Cargando…

Potential Therapeutic Role of Hispidulin in Gastric Cancer through Induction of Apoptosis via NAG-1 Signaling

Gastric cancer is one of the most common malignant cancers due to poor prognoses and high mortality rates worldwide. However, an effective chemotherapeutic drug without side effects remains lacking. Saussurea involucrata (SI) Kar. et Kir., also known as snow lotus, grows in mountainous rocky habitat...

Descripción completa

Detalles Bibliográficos
Autores principales: Yu, Chao Yuan, Su, Kang-Yi, Lee, Po-Lei, Jhan, Jie-Yu, Tsao, Po-Hung, Chan, De-Chuan, Chen, Yi-Lin Sophia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3789485/
https://www.ncbi.nlm.nih.gov/pubmed/24159347
http://dx.doi.org/10.1155/2013/518301
_version_ 1782286454127329280
author Yu, Chao Yuan
Su, Kang-Yi
Lee, Po-Lei
Jhan, Jie-Yu
Tsao, Po-Hung
Chan, De-Chuan
Chen, Yi-Lin Sophia
author_facet Yu, Chao Yuan
Su, Kang-Yi
Lee, Po-Lei
Jhan, Jie-Yu
Tsao, Po-Hung
Chan, De-Chuan
Chen, Yi-Lin Sophia
author_sort Yu, Chao Yuan
collection PubMed
description Gastric cancer is one of the most common malignant cancers due to poor prognoses and high mortality rates worldwide. However, an effective chemotherapeutic drug without side effects remains lacking. Saussurea involucrata (SI) Kar. et Kir., also known as snow lotus, grows in mountainous rocky habitats at 2600 m elevation in the Tian Shan and A'er Tai regions of China. The ethyl acetate extract of SI had been shown to inhibit proliferation and induce apoptosis in various tumor cells. In this study, we demonstrated that Hispidulin, active ingredients in SI, inhibits the growth of AGS gastric cancer cells. After Hispidulin treatment, NAG-1 remained highly expressed, whereas COX-2 expression was downregulated. Flow cytometric analysis indicated that Hispidulin induces G1/S phase arrest and apoptosis in time- and concentration-dependent manners. G1/S arrest correlated with upregulated p21/WAF1 and p16 and downregulated cyclin D1 and cyclin E, independent of p53 pathway. In addition, Hispidulin can elevate Egr-1 expression and ERK1/2 activity, whereas ERK1/2 inhibitor markedly attenuated NAG-1 mediated apoptosis. Taken together, Hispidulin can efficiently activate ERK1/2 signaling followed by NAG-1 constitutive expression and trigger cell cycle arrest as well as apoptosis in cancer cell. It can be a potential compound for combination therapy of gastric cancer in the future.
format Online
Article
Text
id pubmed-3789485
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Hindawi Publishing Corporation
record_format MEDLINE/PubMed
spelling pubmed-37894852013-10-24 Potential Therapeutic Role of Hispidulin in Gastric Cancer through Induction of Apoptosis via NAG-1 Signaling Yu, Chao Yuan Su, Kang-Yi Lee, Po-Lei Jhan, Jie-Yu Tsao, Po-Hung Chan, De-Chuan Chen, Yi-Lin Sophia Evid Based Complement Alternat Med Research Article Gastric cancer is one of the most common malignant cancers due to poor prognoses and high mortality rates worldwide. However, an effective chemotherapeutic drug without side effects remains lacking. Saussurea involucrata (SI) Kar. et Kir., also known as snow lotus, grows in mountainous rocky habitats at 2600 m elevation in the Tian Shan and A'er Tai regions of China. The ethyl acetate extract of SI had been shown to inhibit proliferation and induce apoptosis in various tumor cells. In this study, we demonstrated that Hispidulin, active ingredients in SI, inhibits the growth of AGS gastric cancer cells. After Hispidulin treatment, NAG-1 remained highly expressed, whereas COX-2 expression was downregulated. Flow cytometric analysis indicated that Hispidulin induces G1/S phase arrest and apoptosis in time- and concentration-dependent manners. G1/S arrest correlated with upregulated p21/WAF1 and p16 and downregulated cyclin D1 and cyclin E, independent of p53 pathway. In addition, Hispidulin can elevate Egr-1 expression and ERK1/2 activity, whereas ERK1/2 inhibitor markedly attenuated NAG-1 mediated apoptosis. Taken together, Hispidulin can efficiently activate ERK1/2 signaling followed by NAG-1 constitutive expression and trigger cell cycle arrest as well as apoptosis in cancer cell. It can be a potential compound for combination therapy of gastric cancer in the future. Hindawi Publishing Corporation 2013 2013-09-15 /pmc/articles/PMC3789485/ /pubmed/24159347 http://dx.doi.org/10.1155/2013/518301 Text en Copyright © 2013 Chao Yuan Yu et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Yu, Chao Yuan
Su, Kang-Yi
Lee, Po-Lei
Jhan, Jie-Yu
Tsao, Po-Hung
Chan, De-Chuan
Chen, Yi-Lin Sophia
Potential Therapeutic Role of Hispidulin in Gastric Cancer through Induction of Apoptosis via NAG-1 Signaling
title Potential Therapeutic Role of Hispidulin in Gastric Cancer through Induction of Apoptosis via NAG-1 Signaling
title_full Potential Therapeutic Role of Hispidulin in Gastric Cancer through Induction of Apoptosis via NAG-1 Signaling
title_fullStr Potential Therapeutic Role of Hispidulin in Gastric Cancer through Induction of Apoptosis via NAG-1 Signaling
title_full_unstemmed Potential Therapeutic Role of Hispidulin in Gastric Cancer through Induction of Apoptosis via NAG-1 Signaling
title_short Potential Therapeutic Role of Hispidulin in Gastric Cancer through Induction of Apoptosis via NAG-1 Signaling
title_sort potential therapeutic role of hispidulin in gastric cancer through induction of apoptosis via nag-1 signaling
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3789485/
https://www.ncbi.nlm.nih.gov/pubmed/24159347
http://dx.doi.org/10.1155/2013/518301
work_keys_str_mv AT yuchaoyuan potentialtherapeuticroleofhispiduliningastriccancerthroughinductionofapoptosisvianag1signaling
AT sukangyi potentialtherapeuticroleofhispiduliningastriccancerthroughinductionofapoptosisvianag1signaling
AT leepolei potentialtherapeuticroleofhispiduliningastriccancerthroughinductionofapoptosisvianag1signaling
AT jhanjieyu potentialtherapeuticroleofhispiduliningastriccancerthroughinductionofapoptosisvianag1signaling
AT tsaopohung potentialtherapeuticroleofhispiduliningastriccancerthroughinductionofapoptosisvianag1signaling
AT chandechuan potentialtherapeuticroleofhispiduliningastriccancerthroughinductionofapoptosisvianag1signaling
AT chenyilinsophia potentialtherapeuticroleofhispiduliningastriccancerthroughinductionofapoptosisvianag1signaling