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Anticancer activity of Astragalus polysaccharide in human non-small cell lung cancer cells

BACKGROUND: We have reported that Chinese herbs Astragalus polysaccharide (APS) can inhibit nuclear factor kappaB (NF-κB) activity during the development of diabetic nephropathy in mice. NF-κB plays important roles in genesis, growth, development and metastasis of cancer. NF-κB is also involved in t...

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Autores principales: Wu, Chao-Yan, Ke, Yuan, Zeng, Yi-Fei, Zhang, Ying-Wen, Yu, Hai-Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5716001/
https://www.ncbi.nlm.nih.gov/pubmed/29225515
http://dx.doi.org/10.1186/s12935-017-0487-6
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author Wu, Chao-Yan
Ke, Yuan
Zeng, Yi-Fei
Zhang, Ying-Wen
Yu, Hai-Jun
author_facet Wu, Chao-Yan
Ke, Yuan
Zeng, Yi-Fei
Zhang, Ying-Wen
Yu, Hai-Jun
author_sort Wu, Chao-Yan
collection PubMed
description BACKGROUND: We have reported that Chinese herbs Astragalus polysaccharide (APS) can inhibit nuclear factor kappaB (NF-κB) activity during the development of diabetic nephropathy in mice. NF-κB plays important roles in genesis, growth, development and metastasis of cancer. NF-κB is also involved in the development of treatment resistance in tumors. Here we investigated the antitumor activity of APS in human non-small cell lung cells (A549 and NCI-H358) and the related mechanisms of action. METHODS: The dose–effect and time-effect of antitumor of APS were determined in human lung cancer cell line A549 and NCI-H358. The inhibition effect of APS on the P65 mRNA and protein was detected by reverse transcriptase-PCR (RT-PCR) and Western blot in A549 cells respectively. The inhibition effect of APS on the p50, CyclinD1 and Bcl-xL protein was detected by Western blot in A549 cells respectively. The effect of APS on NF-κB transcription activity was measured with NF-κB luciferase detection. Finally, the nude mice A549 xenograft was introduced to confirm the antitumor activity of APS in vivo. RESULTS: Cell viability detection results indicated that APS can inhibit the proliferation of human lung cancer cell line A549 and NCI-H358 in the concentration of 20 and 40 mg/mL. NF-κB activator Phorbol 12-myristate13-acetate (PMA) can attenuate the antitumor activity of APS in both cell lines, but NF-κB inhibitor BAY 11-7082 (Bay) can enhance the effect of APS in both cell lines. In vivo APS can delay the growth of A549 xenograft in BALB/C nude mice. APS can down-regulate the expression of P65 mRNA and protein of A549 cells and decrease the expression of p50, CyclinD1 and Bcl-xL protein. The luciferase detection showed that the APS could reduce the P65 transcription activity in A549 cells. PMA can partially alleviate the inhibition activity of P65 transcription activity of APS in A549 cells, and Bay can enhance the down-regulation of the P65 transcription activity induced by APS in A549 cells. CONCLUSION: APS has a significant antitumor activity in human lung cancer cells A549 and NCI-H358. NF-κB inhibition may mediate the antitumor effect.
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spelling pubmed-57160012017-12-08 Anticancer activity of Astragalus polysaccharide in human non-small cell lung cancer cells Wu, Chao-Yan Ke, Yuan Zeng, Yi-Fei Zhang, Ying-Wen Yu, Hai-Jun Cancer Cell Int Primary Research BACKGROUND: We have reported that Chinese herbs Astragalus polysaccharide (APS) can inhibit nuclear factor kappaB (NF-κB) activity during the development of diabetic nephropathy in mice. NF-κB plays important roles in genesis, growth, development and metastasis of cancer. NF-κB is also involved in the development of treatment resistance in tumors. Here we investigated the antitumor activity of APS in human non-small cell lung cells (A549 and NCI-H358) and the related mechanisms of action. METHODS: The dose–effect and time-effect of antitumor of APS were determined in human lung cancer cell line A549 and NCI-H358. The inhibition effect of APS on the P65 mRNA and protein was detected by reverse transcriptase-PCR (RT-PCR) and Western blot in A549 cells respectively. The inhibition effect of APS on the p50, CyclinD1 and Bcl-xL protein was detected by Western blot in A549 cells respectively. The effect of APS on NF-κB transcription activity was measured with NF-κB luciferase detection. Finally, the nude mice A549 xenograft was introduced to confirm the antitumor activity of APS in vivo. RESULTS: Cell viability detection results indicated that APS can inhibit the proliferation of human lung cancer cell line A549 and NCI-H358 in the concentration of 20 and 40 mg/mL. NF-κB activator Phorbol 12-myristate13-acetate (PMA) can attenuate the antitumor activity of APS in both cell lines, but NF-κB inhibitor BAY 11-7082 (Bay) can enhance the effect of APS in both cell lines. In vivo APS can delay the growth of A549 xenograft in BALB/C nude mice. APS can down-regulate the expression of P65 mRNA and protein of A549 cells and decrease the expression of p50, CyclinD1 and Bcl-xL protein. The luciferase detection showed that the APS could reduce the P65 transcription activity in A549 cells. PMA can partially alleviate the inhibition activity of P65 transcription activity of APS in A549 cells, and Bay can enhance the down-regulation of the P65 transcription activity induced by APS in A549 cells. CONCLUSION: APS has a significant antitumor activity in human lung cancer cells A549 and NCI-H358. NF-κB inhibition may mediate the antitumor effect. BioMed Central 2017-12-04 /pmc/articles/PMC5716001/ /pubmed/29225515 http://dx.doi.org/10.1186/s12935-017-0487-6 Text en © The Author(s) 2017 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 Primary Research
Wu, Chao-Yan
Ke, Yuan
Zeng, Yi-Fei
Zhang, Ying-Wen
Yu, Hai-Jun
Anticancer activity of Astragalus polysaccharide in human non-small cell lung cancer cells
title Anticancer activity of Astragalus polysaccharide in human non-small cell lung cancer cells
title_full Anticancer activity of Astragalus polysaccharide in human non-small cell lung cancer cells
title_fullStr Anticancer activity of Astragalus polysaccharide in human non-small cell lung cancer cells
title_full_unstemmed Anticancer activity of Astragalus polysaccharide in human non-small cell lung cancer cells
title_short Anticancer activity of Astragalus polysaccharide in human non-small cell lung cancer cells
title_sort anticancer activity of astragalus polysaccharide in human non-small cell lung cancer cells
topic Primary Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5716001/
https://www.ncbi.nlm.nih.gov/pubmed/29225515
http://dx.doi.org/10.1186/s12935-017-0487-6
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