Ginsenosides as anticancer agents: in vitro and in vivo activities, structure-activity relationships, and molecular mechanisms of action

Conventional chemotherapeutic agents are often toxic not only to tumor cells but also to normal cells, limiting their therapeutic use in the clinic. Novel natural product anticancer compounds present an attractive alternative to synthetic compounds, based on their favorable safety and efficacy profi...

Full description

Bibliographic Details
Main Authors: Subhasree Ashok Nag, Jiangjiang eQin, Wei eWang, Ming-Hai eWang, Hui eWang, Ruiwen eZhang
Format: Article
Language:English
Published: Frontiers Media S.A. 2012-02-01
Series:Frontiers in Pharmacology
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fphar.2012.00025/full
_version_ 1819059097162481664
author Subhasree Ashok Nag
Jiangjiang eQin
Wei eWang
Wei eWang
Ming-Hai eWang
Ming-Hai eWang
Hui eWang
Ruiwen eZhang
Ruiwen eZhang
author_facet Subhasree Ashok Nag
Jiangjiang eQin
Wei eWang
Wei eWang
Ming-Hai eWang
Ming-Hai eWang
Hui eWang
Ruiwen eZhang
Ruiwen eZhang
author_sort Subhasree Ashok Nag
collection DOAJ
description Conventional chemotherapeutic agents are often toxic not only to tumor cells but also to normal cells, limiting their therapeutic use in the clinic. Novel natural product anticancer compounds present an attractive alternative to synthetic compounds, based on their favorable safety and efficacy profiles. Several pre-clinical and clinical studies have demonstrated the anticancer potential of Panax ginseng, a widely used traditional Chinese medicine. The anti-tumor efficacy of ginseng is attributed mainly to the presence of saponins, known as ginsenosides. In this review, we focus on how ginsenosides exert their anticancer effects by modulation of diverse signaling pathways, including regulation of cell proliferation mediators (CDKs and cyclins), growth factors (c-myc, EGFR, and VEGF), tumor suppressors (p53 and p21), oncogenes (MDM2), cell death mediators (Bcl-2, Bcl-xL, XIAP, caspases, and death receptors), inflammatory response molecules (NF-κB and COX2), and protein kinases (JNK, Akt, and AMPK). We also discuss the structure-activity relationship (SAR) of various ginsenosides and their potential in the treatment of various human cancers. In summary, recent advances in the discovery and evaluation of ginsenosides as cancer therapeutic agents support further preclinical and clinical development of these agents for the treatment of primary and metastatic tumors.
first_indexed 2024-12-21T14:05:40Z
format Article
id doaj.art-faefeafa0b464fa1a4cfa5dfcea82133
institution Directory Open Access Journal
issn 1663-9812
language English
last_indexed 2024-12-21T14:05:40Z
publishDate 2012-02-01
publisher Frontiers Media S.A.
record_format Article
series Frontiers in Pharmacology
spelling doaj.art-faefeafa0b464fa1a4cfa5dfcea821332022-12-21T19:01:14ZengFrontiers Media S.A.Frontiers in Pharmacology1663-98122012-02-01310.3389/fphar.2012.0002522714Ginsenosides as anticancer agents: in vitro and in vivo activities, structure-activity relationships, and molecular mechanisms of actionSubhasree Ashok Nag0Jiangjiang eQin1Wei eWang2Wei eWang3Ming-Hai eWang4Ming-Hai eWang5Hui eWang6Ruiwen eZhang7Ruiwen eZhang8Texas Tech University Health Sciences CenterTexas Tech University Health Sciences CenterTexas Tech University Health Sciences CenterTexas Tech University Health Sciences CenterTexas Tech University Health Sciences CenterTexas Tech University Health Sciences CenterChinese Academy of SciencesTexas Tech University Health Sciences CenterTexas Tech University Health Sciences CenterConventional chemotherapeutic agents are often toxic not only to tumor cells but also to normal cells, limiting their therapeutic use in the clinic. Novel natural product anticancer compounds present an attractive alternative to synthetic compounds, based on their favorable safety and efficacy