Study on the Putative Structure and the Biological Functions of Fucoidan

碩士 === 國立陽明大學 === 醫學生物技術暨檢驗學系 === 102 === Fucoidan, a water-soluble and sulfated-fucans having complicated chemical structures, commonly found in brown seaweeds. Our previous studies demonstrated that fucoidan inhibits the growth of lung cancer cells and breast cancer cells. Here, we focus on the re...

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Main Authors: Mi-Hsuan Lin, 林宓璇
Other Authors: Hsien-Yeh Hsu
Format: Others
Language:en_US
Published: 2014
Online Access:http://ndltd.ncl.edu.tw/handle/59245635011318004556
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spelling ndltd-TW-102YM0056040092015-10-13T23:50:22Z http://ndltd.ncl.edu.tw/handle/59245635011318004556 Study on the Putative Structure and the Biological Functions of Fucoidan 研究褐藻醣膠中特定結構之生物活性 Mi-Hsuan Lin 林宓璇 碩士 國立陽明大學 醫學生物技術暨檢驗學系 102 Fucoidan, a water-soluble and sulfated-fucans having complicated chemical structures, commonly found in brown seaweeds. Our previous studies demonstrated that fucoidan inhibits the growth of lung cancer cells and breast cancer cells. Here, we focus on the relationship between its chemical composition and in vitro anticancer activity. The major low molecular mass of fucoidan is named LMF and estimated average molecular mass about 500 Da by size-exclusion high-performance liquid chromatography (SEC-HPLC). To examine the content of fucose of LMF, we hydrolyzed the LMF via autoclave (121℃) and acetic acid. The residue was further applied the high-performance anion exchange chromatography (HPAEC) to identify the content of fucose from hydrolyzed LMF. We found that the released fucose from LMF was increased with a time-dependent manner by autoclave or a does-dependent of acetic acid in autoclave. Next, we examined the anti-cancer activity of the hydrolyzed LMF. Our previous studies demonstrated that fucoidan enhances transforming growth factor β (TGFβ) and its receptors (TGFRs) degradation in cancer cells. Here we found that LMF enhanced TGFRs degradation, whereas, the hydrolyzed LMF did not affect expression of TGFRs and decrease the viability of cancer cells. Furthermore, we examined the components of LMF by electrospray ionization mass spectrometry (ESI/MS), we found that the sulfated fucose group presented on the LMF. The results showed an essential factor in this study, the hydrolyzed LMF lost the sulfated group from fucose that the higher content of sulfated fucose group of LMF (SO3-LMF) induced the expression of LC3-II (an autophagy marker), but not hydrolyzed LMF. Taken together, we proposed that the bioactivity of fucoidan may be contributed from the content of sulfated fucose group on low molecular mass fucoidan. Hsien-Yeh Hsu Wen-Bin Yang 許先業 楊文彬 2014 學位論文 ; thesis 36 en_US
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description 碩士 === 國立陽明大學 === 醫學生物技術暨檢驗學系 === 102 === Fucoidan, a water-soluble and sulfated-fucans having complicated chemical structures, commonly found in brown seaweeds. Our previous studies demonstrated that fucoidan inhibits the growth of lung cancer cells and breast cancer cells. Here, we focus on the relationship between its chemical composition and in vitro anticancer activity. The major low molecular mass of fucoidan is named LMF and estimated average molecular mass about 500 Da by size-exclusion high-performance liquid chromatography (SEC-HPLC). To examine the content of fucose of LMF, we hydrolyzed the LMF via autoclave (121℃) and acetic acid. The residue was further applied the high-performance anion exchange chromatography (HPAEC) to identify the content of fucose from hydrolyzed LMF. We found that the released fucose from LMF was increased with a time-dependent manner by autoclave or a does-dependent of acetic acid in autoclave. Next, we examined the anti-cancer activity of the hydrolyzed LMF. Our previous studies demonstrated that fucoidan enhances transforming growth factor β (TGFβ) and its receptors (TGFRs) degradation in cancer cells. Here we found that LMF enhanced TGFRs degradation, whereas, the hydrolyzed LMF did not affect expression of TGFRs and decrease the viability of cancer cells. Furthermore, we examined the components of LMF by electrospray ionization mass spectrometry (ESI/MS), we found that the sulfated fucose group presented on the LMF. The results showed an essential factor in this study, the hydrolyzed LMF lost the sulfated group from fucose that the higher content of sulfated fucose group of LMF (SO3-LMF) induced the expression of LC3-II (an autophagy marker), but not hydrolyzed LMF. Taken together, we proposed that the bioactivity of fucoidan may be contributed from the content of sulfated fucose group on low molecular mass fucoidan.
author2 Hsien-Yeh Hsu
author_facet Hsien-Yeh Hsu
Mi-Hsuan Lin
林宓璇
author Mi-Hsuan Lin
林宓璇
spellingShingle Mi-Hsuan Lin
林宓璇
Study on the Putative Structure and the Biological Functions of Fucoidan
author_sort Mi-Hsuan Lin
title Study on the Putative Structure and the Biological Functions of Fucoidan
title_short Study on the Putative Structure and the Biological Functions of Fucoidan
title_full Study on the Putative Structure and the Biological Functions of Fucoidan
title_fullStr Study on the Putative Structure and the Biological Functions of Fucoidan
title_full_unstemmed Study on the Putative Structure and the Biological Functions of Fucoidan
title_sort study on the putative structure and the biological functions of fucoidan
publishDate 2014
url http://ndltd.ncl.edu.tw/handle/59245635011318004556
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