In Vivo Anti-Cancer Mechanism of Low-Molecular-Weight Fucosylated Chondroitin Sulfate (LFCS) from Sea Cucumber Cucumaria frondosa

The low-molecular-weight fucosylated chondroitin sulfate (LFCS) was prepared from native fucosylated chondroitin sulfate (FCS), which was extracted and isolated from sea cucumber Cucumaria frondosa, and the anti-cancer mechanism of LFCS on mouse Lewis lung carcinoma (LLC) was investigated. The resul...

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Published in:Molecules
Main Authors: Xiaoxiao Liu, Yong Liu, Jiejie Hao, Xiaoliang Zhao, Yinzhi Lang, Fei Fan, Chao Cai, Guoyun Li, Lijuan Zhang, Guangli Yu
Format: Article in Journal/Newspaper
Language:English
Published: MDPI AG 2016
Subjects:
Online Access:https://doi.org/10.3390/molecules21050625
https://doaj.org/article/0d7964b0f549449faff0f0d74f46a5d7
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spelling ftdoajarticles:oai:doaj.org/article:0d7964b0f549449faff0f0d74f46a5d7 2023-05-15T15:59:37+02:00 In Vivo Anti-Cancer Mechanism of Low-Molecular-Weight Fucosylated Chondroitin Sulfate (LFCS) from Sea Cucumber Cucumaria frondosa Xiaoxiao Liu Yong Liu Jiejie Hao Xiaoliang Zhao Yinzhi Lang Fei Fan Chao Cai Guoyun Li Lijuan Zhang Guangli Yu 2016-05-01T00:00:00Z https://doi.org/10.3390/molecules21050625 https://doaj.org/article/0d7964b0f549449faff0f0d74f46a5d7 EN eng MDPI AG http://www.mdpi.com/1420-3049/21/5/625 https://doaj.org/toc/1420-3049 1420-3049 doi:10.3390/molecules21050625 https://doaj.org/article/0d7964b0f549449faff0f0d74f46a5d7 Molecules, Vol 21, Iss 5, p 625 (2016) low-molecular-weight fucosylated chondroitin sulfate anti-metastasis anti-angiogenesis Lewis lung carcinoma mechanism NF-κB Organic chemistry QD241-441 article 2016 ftdoajarticles https://doi.org/10.3390/molecules21050625 2022-12-31T01:57:02Z The low-molecular-weight fucosylated chondroitin sulfate (LFCS) was prepared from native fucosylated chondroitin sulfate (FCS), which was extracted and isolated from sea cucumber Cucumaria frondosa, and the anti-cancer mechanism of LFCS on mouse Lewis lung carcinoma (LLC) was investigated. The results showed that LFCS remarkably inhibited LLC growth and metastasis in a dose-dependent manner. LFCS induced cell cycle arrest by increasing p53/p21 expression and apoptosis through activation of caspase-3 activity in LLC cells. Meanwhile, LFCS suppressed the expression of vascular endothelial growth factor (VEGF), increased the expression of tissue inhibitor of metalloproteinase-1 (TIMP-1) and downregulated the matrix metalloproteinases (MMPs) level. Furthermore, LFCS significantly suppressed the activation of ERK1/2/p38 MAPK/NF-κB pathway, which played a prime role in expression of MMPs. All of these data indicate LFCS may be used as anti-cancer drug candidates and deserve further study. Article in Journal/Newspaper Cucumaria frondosa Directory of Open Access Journals: DOAJ Articles Molecules 21 5 625
institution Open Polar
collection Directory of Open Access Journals: DOAJ Articles
op_collection_id ftdoajarticles
language English
topic low-molecular-weight fucosylated chondroitin sulfate
anti-metastasis
anti-angiogenesis
Lewis lung carcinoma
mechanism
NF-κB
Organic chemistry
QD241-441
spellingShingle low-molecular-weight fucosylated chondroitin sulfate
