Cargando…

Trichloromethane fraction of Incarvillea compacta induces lytic cytotoxicity and apoptosis in Epstein-Barr virus-positive gastric cancer AGS cells

BACKGROUND: Incarvillea compacta Maxim. has been used to treat stomach disease in Tibet for many years. The objectives of this study were to explore the anti-cancer ability of trichloromethane fraction of I. compacta Maxim. roots (IC-TCL, R2) in EBV positive AGS cancer cells and its effects on cell...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Lijing, Wu, Haifeng, Sun, Guibo, Xu, Xudong, Sun, Xiaobo, Cao, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5011811/
https://www.ncbi.nlm.nih.gov/pubmed/27595569
http://dx.doi.org/10.1186/s12906-016-1331-6
_version_ 1782451898661470208
author Zhang, Lijing
Wu, Haifeng
Sun, Guibo
Xu, Xudong
Sun, Xiaobo
Cao, Li
author_facet Zhang, Lijing
Wu, Haifeng
Sun, Guibo
Xu, Xudong
Sun, Xiaobo
Cao, Li
author_sort Zhang, Lijing
collection PubMed
description BACKGROUND: Incarvillea compacta Maxim. has been used to treat stomach disease in Tibet for many years. The objectives of this study were to explore the anti-cancer ability of trichloromethane fraction of I. compacta Maxim. roots (IC-TCL, R2) in EBV positive AGS cancer cells and its effects on cell cycle arrest, apoptosis and lytic induction. METHODS: MTT and trypan blue assays were to detect the inhibitory effects of different fraction in different cell lines. Hoechst 33342 staining, Annexin V-PE/7-AAD staining and DIOC(6) staining were used to detect the apoptosis induction effects of R2. Western blot experiments were used to detect the expression of apoptosis related proteins BAX and Bcl-2, EBV lytic related proteins BZLF1 and BMRF1, cell cycle regulation related proteins Cyclin D1 and RB after R2 treatment. Cell cycle arrest was analyzed by flow cytometry. RESULTS: MTT and trypan blue assays revealed that R2 could significantly reduce cell viability in a dose-dependent manner in EBV positive AGS cells compared with non-EBV infected AGS and other cancer cell lines, whereas n-BuOH and H(2)O fractions showed non-inhibitory effects in tested cancer cells. R2 could decrease mitochondrial membrane potential and the expression of Bcl-2, while increase the expression of BAX. R2 could also induce EBV lytic replication by activating mRNA levels of BZLF1, BRLF1 and BMRF1. Protein expressions of BZLF1 and BMRF1 were also increased after R2 treatment. Cell cycle analysis showed that R2 treatment could induce G0/G1 phase arrest. The expression of Cyclin D1 decreased, while Rb increased. CONCLUSIONS: These results demonstrated that R2 could inhibit the proliferation of AGS-EBV cancer cells by inducing EBV lytic replication, apoptosis and G0/G1 arrest, through the regulation of related proteins. Therefore, R2 could be used as a potential treatment in AGS-EBV cells. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12906-016-1331-6) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-5011811
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-50118112016-09-07 Trichloromethane fraction of Incarvillea compacta induces lytic cytotoxicity and apoptosis in Epstein-Barr virus-positive gastric cancer AGS cells Zhang, Lijing Wu, Haifeng Sun, Guibo Xu, Xudong Sun, Xiaobo Cao, Li BMC Complement Altern Med Research Article BACKGROUND: Incarvillea compacta Maxim. has been used to treat stomach disease in Tibet for many years. The objectives of this study were to explore the anti-cancer ability of trichloromethane fraction of I. compacta Maxim. roots (IC-TCL, R2) in EBV positive AGS cancer cells and its effects on cell cycle arrest, apoptosis and lytic induction. METHODS: MTT and trypan blue assays were to detect the inhibitory effects of different fraction in different cell lines. Hoechst 33342 staining, Annexin V-PE/7-AAD staining and DIOC(6) staining were used