Cytotoxic and Apoptosis-Inducing Activity of Triterpene Glycosides from Holothuria scabra and Cucumaria frondosa against HepG2 Cells

The cytotoxic effects of thirteen triterpene glycosides from Holothuria scabra Jaeger and Cucumaria frondosa Gunnerus (Holothuroidea) against four human cell lines were detected and their cytotoxicity-structure relationships were established. The apoptosis-inducing activity of a more potent glycosid...

Full description

Bibliographic Details
Published in:Marine Drugs
Main Authors: Juanjuan Wang, Hua Han, Xiangfeng Chen, Yanghua Yi, Hongxiang Sun
Format: Text
Language:English
Published: Multidisciplinary Digital Publishing Institute 2014
Subjects:
Online Access:https://doi.org/10.3390/md12084274
id ftmdpi:oai:mdpi.com:/1660-3397/12/8/4274/
record_format openpolar
spelling ftmdpi:oai:mdpi.com:/1660-3397/12/8/4274/ 2023-08-20T04:06:06+02:00 Cytotoxic and Apoptosis-Inducing Activity of Triterpene Glycosides from Holothuria scabra and Cucumaria frondosa against HepG2 Cells Juanjuan Wang Hua Han Xiangfeng Chen Yanghua Yi Hongxiang Sun agris 2014-07-24 application/pdf https://doi.org/10.3390/md12084274 EN eng Multidisciplinary Digital Publishing Institute https://dx.doi.org/10.3390/md12084274 https://creativecommons.org/licenses/by/3.0/ Marine Drugs; Volume 12; Issue 8; Pages: 4274-4290 Holothuria scabra Cucumaria frondosa triterpene glycosides echinoside A cytotoxicity structure-activity relationship apoptosis mechanism Text 2014 ftmdpi https://doi.org/10.3390/md12084274 2023-07-31T20:38:28Z The cytotoxic effects of thirteen triterpene glycosides from Holothuria scabra Jaeger and Cucumaria frondosa Gunnerus (Holothuroidea) against four human cell lines were detected and their cytotoxicity-structure relationships were established. The apoptosis-inducing activity of a more potent glycoside echinoside A (1) in HepG2 cells was further investigated by determining its effect on the morphology, mitochondrial transmembrane potential (Δψm) and mRNA expression levels of the apoptosis-related genes. The results showed that the number of glycosyl residues in sugar chains and the side chain of aglycone could affect their cytotoxicity towards tumor cells and selective cytotoxicity. 1 significantly inhibited cell viability and induced apoptosis in HepG2 cells. 1 also markedly decreased the Δψm and Bcl-2/Bax mRNA express ratio, and up-regulated the mRNA expression levels of Caspase-3, Caspase-8 and Caspase-9 in HepG2 cells. Therefore, 1 induced apoptosis in HepG2 cells through both intrinsic and extrinsic pathway. These findings could potentially promote the usage of these glycosides as leading compounds for developing new antitumor drugs. Text Cucumaria frondosa MDPI Open Access Publishing Marine Drugs 12 8 4274 4290
institution Open Polar
collection MDPI Open Access Publishing
op_collection_id ftmdpi
language English
topic Holothuria scabra
Cucumaria frondosa
triterpene glycosides
echinoside A
cytotoxicity
structure-activity relationship
apoptosis
mechanism
spellingShingle Holothuria scabra
Cucumaria frondosa
triterpene glycosides
echinoside A
cytotoxicity
structure-activity relationship
apoptosis
mechanism
Juanjuan Wang
Hua Han
Xiangfeng Chen
Yanghua Yi
Hongxiang Sun
Cytotoxic and Apoptosis-Inducing Activity of Triterpene Glycosides from Holothuria scabra and Cucumaria frondosa against HepG2 Cells
topic_facet Holothuria scabra
Cucumaria frondosa
triterpene glycosides
echinoside A
cytotoxicity
structure-activity relationship
apoptosis
mechanism
description The cytotoxic effects of thirteen triterpene glycosides from Holothuria scabra Jaeger and Cucumaria frondosa Gunnerus (Holothuroidea) against four human cell lines were detected and their cytotoxicity-structure relationships were established. The apoptosis-inducing activity of a more potent glycoside echinoside A (1) in HepG2 cells was further investigated by determining its effect on the morphology, mitochondrial transmembrane potential (Δψm) and mRNA expression levels of the apoptosis-related genes. The results showed that the number of glycosyl residues in sugar chains and the side chain of aglycone could affect their cytotoxicity towards tumor cells and selective cytotoxicity. 1 significantly inhibited cell viability and induced apoptosis in HepG2 cells. 1 also markedly decreased the Δψm and Bcl-2/Bax mRNA express ratio, and up-regulated the mRNA expression levels of Caspase-3, Caspase-8 and Caspase-9 in HepG2 cells. Therefore, 1 induced apoptosis in HepG2 cells through both intrinsic and extrinsic pathway. These findings could potentially promote the usage of these glycosides as leading compounds for developing new antitumor drugs.
format Text
author Juanjuan Wang
Hua Han
Xiangfeng Chen
Yanghua Yi
Hongxiang Sun
author_facet Juanjuan Wang
Hua Han
Xiangfeng Chen
Yanghua Yi
Hongxiang Sun
author_sort Juanjuan Wang
title Cytotoxic and Apoptosis-Inducing Activity of Triterpene Glycosides from Holothuria scabra and Cucumaria frondosa against HepG2 Cells
title_short Cytotoxic and Apoptosis-Inducing Activity of Triterpene Glycosides from Holothuria scabra and Cucumaria frondosa against HepG2 Cells
title_full Cytotoxic and Apoptosis-Inducing Activity of Triterpene Glycosides from Holothuria scabra and Cucumaria frondosa against HepG2 Cells
title_fullStr Cytotoxic and Apoptosis-Inducing Activity of Triterpene Glycosides from Holothuria scabra and Cucumaria frondosa against HepG2 Cells
title_full_unstemmed Cytotoxic and Apoptosis-Inducing Activity of Triterpene Glycosides from Holothuria scabra and Cucumaria frondosa against HepG2 Cells
title_sort cytotoxic and apoptosis-inducing activity of triterpene glycosides from holothuria scabra and cucumaria frondosa against hepg2 cells
publisher Multidisciplinary Digital Publishing Institute
publishDate 2014
url https://doi.org/10.3390/md12084274
op_coverage agris
genre Cucumaria frondosa
genre_facet Cucumaria frondosa
op_source Marine Drugs; Volume 12; Issue 8; Pages: 4274-4290
op_relation https://dx.doi.org/10.3390/md12084274
op_rights https://creativecommons.org/licenses/by/3.0/
op_doi https://doi.org/10.3390/md12084274
container_title Marine Drugs
container_volume 12
container_issue 8
container_start_page 4274
op_container_end_page 4290
_version_ 1774717018123010048