Cargando…

A natural chalcone induces apoptosis in lung cancer cells: 3D-QSAR, docking and an in vivo/vitro assay

This study was to study the antitumor effect of lonchocarpin (34) from traditional herbal medicine Pongamia pinnata (L.) Pierre and to reveal the underlying mechanism. The cytotoxic activities of lonchocarpin were evaluated in 10 lung cancer cell lines and it exhibited 97.5% activity at a dose of 10...

Descripción completa

Detalles Bibliográficos
Autores principales: Chen, Gang, Zhou, Di, Li, Xue-Zheng, Jiang, Zhe, Tan, Chengyu, Wei, Xiu-Yan, Ling, Junhong, Jing, Jing, Liu, Fen, Li, Ning
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5587747/
https://www.ncbi.nlm.nih.gov/pubmed/28878321
http://dx.doi.org/10.1038/s41598-017-11369-9
_version_ 1783262051834003456
author Chen, Gang
Zhou, Di
Li, Xue-Zheng
Jiang, Zhe
Tan, Chengyu
Wei, Xiu-Yan
Ling, Junhong
Jing, Jing
Liu, Fen
Li, Ning
author_facet Chen, Gang
Zhou, Di
Li, Xue-Zheng
Jiang, Zhe
Tan, Chengyu
Wei, Xiu-Yan
Ling, Junhong
Jing, Jing
Liu, Fen
Li, Ning
author_sort Chen, Gang
collection PubMed
description This study was to study the antitumor effect of lonchocarpin (34) from traditional herbal medicine Pongamia pinnata (L.) Pierre and to reveal the underlying mechanism. The cytotoxic activities of lonchocarpin were evaluated in 10 lung cancer cell lines and it exhibited 97.5% activity at a dose of 100 μM in the H292 cell line. A field-based quantitative structure-activity relationship (3D-QSAR) study of 37 flavonoids from P. pinnata was also performed, and the results obtained showed that the hydrophobic interaction could be the crucial factor for the antitumor activity of lonchocarpin. Molecular docking studies revealed that lonchocarpin bound stably to the BH3-binding groove of the Bcl-2 protein with hydrophobic interactions with ALA146. Also, lonchocarpin significantly reduced cell proliferation via modulating Bax/Caspase-9/Caspase-3 pathway. An apoptotic test using flow cytometry showed that lonchocarpin produced about 41.1% and 47.9% apoptosis after treatment for 24 h and 48 h, respectively. Moreover, lonchocarpin inhibited tumor growth in S180-bearing mice with an inhibition rate of 57.94, 63.40 and 72.51%, respectively at a dose of 25, 50 and 100 mg/kg. These results suggest that lonchocarpin is a potentially useful natural agent for cancer treatment.
format Online
Article
Text
id pubmed-5587747
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-55877472017-09-13 A natural chalcone induces apoptosis in lung cancer cells: 3D-QSAR, docking and an in vivo/vitro assay Chen, Gang Zhou, Di Li, Xue-Zheng Jiang, Zhe Tan, Chengyu Wei, Xiu-Yan Ling, Junhong Jing, Jing Liu, Fen Li, Ning Sci Rep Article This study was to study the antitumor effect of lonchocarpin (34) from traditional herbal medicine Pongamia pinnata (L.) Pierre and to reveal the underlying mechanism. The cytotoxic activities of lonchocarpin were evaluated in 10 lung cancer cell lines and it exhibited 97.5% activity at a dose of 100 μM in the H292 cell line. A field-based quantitative structure-activity relationship (3D-QSAR) study of 37 flavonoids from P. pinnata was also performed, and the results obtained showed that the hydrophobic interaction could be the crucial factor for the antitumor activity of lonchocarpin. Molecular docking studies revealed that lonchocarpin bound stably to the BH3-binding groove of the Bcl-2 protein with hydrophobic interactions with ALA146. Also, lonchocarpin significantly reduced cell proliferation via modulating Bax/Caspase-9/Caspase-3 pathway. An apoptotic test using flow