in HCC. Mechanistically, TCOF1 regulates KRAS‐activated genes and epithelial‐mesenchymal transition (EMT) genes in HCC and is required for the increased ribosomal RNA (rRNA) production, a hallmark of cancer. Interestingly, our analysis reveals an inverse correlation between TCOF1 expression and tumor infiltration of antitumor immune cells, suggesting that TCOF1 may also have an important impact on antitumor immune responses in HCC. Together, our findings support a model in which TCOF1 coordinates oncogenic activation and rRNA production to promote HCC tumorigenesis. The inverse correlation between TCOF1 expression and the infiltration of antitumor immune cells opens a new avenue to understanding the promoting role of TCOF in HCC tumorigenesis. |
format | Online Article Text |
id | pubmed-8819287 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-88192872022-02-09 TCOF1 coordinates oncogenic activation and rRNA production and promotes tumorigenesis in HCC Wu, Chaoshen Xia, Dian Wang, Dian Wang, Shu Sun, Zhaoran Xu, Bihuai Zhang, Daoyong Cancer Sci Original Articles Treacle ribosome biogenesis factor 1 (TCOF1) is a nucleolar factor that regulates ribosomal DNA (rDNA) transcription in the nucleolus. TCOF1 has been previously reported to be implicated in Treacher Collins–Franceschetti syndrome (TCS), a congenital disorder of craniofacial development. Except TCS, TCOF1 has not been reported to be involved in other diseases so far. Here, we show that TCOF1 expression is aberrantly elevated in human hepatocellular carcinoma (HCC) and correlates with HCC progression and poor outcome. In vitro and in vivo studies reveal oncogenic roles of TCOF1 in HCC. Mechanistically, TCOF1 regulates KRAS‐activated genes and epithelial‐mesenchymal transition (EMT) genes in HCC and is required for the increased ribosomal RNA (rRNA) production, a hallmark of cancer. Interestingly, our analysis reveals an inverse correlation between TCOF1 expression and tumor infiltration of antitumor immune cells, suggesting that TCOF1 may also have an important impact on antitumor immune responses in HCC. Together, our findings support a model in which TCOF1 coordinates oncogenic activation and rRNA production to promote HCC tumorigenesis. The inverse correlation between TCOF1 expression and the infiltration of antitumor immune cells opens a new avenue to understanding the promoting role of TCOF in HCC tumorigenesis. John Wiley and Sons Inc. 2021-12-29 2022-02 /pmc/articles/PMC8819287/ /pubmed/34904330 http://dx.doi.org/10.1111/cas.15242 Text en © 2021 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Wu, Chaoshen Xia, Dian Wang, Dian Wang, Shu Sun, Zhaoran Xu, Bihuai Zhang, Daoyong TCOF1 coordinates oncogenic activation and rRNA production and promotes tumorigenesis in HCC |
title | TCOF1 coordinates oncogenic activation and rRNA production and promotes tumorigenesis in HCC |
title_full | TCOF1 coordinates oncogenic activation and rRNA production and promotes tumorigenesis in HCC |
title_fullStr | TCOF1 coordinates oncogenic activation and rRNA production and promotes tumorigenesis in HCC |
title_full_unstemmed | TCOF1 coordinates oncogenic activation and rRNA production and promotes tumorigenesis in HCC |
title_short | TCOF1 coordinates oncogenic activation and rRNA production and promotes tumorigenesis in HCC |
title_sort | tcof1 coordinates oncogenic activation and rrna production and promotes tumorigenesis in hcc |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8819287/ https://www.ncbi.nlm.nih.gov/pubmed/34904330 http://dx.doi.org/10.1111/cas.15242 |
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