anti-metastasis
anti-angiogenesis
Lewis lung carcinoma
mechanism
NF-κB
Organic chemistry
QD241-441
Xiaoxiao Liu
Yong Liu
Jiejie Hao
Xiaoliang Zhao
Yinzhi Lang
Fei Fan
Chao Cai
Guoyun Li
Lijuan Zhang
Guangli Yu
In Vivo Anti-Cancer Mechanism of Low-Molecular-Weight Fucosylated Chondroitin Sulfate (LFCS) from Sea Cucumber Cucumaria frondosa
topic_facet low-molecular-weight fucosylated chondroitin sulfate
anti-metastasis
anti-angiogenesis
Lewis lung carcinoma
mechanism
NF-κB
Organic chemistry
QD241-441
description The low-molecular-weight fucosylated chondroitin sulfate (LFCS) was prepared from native fucosylated chondroitin sulfate (FCS), which was extracted and isolated from sea cucumber Cucumaria frondosa, and the anti-cancer mechanism of LFCS on mouse Lewis lung carcinoma (LLC) was investigated. The results showed that LFCS remarkably inhibited LLC growth and metastasis in a dose-dependent manner. LFCS induced cell cycle arrest by increasing p53/p21 expression and apoptosis through activation of caspase-3 activity in LLC cells. Meanwhile, LFCS suppressed the expression of vascular endothelial growth factor (VEGF), increased the expression of tissue inhibitor of metalloproteinase-1 (TIMP-1) and downregulated the matrix metalloproteinases (MMPs) level. Furthermore, LFCS significantly suppressed the activation of ERK1/2/p38 MAPK/NF-κB pathway, which played a prime role in expression of MMPs. All of these data indicate LFCS may be used as anti-cancer drug candidates and deserve further study.
format Article in Journal/Newspaper
author Xiaoxiao Liu
Yong Liu
Jiejie Hao
Xiaoliang Zhao
Yinzhi Lang
Fei Fan
Chao Cai
Guoyun Li
Lijuan Zhang
Guangli Yu
author_facet Xiaoxiao Liu
Yong Liu
Jiejie Hao
Xiaoliang Zhao
Yinzhi Lang
Fei Fan
Chao Cai
Guoyun Li
Lijuan Zhang
Guangli Yu
author_sort Xiaoxiao Liu
title In Vivo Anti-Cancer Mechanism of Low-Molecular-Weight Fucosylated Chondroitin Sulfate (LFCS) from Sea Cucumber Cucumaria frondosa
title_short In Vivo Anti-Cancer Mechanism of Low-Molecular-Weight Fucosylated Chondroitin Sulfate (LFCS) from Sea Cucumber Cucumaria frondosa
title_full In Vivo Anti-Cancer Mechanism of Low-Molecular-Weight Fucosylated Chondroitin Sulfate (LFCS) from Sea Cucumber Cucumaria frondosa
title_fullStr In Vivo Anti-Cancer Mechanism of Low-Molecular-Weight Fucosylated Chondroitin Sulfate (LFCS) from Sea Cucumber Cucumaria frondosa
title_full_unstemmed In Vivo Anti-Cancer Mechanism of Low-Molecular-Weight Fucosylated Chondroitin Sulfate (LFCS) from Sea Cucumber Cucumaria frondosa
title_sort in vivo anti-cancer mechanism of low-molecular-weight fucosylated chondroitin sulfate (lfcs) from sea cucumber cucumaria frondosa
publisher MDPI AG
publishDate 2016
url https://doi.org/10.3390/molecules21050625
https://doaj.org/article/0d7964b0f549449faff0f0d74f46a5d7
genre Cucumaria frondosa
genre_facet Cucumaria frondosa
op_source Molecules, Vol 21, Iss 5, p 625 (2016)
op_relation http://www.mdpi.com/1420-3049/21/5/625
https://doaj.org/toc/1420-3049
1420-3049
doi:10.3390/molecules21050625
https://doaj.org/article/0d7964b0f549449faff0f0d74f46a5d7
op_doi https://doi.org/10.3390/molecules21050625
container_title Molecules
container_volume 21
container_issue 5
container_start_page 625
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