profiles. Several pre-clinical and clinical studies have demonstrated the anticancer potential of Panax ginseng, a widely used traditional Chinese medicine. The anti-tumor efficacy of ginseng is attributed mainly to the presence of saponins, known as ginsenosides. In this review, we focus on how ginsenosides exert their anticancer effects by modulation of diverse signaling pathways, including regulation of cell proliferation mediators (CDKs and cyclins), growth factors (c-myc, EGFR, and VEGF), tumor suppressors (p53 and p21), oncogenes (MDM2), cell death mediators (Bcl-2, Bcl-xL, XIAP, caspases, and death receptors), inflammatory response molecules (NF-κB and COX2), and protein kinases (JNK, Akt, and AMPK). We also discuss the structure-activity relationship (SAR) of various ginsenosides and their potential in the treatment of various human cancers. In summary, recent advances in the discovery and evaluation of ginsenosides as cancer therapeutic agents support further preclinical and clinical development of these agents for the treatment of primary and metastatic tumors.http://journal.frontiersin.org/Journal/10.3389/fphar.2012.00025/fullGinsenosidesclinical trialsmolecular mechanismanticancer activitiesPanax genusPanax ginseng
spellingShingle Subhasree Ashok Nag
Jiangjiang eQin
Wei eWang
Wei eWang
Ming-Hai eWang
Ming-Hai eWang
Hui eWang
Ruiwen eZhang
Ruiwen eZhang
Ginsenosides as anticancer agents: in vitro and in vivo activities, structure-activity relationships, and molecular mechanisms of action
Frontiers in Pharmacology
Ginsenosides
clinical trials
molecular mechanism
anticancer activities
Panax genus
Panax ginseng
title Ginsenosides as anticancer agents: in vitro and in vivo activities, structure-activity relationships, and molecular mechanisms of action
title_full Ginsenosides as anticancer agents: in vitro and in vivo activities, structure-activity relationships, and molecular mechanisms of action
title_fullStr Ginsenosides as anticancer agents: in vitro and in vivo activities, structure-activity relationships, and molecular mechanisms of action
title_full_unstemmed Ginsenosides as anticancer agents: in vitro and in vivo activities, structure-activity relationships, and molecular mechanisms of action
title_short Ginsenosides as anticancer agents: in vitro and in vivo activities, structure-activity relationships, and molecular mechanisms of action
title_sort ginsenosides as anticancer agents in vitro and in vivo activities structure activity relationships and molecular mechanisms of action
topic Ginsenosides
clinical trials
molecular mechanism
anticancer activities
Panax genus
Panax ginseng
url http://journal.frontiersin.org/Journal/10.3389/fphar.2012.00025/full
work_keys_str_mv AT subhasreeashoknag ginsenosidesasanticanceragentsinvitroandinvivoactivitiesstructureactivityrelationshipsandmolecularmechanismsofaction
AT jiangjiangeqin ginsenosidesasanticanceragentsinvitroandinvivoactivitiesstructureactivityrelationshipsandmolecularmechanismsofaction
AT weiewang ginsenosidesasanticanceragentsinvitroandinvivoactivitiesstructureactivityrelationshipsandmolecularmechanismsofaction
AT weiewang ginsenosidesasanticanceragentsinvitroandinvivoactivitiesstructureactivityrelationshipsandmolecularmechanismsofaction
AT minghaiewang ginsenosidesasanticanceragentsinvitroandinvivoactivitiesstructureactivityrelationshipsandmolecularmechanismsofaction
AT minghaiewang ginsenosidesasanticanceragentsinvitroandinvivoactivitiesstructureactivityrelationshipsandmolecularmechanismsofaction
AT huiewang ginsenosidesasanticanceragentsinvitroandinvivoactivitiesstructureactivityrelationshipsandmolecularmechanismsofaction
AT ruiwenezhang ginsenosidesasanticanceragentsinvitroandinvivoactivitiesstructureactivityrelationshipsandmolecularmechanismsofaction
AT ruiwenezhang ginsenosidesasanticanceragentsinvitroandinvivoactivitiesstructureactivityrelationshipsandmolecularmechanismsofaction