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Nujiangexathone A, a Novel Compound Derived from Garcinia nujiangensis, Induces Caspase-Dependent Apoptosis in Cervical Cancer through the ROS/JNK Pathway

Nujiangexathone A (NJXA), a novel compound derived from Garcinia nujiangensis, has been demonstrated to inhibit the proliferation of several human cancer cell lines. This study is the first to demonstrate the apoptosis inductive activities of NJXA and the possible underlying mechanisms. Our results...

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Autores principales: Zhang, Li, Kong, Si-Yuan, Zheng, Zhao-Qing, Meng, Xiao-Xiao, Feng, Ji-Ling, Tan, Hong-Sheng, Lao, Yuan-Zhi, Xiao, Lian-Bo, Xu, Hong-Xi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6274097/
https://www.ncbi.nlm.nih.gov/pubmed/27754347
http://dx.doi.org/10.3390/molecules21101360
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author Zhang, Li
Kong, Si-Yuan
Zheng, Zhao-Qing
Meng, Xiao-Xiao
Feng, Ji-Ling
Tan, Hong-Sheng
Lao, Yuan-Zhi
Xiao, Lian-Bo
Xu, Hong-Xi
author_facet Zhang, Li
Kong, Si-Yuan
Zheng, Zhao-Qing
Meng, Xiao-Xiao
Feng, Ji-Ling
Tan, Hong-Sheng
Lao, Yuan-Zhi
Xiao, Lian-Bo
Xu, Hong-Xi
author_sort Zhang, Li
collection PubMed
description Nujiangexathone A (NJXA), a novel compound derived from Garcinia nujiangensis, has been demonstrated to inhibit the proliferation of several human cancer cell lines. This study is the first to demonstrate the apoptosis inductive activities of NJXA and the possible underlying mechanisms. Our results demonstrated that NJXA inhibited colony formation by HeLa and SiHa cells in a dose-dependent manner. An Annexin V-FITC/PI staining assay showed that NJXA strongly triggered apoptosis in a dose-dependent manner. Western blotting analyses showed that NJXA induced the caspase-dependent apoptosis of HeLa and SiHa cells by triggering a series of events, including changes in the levels of Bcl-2 family proteins, cytochrome c release, caspase-3 activation, and chromosome fragmentation. Furthermore, we demonstrated that NJXA induced cell apoptosis by activating the reactive oxygen species (ROS)-mediated JNK signaling pathway. Consistent with this finding, a ROS scavenger, N-acetyl-l-cysteine (NAC, 10 mM), hindered NJXA-induced apoptosis and attenuated the sensitivity of HeLa and SiHa cells to NJXA. In vivo results further confirmed that the tumor inhibitory effect of NJXA was partially through the induction of apoptosis. Taken together, our results demonstrated that NJXA induced the apoptosis of HeLa and SiHa cells through the ROS/JNK signaling pathway, indicating that NJXA could be important candidate for the clinical treatment of cervical cancer.
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spelling pubmed-62740972018-12-28 Nujiangexathone A, a Novel Compound Derived from Garcinia nujiangensis, Induces Caspase-Dependent Apoptosis in Cervical Cancer through the ROS/JNK Pathway Zhang, Li Kong, Si-Yuan Zheng, Zhao-Qing Meng, Xiao-Xiao Feng, Ji-Ling Tan, Hong-Sheng Lao, Yuan-Zhi Xiao, Lian-Bo Xu, Hong-Xi Molecules Article Nujiangexathone A (NJXA), a novel compound derived from Garcinia nujiangensis, has been demonstrated to inhibit the proliferation of several human cancer cell lines. This study is the first to demonstrate the apoptosis inductive activities of NJXA and the possible underlying mechanisms. Our results demonstrated that NJXA inhibited colony formation by HeLa and SiHa cells in a dose-dependent manner. An Annexin V-FITC/PI staining assay showed that NJXA strongly triggered apoptosis in a dose-dependent manner. Western blotting analyses showed that NJXA induced the caspase-dependent apoptosis of HeLa and SiHa cells by triggering a series of events, including changes in the levels of Bcl-2 family proteins, cytochrome c release, caspase-3 activation, and chromosome fragmentation. Furthermore, we demonstrated that NJXA induced cell apoptosis by activating the reactive oxygen species (ROS)-mediated JNK signaling pathway. Consistent with this finding, a ROS scavenger, N-acetyl-l-cysteine (NAC, 10 mM), hindered NJXA-induced apoptosis and attenuated the sensitivity of HeLa and SiHa cells to NJXA. In vivo results further confirmed that the tumor inhibitory effect of NJXA was partially through the induction of apoptosis. Taken together, our results demonstrated that NJXA induced the apoptosis of HeLa and SiHa cells through the ROS/JNK signaling pathway, indicating that NJXA could be important candidate for the clinical treatment of cervical cancer. MDPI 2016-10-12 /pmc/articles/PMC6274097/ /pubmed/27754347 http://dx.doi.org/10.3390/molecules21101360 Text en © 2016 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Zhang, Li
Kong, Si-Yuan
Zheng, Zhao-Qing
Meng, Xiao-Xiao
Feng, Ji-Ling
Tan, Hong-Sheng
Lao, Yuan-Zhi
Xiao, Lian-Bo
Xu, Hong-Xi
Nujiangexathone A, a Novel Compound Derived from Garcinia nujiangensis, Induces Caspase-Dependent Apoptosis in Cervical Cancer through the ROS/JNK Pathway
title Nujiangexathone A, a Novel Compound Derived from Garcinia nujiangensis, Induces Caspase-Dependent Apoptosis in Cervical Cancer through the ROS/JNK Pathway
title_full Nujiangexathone A, a Novel Compound Derived from Garcinia nujiangensis, Induces Caspase-Dependent Apoptosis in Cervical Cancer through the ROS/JNK Pathway
title_fullStr Nujiangexathone A, a Novel Compound Derived from Garcinia nujiangensis, Induces Caspase-Dependent Apoptosis in Cervical Cancer through the ROS/JNK Pathway
title_full_unstemmed Nujiangexathone A, a Novel Compound Derived from Garcinia nujiangensis, Induces Caspase-Dependent Apoptosis in Cervical Cancer through the ROS/JNK Pathway
title_short Nujiangexathone A, a Novel Compound Derived from Garcinia nujiangensis, Induces Caspase-Dependent Apoptosis in Cervical Cancer through the ROS/JNK Pathway
title_sort nujiangexathone a, a novel compound derived from garcinia nujiangensis, induces caspase-dependent apoptosis in cervical cancer through the ros/jnk pathway
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6274097/
https://www.ncbi.nlm.nih.gov/pubmed/27754347
http://dx.doi.org/10.3390/molecules21101360
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