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TLR4 increases the stemness and is highly expressed in relapsed human hepatocellular carcinoma
Toll‐like receptor 4 (TLR4) plays an essential role in cancer progress. Here, we find that the expression of TLR4 in relapsed human hepatocellular carcinoma (HCC) clinical samples is higher than that in the non‐relapsed ones, which leads us to explore the role of TLR4 in cancer stemness. We reported...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6536932/ https://www.ncbi.nlm.nih.gov/pubmed/30957973 http://dx.doi.org/10.1002/cam4.2070 |
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author | Zhou, Shuang Du, Renle Wang, Zhenglu Shen, Wenzhi Gao, Ruifang Jiang, Shan Fang, Yan Shi, Yuzhi Chang, Antao Liu, Lei Liu, Chenghu Li, Na Xiang, Rong |
author_facet | Zhou, Shuang Du, Renle Wang, Zhenglu Shen, Wenzhi Gao, Ruifang Jiang, Shan Fang, Yan Shi, Yuzhi Chang, Antao Liu, Lei Liu, Chenghu Li, Na Xiang, Rong |
author_sort | Zhou, Shuang |
collection | PubMed |
description | Toll‐like receptor 4 (TLR4) plays an essential role in cancer progress. Here, we find that the expression of TLR4 in relapsed human hepatocellular carcinoma (HCC) clinical samples is higher than that in the non‐relapsed ones, which leads us to explore the role of TLR4 in cancer stemness. We reported that TLR4‐AKT signaling pathway was activated by lipopolysaccharides (LPS) in HCC cell lines to enhance the cancer stemness capacity, which was reflected by the increased percentage of CD133(+) CD49f(+) population and side population, enhanced sphere formation, and the upregulation of stemness marker gene‐SOX2. Downregulation of SOX2 attenuated the enhanced HCC stemness induced by LPS, indicating SOX2 as a downstream mediator of LPS‐TLR4 signaling. The role of LPS‐TLR4 signaling in inducing HCC stemness was further confirmed by tumor xenograft experiment in vivo. Taken together, our findings provide a novel therapeutic target to prevent the recurrence of HCC. |
format | Online Article Text |
id | pubmed-6536932 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-65369322019-06-03 TLR4 increases the stemness and is highly expressed in relapsed human hepatocellular carcinoma Zhou, Shuang Du, Renle Wang, Zhenglu Shen, Wenzhi Gao, Ruifang Jiang, Shan Fang, Yan Shi, Yuzhi Chang, Antao Liu, Lei Liu, Chenghu Li, Na Xiang, Rong Cancer Med Cancer Biology Toll‐like receptor 4 (TLR4) plays an essential role in cancer progress. Here, we find that the expression of TLR4 in relapsed human hepatocellular carcinoma (HCC) clinical samples is higher than that in the non‐relapsed ones, which leads us to explore the role of TLR4 in cancer stemness. We reported that TLR4‐AKT signaling pathway was activated by lipopolysaccharides (LPS) in HCC cell lines to enhance the cancer stemness capacity, which was reflected by the increased percentage of CD133(+) CD49f(+) population and side population, enhanced sphere formation, and the upregulation of stemness marker gene‐SOX2. Downregulation of SOX2 attenuated the enhanced HCC stemness induced by LPS, indicating SOX2 as a downstream mediator of LPS‐TLR4 signaling. The role of LPS‐TLR4 signaling in inducing HCC stemness was further confirmed by tumor xenograft experiment in vivo. Taken together, our findings provide a novel therapeutic target to prevent the recurrence of HCC. John Wiley and Sons Inc. 2019-04-08 /pmc/articles/PMC6536932/ /pubmed/30957973 http://dx.doi.org/10.1002/cam4.2070 Text en © 2019 The Authors. Cancer Medicine published by 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 | Cancer Biology Zhou, Shuang Du, Renle Wang, Zhenglu Shen, Wenzhi Gao, Ruifang Jiang, Shan Fang, Yan Shi, Yuzhi Chang, Antao Liu, Lei Liu, Chenghu Li, Na Xiang, Rong TLR4 increases the stemness and is highly expressed in relapsed human hepatocellular carcinoma |
title |
TLR4 increases the stemness and is highly expressed in relapsed human hepatocellular carcinoma |
title_full |
TLR4 increases the stemness and is highly expressed in relapsed human hepatocellular carcinoma |
title_fullStr |
TLR4 increases the stemness and is highly expressed in relapsed human hepatocellular carcinoma |
title_full_unstemmed |
TLR4 increases the stemness and is highly expressed in relapsed human hepatocellular carcinoma |
title_short |
TLR4 increases the stemness and is highly expressed in relapsed human hepatocellular carcinoma |
title_sort | tlr4 increases the stemness and is highly expressed in relapsed human hepatocellular carcinoma |
topic | Cancer Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6536932/ https://www.ncbi.nlm.nih.gov/pubmed/30957973 http://dx.doi.org/10.1002/cam4.2070 |
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