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Liriopesides B induces apoptosis and cell cycle arrest in human non-small cell lung cancer cells

Although significant progress has been made in the treatment of lung cancer, it remains the leading cause of cancer-associated mortality. Liriopesides B (LPB) is a natural product isolated from the tuber of Liriope platyphylla, whose effective substances have exhibited antitumor activity in several...

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Autores principales: Sheng, Hongxu, Lv, Wang, Zhu, Linhai, Wang, Luming, Wang, Zhitian, Han, Jia, Hu, Jian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7387084/
https://www.ncbi.nlm.nih.gov/pubmed/32705266
http://dx.doi.org/10.3892/ijmm.2020.4645
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author Sheng, Hongxu
Lv, Wang
Zhu, Linhai
Wang, Luming
Wang, Zhitian
Han, Jia
Hu, Jian
author_facet Sheng, Hongxu
Lv, Wang
Zhu, Linhai
Wang, Luming
Wang, Zhitian
Han, Jia
Hu, Jian
author_sort Sheng, Hongxu
collection PubMed
description Although significant progress has been made in the treatment of lung cancer, it remains the leading cause of cancer-associated mortality. Liriopesides B (LPB) is a natural product isolated from the tuber of Liriope platyphylla, whose effective substances have exhibited antitumor activity in several types of cancer. However, the functions of LPB in non-small cell lung cancer (NSCLC) require further investigation. Therefore, the present study aimed to investigate whether LPB influences the pathogenic effects of NSCLC. In the present study, it was demonstrated that LPB reduced proliferation, and induced apoptosis and cell cycle arrest in non-small cell lung cancer cells. CCK-8 and colony formation assays demonstrated that LPB decreased cell viability and proliferation of H460 and H1975 cells in a dose-dependent manner. Flow cytometry revealed that LPB significantly induced apoptosis of NSCLC cells, along with changes in the expression of apoptosis-associated proteins, including an increase in Bax, caspase-3, and caspase-8 expression, and a decrease in Bcl-2 and Bcl-xl expression. LPB inhibited the progression of the cell cycle from the G1 to the S phase. Furthermore, autophagy was increased in cells treated with LPB. Finally, the expression of programmed death-ligand 1 was significantly decreased by LPB. In conclusion, the results of the present study highlight a potential novel strategy for the clinical treatment of NSCLC.
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spelling pubmed-73870842020-07-31 Liriopesides B induces apoptosis and cell cycle arrest in human non-small cell lung cancer cells Sheng, Hongxu Lv, Wang Zhu, Linhai Wang, Luming Wang, Zhitian Han, Jia Hu, Jian Int J Mol Med Articles Although significant progress has been made in the treatment of lung cancer, it remains the leading cause of cancer-associated mortality. Liriopesides B (LPB) is a natural product isolated from the tuber of Liriope platyphylla, whose effective substances have exhibited antitumor activity in several types of cancer. However, the functions of LPB in non-small cell lung cancer (NSCLC) require further investigation. Therefore, the present study aimed to investigate whether LPB influences the pathogenic effects of NSCLC. In the present study, it was demonstrated that LPB reduced proliferation, and induced apoptosis and cell cycle arrest in non-small cell lung cancer cells. CCK-8 and colony formation assays demonstrated that LPB decreased cell viability and proliferation of H460 and H1975 cells in a dose-dependent manner. Flow cytometry revealed that LPB significantly induced apoptosis of NSCLC cells, along with changes in the expression of apoptosis-associated proteins, including an increase in Bax, caspase-3, and caspase-8 expression, and a decrease in Bcl-2 and Bcl-xl expression. LPB inhibited the progression of the cell cycle from the G1 to the S phase. Furthermore, autophagy was increased in cells treated with LPB. Finally, the expression of programmed death-ligand 1 was significantly decreased by LPB. In conclusion, the results of the present study highlight a potential novel strategy for the clinical treatment of NSCLC. D.A. Spandidos 2020-09 2020-06-16 /pmc/articles/PMC7387084/ /pubmed/32705266 http://dx.doi.org/10.3892/ijmm.2020.4645 Text en Copyright: © Sheng et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Sheng, Hongxu
Lv, Wang
Zhu, Linhai
Wang, Luming
Wang, Zhitian
Han, Jia
Hu, Jian
Liriopesides B induces apoptosis and cell cycle arrest in human non-small cell lung cancer cells
title Liriopesides B induces apoptosis and cell cycle arrest in human non-small cell lung cancer cells
title_full Liriopesides B induces apoptosis and cell cycle arrest in human non-small cell lung cancer cells
title_fullStr Liriopesides B induces apoptosis and cell cycle arrest in human non-small cell lung cancer cells
title_full_unstemmed Liriopesides B induces apoptosis and cell cycle arrest in human non-small cell lung cancer cells
title_short Liriopesides B induces apoptosis and cell cycle arrest in human non-small cell lung cancer cells
title_sort liriopesides b induces apoptosis and cell cycle arrest in human non-small cell lung cancer cells
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7387084/
https://www.ncbi.nlm.nih.gov/pubmed/32705266
http://dx.doi.org/10.3892/ijmm.2020.4645
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