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Rhein sensitizes human pancreatic cancer cells to EGFR inhibitors by inhibiting STAT3 pathway
BACKGROUND: Rhein is a lipophilic anthraquinone extensively found in medicinal herbs. Emerging evidence suggests that rhein has significant antitumor effects, supporting its potential use as an antitumor agent. The IL6/STAT3 signaling pathway has been suggested as an attractive target for the discov...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6343257/ https://www.ncbi.nlm.nih.gov/pubmed/30674340 http://dx.doi.org/10.1186/s13046-018-1015-9 |
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author | Yang, Lehe Lin, Shichong Kang, Yanting Xiang, Youqun Xu, Lingyuan Li, Jifa Dai, Xuanxuan Liang, Guang Huang, Xiaoying Zhao, Chengguang |
author_facet | Yang, Lehe Lin, Shichong Kang, Yanting Xiang, Youqun Xu, Lingyuan Li, Jifa Dai, Xuanxuan Liang, Guang Huang, Xiaoying Zhao, Chengguang |
author_sort | Yang, Lehe |
collection | PubMed |
description | BACKGROUND: Rhein is a lipophilic anthraquinone extensively found in medicinal herbs. Emerging evidence suggests that rhein has significant antitumor effects, supporting its potential use as an antitumor agent. The IL6/STAT3 signaling pathway has been suggested as an attractive target for the discovery of novel cancer therapeutics. METHODS: The human pancreatic cancer cell lines AsPC-1, Patu8988T, BxPC-3 and PANC-1, and immunodeficient mice were chosen as models to study the effects of rhein. The potent antiproliferative and proapoptotic effects of rhein were examined by cell viability, cellular morphology, apoptosis and colony formation assays. The STAT3 luciferase report assay, immunostaining analysis and Western blot analysis revealed the inhibition of the IL6/STAT3 signaling axis. RESULTS: Apoptosis was induced by adjunctive use of rhein with epidermal growth factor receptor (EGFR) inhibitors in pancreatic cancer cells as verified by cell apoptosis analysis and changes in the expression level of apoptotic/anti-apoptotic proteins BCL-2, BAX, Caspase 3 and Cl-PARP. Suppression of the phosphorylation of STAT3 and EGFR were also observed as a result of the treatment with a combination of rhein and EGFR inhibitors. Most interestingly, it was found that rhein considerably sensitized cells to erlotinib, thus suppressing tumor growth in PANC-1 and BxPC-3 xenograft models. The in vivo anti-tumor effect was associated with increased apoptosis and combined inhibition of the STAT3 and EGFR pathways in tumor remnants. CONCLUSIONS: Rhein sensitizes human pancreatic cancer cells to EGFR inhibitors through inhibition of STAT3. Taken together, the results indicate that rhein offers a novel blueprint for pancreatic cancer therapy, particularly when combined with EGFR inhibitors. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13046-018-1015-9) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6343257 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-63432572019-01-24 Rhein sensitizes human pancreatic cancer cells to EGFR inhibitors by inhibiting STAT3 pathway Yang, Lehe Lin, Shichong Kang, Yanting Xiang, Youqun Xu, Lingyuan Li, Jifa Dai, Xuanxuan Liang, Guang Huang, Xiaoying Zhao, Chengguang J Exp Clin Cancer Res Research BACKGROUND: Rhein is a lipophilic anthraquinone extensively found in medicinal herbs. Emerging evidence suggests that rhein has significant antitumor effects, supporting its potential use as an antitumor agent. The IL6/STAT3 signaling pathway has been suggested as an attractive target for the discovery of novel cancer therapeutics. METHODS: The human pancreatic cancer cell lines AsPC-1, Patu8988T, BxPC-3 and PANC-1, and immunodeficient mice were chosen as models to study the effects of rhein. The potent antiproliferative and proapoptotic effects of rhein were examined by cell viability, cellular morphology, apoptosis and colony formation assays. The STAT3 luciferase report assay, immunostaining analysis and Western blot analysis revealed the inhibition of the IL6/STAT3 signaling axis. RESULTS: Apoptosis was induced by adjunctive use of rhein with epidermal growth factor receptor (EGFR) inhibitors in pancreatic cancer cells as verified by cell apoptosis analysis and changes in the expression level of apoptotic/anti-apoptotic proteins BCL-2, BAX, Caspase 3 and Cl-PARP. Suppression of the phosphorylation of STAT3 and EGFR were also observed as a result of the treatment with a combination of rhein and EGFR inhibitors. Most interestingly, it was found that rhein considerably sensitized cells to erlotinib, thus suppressing tumor growth in PANC-1 and BxPC-3 xenograft models. The in vivo anti-tumor effect was associated with increased apoptosis and combined inhibition of the STAT3 and EGFR pathways in tumor remnants. CONCLUSIONS: Rhein sensitizes human pancreatic cancer cells to EGFR inhibitors through inhibition of STAT3. Taken together, the results indicate that rhein offers a novel blueprint for pancreatic cancer therapy, particularly when combined with EGFR inhibitors. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13046-018-1015-9) contains supplementary material, which is available to authorized users. BioMed Central 2019-01-23 /pmc/articles/PMC6343257/ /pubmed/30674340 http://dx.doi.org/10.1186/s13046-018-1015-9 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Yang, Lehe Lin, Shichong Kang, Yanting Xiang, Youqun Xu, Lingyuan Li, Jifa Dai, Xuanxuan Liang, Guang Huang, Xiaoying Zhao, Chengguang Rhein sensitizes human pancreatic cancer cells to EGFR inhibitors by inhibiting STAT3 pathway |
title | Rhein sensitizes human pancreatic cancer cells to EGFR inhibitors by inhibiting STAT3 pathway |
title_full | Rhein sensitizes human pancreatic cancer cells to EGFR inhibitors by inhibiting STAT3 pathway |
title_fullStr | Rhein sensitizes human pancreatic cancer cells to EGFR inhibitors by inhibiting STAT3 pathway |
title_full_unstemmed | Rhein sensitizes human pancreatic cancer cells to EGFR inhibitors by inhibiting STAT3 pathway |
title_short | Rhein sensitizes human pancreatic cancer cells to EGFR inhibitors by inhibiting STAT3 pathway |
title_sort | rhein sensitizes human pancreatic cancer cells to egfr inhibitors by inhibiting stat3 pathway |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6343257/ https://www.ncbi.nlm.nih.gov/pubmed/30674340 http://dx.doi.org/10.1186/s13046-018-1015-9 |
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