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Elevation of EIF4G1 promotes non‐small cell lung cancer progression by activating mTOR signalling
Eukaryotic translation initiation factor 4 gamma 1 (EIF4G1), as the key component of the transcription initiation factor complex EIF4F, is significantly upregulated in multiple solid tumours, including lung cancer. However, the function and mechanism of EIF4G1 in the regulation of non‐small‐cell lun...
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/PMC7957198/ https://www.ncbi.nlm.nih.gov/pubmed/33523588 http://dx.doi.org/10.1111/jcmm.16340 |
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author | Lu, Ying Yu, Shanshan Wang, Guangxue Ma, Zuan Fu, Xuelian Cao, Yueyu Li, Qinchuan Xu, Zengguang |
author_facet | Lu, Ying Yu, Shanshan Wang, Guangxue Ma, Zuan Fu, Xuelian Cao, Yueyu Li, Qinchuan Xu, Zengguang |
author_sort | Lu, Ying |
collection | PubMed |
description | Eukaryotic translation initiation factor 4 gamma 1 (EIF4G1), as the key component of the transcription initiation factor complex EIF4F, is significantly upregulated in multiple solid tumours, including lung cancer. However, the function and mechanism of EIF4G1 in the regulation of non‐small‐cell lung cancer (NSCLC) remain unclear. Here, using the clinical samples and the comprehensive survival analysis platforms Kaplan‐Meier plotter, we observed aberrant upregulation of EIF4G1 in NSCLC tissues; furthermore, high expression of EIF4G1 showed association with low differentiation of lung cancer cells and poor overall survival in NSCLC patients. Non‐small‐cell lung cancer cell line A549 and H1703 stably infected with EIF4G1 shRNA were used to determine the function of EIF4G1 in regulating cell proliferation and tumorigenesis in vitro and in vivo. The results demonstrated that EIF4G1 promoted the G1/S transition of the cell cycle and tumour cell proliferation in non‐small cell lung cancer. Mechanistically, EIF4G1 was found to regulate the expression and phosphorylation of mTOR (Ser2448), which mediates the tumorigenesis‐promoting function of EIF4G1. The inhibition of mTOR attenuated the EIF4G1‐induced development and progression of tumours. These findings demonstrated that EIF4G1 is a new potential molecular target for the clinical treatment of non‐small cell lung cancer. |
format | Online Article Text |
id | pubmed-7957198 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-79571982021-03-19 Elevation of EIF4G1 promotes non‐small cell lung cancer progression by activating mTOR signalling Lu, Ying Yu, Shanshan Wang, Guangxue Ma, Zuan Fu, Xuelian Cao, Yueyu Li, Qinchuan Xu, Zengguang J Cell Mol Med Original Articles Eukaryotic translation initiation factor 4 gamma 1 (EIF4G1), as the key component of the transcription initiation factor complex EIF4F, is significantly upregulated in multiple solid tumours, including lung cancer. However, the function and mechanism of EIF4G1 in the regulation of non‐small‐cell lung cancer (NSCLC) remain unclear. Here, using the clinical samples and the comprehensive survival analysis platforms Kaplan‐Meier plotter, we observed aberrant upregulation of EIF4G1 in NSCLC tissues; furthermore, high expression of EIF4G1 showed association with low differentiation of lung cancer cells and poor overall survival in NSCLC patients. Non‐small‐cell lung cancer cell line A549 and H1703 stably infected with EIF4G1 shRNA were used to determine the function of EIF4G1 in regulating cell proliferation and tumorigenesis in vitro and in vivo. The results demonstrated that EIF4G1 promoted the G1/S transition of the cell cycle and tumour cell proliferation in non‐small cell lung cancer. Mechanistically, EIF4G1 was found to regulate the expression and phosphorylation of mTOR (Ser2448), which mediates the tumorigenesis‐promoting function of EIF4G1. The inhibition of mTOR attenuated the EIF4G1‐induced development and progression of tumours. These findings demonstrated that EIF4G1 is a new potential molecular target for the clinical treatment of non‐small cell lung cancer. John Wiley and Sons Inc. 2021-02-01 2021-03 /pmc/articles/PMC7957198/ /pubmed/33523588 http://dx.doi.org/10.1111/jcmm.16340 Text en © 2021 The Authors. Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Lu, Ying Yu, Shanshan Wang, Guangxue Ma, Zuan Fu, Xuelian Cao, Yueyu Li, Qinchuan Xu, Zengguang Elevation of EIF4G1 promotes non‐small cell lung cancer progression by activating mTOR signalling |
title | Elevation of EIF4G1 promotes non‐small cell lung cancer progression by activating mTOR signalling |
title_full | Elevation of EIF4G1 promotes non‐small cell lung cancer progression by activating mTOR signalling |
title_fullStr | Elevation of EIF4G1 promotes non‐small cell lung cancer progression by activating mTOR signalling |
title_full_unstemmed | Elevation of EIF4G1 promotes non‐small cell lung cancer progression by activating mTOR signalling |
title_short | Elevation of EIF4G1 promotes non‐small cell lung cancer progression by activating mTOR signalling |
title_sort | elevation of eif4g1 promotes non‐small cell lung cancer progression by activating mtor signalling |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7957198/ https://www.ncbi.nlm.nih.gov/pubmed/33523588 http://dx.doi.org/10.1111/jcmm.16340 |
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