cytometry showed that lonchocarpin produced about 41.1% and 47.9% apoptosis after treatment for 24 h and 48 h, respectively. Moreover, lonchocarpin inhibited tumor growth in S180-bearing mice with an inhibition rate of 57.94, 63.40 and 72.51%, respectively at a dose of 25, 50 and 100 mg/kg. These results suggest that lonchocarpin is a potentially useful natural agent for cancer treatment. Nature Publishing Group UK 2017-09-06 /pmc/articles/PMC5587747/ /pubmed/28878321 http://dx.doi.org/10.1038/s41598-017-11369-9 Text en © The Author(s) 2017 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/.
spellingShingle Article
Chen, Gang
Zhou, Di
Li, Xue-Zheng
Jiang, Zhe
Tan, Chengyu
Wei, Xiu-Yan
Ling, Junhong
Jing, Jing
Liu, Fen
Li, Ning
A natural chalcone induces apoptosis in lung cancer cells: 3D-QSAR, docking and an in vivo/vitro assay
title A natural chalcone induces apoptosis in lung cancer cells: 3D-QSAR, docking and an in vivo/vitro assay
title_full A natural chalcone induces apoptosis in lung cancer cells: 3D-QSAR, docking and an in vivo/vitro assay
title_fullStr A natural chalcone induces apoptosis in lung cancer cells: 3D-QSAR, docking and an in vivo/vitro assay
title_full_unstemmed A natural chalcone induces apoptosis in lung cancer cells: 3D-QSAR, docking and an in vivo/vitro assay
title_short A natural chalcone induces apoptosis in lung cancer cells: 3D-QSAR, docking and an in vivo/vitro assay
title_sort natural chalcone induces apoptosis in lung cancer cells: 3d-qsar, docking and an in vivo/vitro assay
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5587747/
https://www.ncbi.nlm.nih.gov/pubmed/28878321
http://dx.doi.org/10.1038/s41598-017-11369-9
work_keys_str_mv AT chengang anaturalchalconeinducesapoptosisinlungcancercells3dqsardockingandaninvivovitroassay
AT zhoudi anaturalchalconeinducesapoptosisinlungcancercells3dqsardockingandaninvivovitroassay
AT lixuezheng anaturalchalconeinducesapoptosisinlungcancercells3dqsardockingandaninvivovitroassay
AT jiangzhe anaturalchalconeinducesapoptosisinlungcancercells3dqsardockingandaninvivovitroassay
AT tanchengyu anaturalchalconeinducesapoptosisinlungcancercells3dqsardockingandaninvivovitroassay
AT weixiuyan anaturalchalconeinducesapoptosisinlungcancercells3dqsardockingandaninvivovitroassay
AT lingjunhong anaturalchalconeinducesapoptosisinlungcancercells3dqsardockingandaninvivovitroassay
AT jingjing anaturalchalconeinducesapoptosisinlungcancercells3dqsardockingandaninvivovitroassay
AT liufen anaturalchalconeinducesapoptosisinlungcancercells3dqsardockingandaninvivovitroassay
AT lining anaturalchalconeinducesapoptosisinlungcancercells3dqsardockingandaninvivovitroassay
AT chengang naturalchalconeinducesapoptosisinlungcancercells3dqsardockingandaninvivovitroassay
AT zhoudi naturalchalconeinducesapoptosisinlungcancercells3dqsardockingandaninvivovitroassay
AT lixuezheng naturalchalconeinducesapoptosisinlungcancercells3dqsardockingandaninvivovitroassay
AT jiangzhe naturalchalconeinducesapoptosisinlungcancercells3dqsardockingandaninvivovitroassay
AT tanchengyu naturalchalconeinducesapoptosisinlungcancercells3dqsardockingandaninvivovitroassay
AT weixiuyan naturalchalconeinducesapoptosisinlungcancercells3dqsardockingandaninvivovitroassay
AT lingjunhong naturalchalconeinducesapoptosisinlungcancercells3dqsardockingandaninvivovitroassay
AT jingjing naturalchalconeinducesapoptosisinlungcancercells3dqsardockingandaninvivovitroassay
AT liufen naturalchalconeinducesapoptosisinlungcancercells3dqsardockingandaninvivovitroassay
AT lining naturalchalconeinducesapoptosisinlungcancercells3dqsardockingandaninvivovitroassay