to detect the apoptosis induction effects of R2. Western blot experiments were used to detect the expression of apoptosis related proteins BAX and Bcl-2, EBV lytic related proteins BZLF1 and BMRF1, cell cycle regulation related proteins Cyclin D1 and RB after R2 treatment. Cell cycle arrest was analyzed by flow cytometry. RESULTS: MTT and trypan blue assays revealed that R2 could significantly reduce cell viability in a dose-dependent manner in EBV positive AGS cells compared with non-EBV infected AGS and other cancer cell lines, whereas n-BuOH and H(2)O fractions showed non-inhibitory effects in tested cancer cells. R2 could decrease mitochondrial membrane potential and the expression of Bcl-2, while increase the expression of BAX. R2 could also induce EBV lytic replication by activating mRNA levels of BZLF1, BRLF1 and BMRF1. Protein expressions of BZLF1 and BMRF1 were also increased after R2 treatment. Cell cycle analysis showed that R2 treatment could induce G0/G1 phase arrest. The expression of Cyclin D1 decreased, while Rb increased. CONCLUSIONS: These results demonstrated that R2 could inhibit the proliferation of AGS-EBV cancer cells by inducing EBV lytic replication, apoptosis and G0/G1 arrest, through the regulation of related proteins. Therefore, R2 could be used as a potential treatment in AGS-EBV cells. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12906-016-1331-6) contains supplementary material, which is available to authorized users. BioMed Central 2016-09-05 /pmc/articles/PMC5011811/ /pubmed/27595569 http://dx.doi.org/10.1186/s12906-016-1331-6 Text en © The Author(s). 2016 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 Article
Zhang, Lijing
Wu, Haifeng
Sun, Guibo
Xu, Xudong
Sun, Xiaobo
Cao, Li
Trichloromethane fraction of Incarvillea compacta induces lytic cytotoxicity and apoptosis in Epstein-Barr virus-positive gastric cancer AGS cells
title Trichloromethane fraction of Incarvillea compacta induces lytic cytotoxicity and apoptosis in Epstein-Barr virus-positive gastric cancer AGS cells
title_full Trichloromethane fraction of Incarvillea compacta induces lytic cytotoxicity and apoptosis in Epstein-Barr virus-positive gastric cancer AGS cells
title_fullStr Trichloromethane fraction of Incarvillea compacta induces lytic cytotoxicity and apoptosis in Epstein-Barr virus-positive gastric cancer AGS cells
title_full_unstemmed Trichloromethane fraction of Incarvillea compacta induces lytic cytotoxicity and apoptosis in Epstein-Barr virus-positive gastric cancer AGS cells
title_short Trichloromethane fraction of Incarvillea compacta induces lytic cytotoxicity and apoptosis in Epstein-Barr virus-positive gastric cancer AGS cells
title_sort trichloromethane fraction of incarvillea compacta induces lytic cytotoxicity and apoptosis in epstein-barr virus-positive gastric cancer ags cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5011811/
https://www.ncbi.nlm.nih.gov/pubmed/27595569
http://dx.doi.org/10.1186/s12906-016-1331-6
work_keys_str_mv AT zhanglijing trichloromethanefractionofincarvilleacompactainduceslyticcytotoxicityandapoptosisinepsteinbarrviruspositivegastriccanceragscells
AT wuhaifeng trichloromethanefractionofincarvilleacompactainduceslyticcytotoxicityandapoptosisinepsteinbarrviruspositivegastriccanceragscells
AT sunguibo trichloromethanefractionofincarvilleacompactainduceslyticcytotoxicityandapoptosisinepsteinbarrviruspositivegastriccanceragscells
AT xuxudong trichloromethanefractionofincarvilleacompactainduceslyticcytotoxicityandapoptosisinepsteinbarrviruspositivegastriccanceragscells
AT sunxiaobo trichloromethanefractionofincarvilleacompactainduceslyticcytotoxicityandapoptosisinepsteinbarrviruspositivegastriccanceragscells
AT caoli trichloromethanefractionofincarvilleacompactainduceslyticcytotoxicityandapoptosisinepsteinbarrviruspositivegastriccanceragscells