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HLTF promotes hepatocellular carcinoma progression by enhancing SRSF1 stability and activating ERK/MAPK pathway

Helicase-like transcription factor (HLTF) has been found to be involved in the progression of several tumors, but the role of HLTF in hepatocellular carcinoma (HCC) progression has not been studied. Here, our study explored the underlying mechanism of HLTF in HCC progression for the first time. Data...

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Autores principales: Xu, Yanan, Ke, Shanjia, Lu, Shounan, Wang, Chaoqun, Li, Zihao, Feng, Zhigang, Yu, Hongjun, Bai, Miaoyu, Qian, Baolin, Yin, Bing, Li, Xinglong, Hua, Yongliang, Jiang, Hongchi, Ma, Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9859789/
https://www.ncbi.nlm.nih.gov/pubmed/36670110
http://dx.doi.org/10.1038/s41389-023-00447-5
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author Xu, Yanan
Ke, Shanjia
Lu, Shounan
Wang, Chaoqun
Li, Zihao
Feng, Zhigang
Yu, Hongjun
Bai, Miaoyu
Qian, Baolin
Yin, Bing
Li, Xinglong
Hua, Yongliang
Jiang, Hongchi
Ma, Yong
author_facet Xu, Yanan
Ke, Shanjia
Lu, Shounan
Wang, Chaoqun
Li, Zihao
Feng, Zhigang
Yu, Hongjun
Bai, Miaoyu
Qian, Baolin
Yin, Bing
Li, Xinglong
Hua, Yongliang
Jiang, Hongchi
Ma, Yong
author_sort Xu, Yanan
collection PubMed
description Helicase-like transcription factor (HLTF) has been found to be involved in the progression of several tumors, but the role of HLTF in hepatocellular carcinoma (HCC) progression has not been studied. Here, our study explored the underlying mechanism of HLTF in HCC progression for the first time. Database analysis and clinical sample examination indicated that HLTF was upregulated in HCC tissues and was related to poor clinicopathological features in patients. Upregulation of HLTF accelerated the growth and metastasis of HCC cells both in vitro and in vivo. Bioinformatics analysis and subsequent experiments revealed that ERK/MAPK signaling pathway activation was vital to HLTF-mediated proliferation and metastasis in HCC cells. Moreover, HLTF was demonstrated to interact with SRSF1 and contribute to its protein stability to activate the ERK/MAPK signaling pathway and enhance HCC growth and metastasis. In addition, miR-511-5p was expressed at a low level in HCC tissues, was negatively correlated HLTF, and regulated HLTF expression. Our study shows that HLTF plays an oncogenic role in HCC progression and provides a novel biomarker and therapeutic target for the diagnosis and treatment of HCC.
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spelling pubmed-98597892023-01-22 HLTF promotes hepatocellular carcinoma progression by enhancing SRSF1 stability and activating ERK/MAPK pathway Xu, Yanan Ke, Shanjia Lu, Shounan Wang, Chaoqun Li, Zihao Feng, Zhigang Yu, Hongjun Bai, Miaoyu Qian, Baolin Yin, Bing Li, Xinglong Hua, Yongliang Jiang, Hongchi Ma, Yong Oncogenesis Article Helicase-like transcription factor (HLTF) has been found to be involved in the progression of several tumors, but the role of HLTF in hepatocellular carcinoma (HCC) progression has not been studied. Here, our study explored the underlying mechanism of HLTF in HCC progression for the first time. Database analysis and clinical sample examination indicated that HLTF was upregulated in HCC tissues and was related to poor clinicopathological features in patients. Upregulation of HLTF accelerated the growth and metastasis of HCC cells both in vitro and in vivo. Bioinformatics analysis and subsequent experiments revealed that ERK/MAPK signaling pathway activation was vital to HLTF-mediated proliferation and metastasis in HCC cells. Moreover, HLTF was demonstrated to interact with SRSF1 and contribute to its protein stability to activate the ERK/MAPK signaling pathway and enhance HCC growth and metastasis. In addition, miR-511-5p was expressed at a low level in HCC tissues, was negatively correlated HLTF, and regulated HLTF expression. Our study shows that HLTF plays an oncogenic role in HCC progression and provides a novel biomarker and therapeutic target for the diagnosis and treatment of HCC. Nature Publishing Group UK 2023-01-20 /pmc/articles/PMC9859789/ /pubmed/36670110 http://dx.doi.org/10.1038/s41389-023-00447-5 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Xu, Yanan
Ke, Shanjia
Lu, Shounan
Wang, Chaoqun
Li, Zihao
Feng, Zhigang
Yu, Hongjun
Bai, Miaoyu
Qian, Baolin
Yin, Bing
Li, Xinglong
Hua, Yongliang
Jiang, Hongchi
Ma, Yong
HLTF promotes hepatocellular carcinoma progression by enhancing SRSF1 stability and activating ERK/MAPK pathway
title HLTF promotes hepatocellular carcinoma progression by enhancing SRSF1 stability and activating ERK/MAPK pathway
title_full HLTF promotes hepatocellular carcinoma progression by enhancing SRSF1 stability and activating ERK/MAPK pathway
title_fullStr HLTF promotes hepatocellular carcinoma progression by enhancing SRSF1 stability and activating ERK/MAPK pathway
title_full_unstemmed HLTF promotes hepatocellular carcinoma progression by enhancing SRSF1 stability and activating ERK/MAPK pathway
title_short HLTF promotes hepatocellular carcinoma progression by enhancing SRSF1 stability and activating ERK/MAPK pathway
title_sort hltf promotes hepatocellular carcinoma progression by enhancing srsf1 stability and activating erk/mapk pathway
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9859789/
https://www.ncbi.nlm.nih.gov/pubmed/36670110
http://dx.doi.org/10.1038/s41389-023-00447-5
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