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Two Molecular Weights Holothurian Glycosaminoglycan and Hematoporphyrin Derivative-Photodynamic Therapy Inhibit Proliferation and Promote Apoptosis of Human Lung Adenocarcinoma Cells
Holothurian glycosaminoglycan (hGAG) is extracted from the body wall of the sea cucumber, and previous studies have shown many unique bioactivities of hGAG, including antitumor, anti-angiogenesis, anti coagulation, anti thrombosis, anti-inflammation, antidiabetic effect, antivirus, and immune regula...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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SAGE Publications
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9834781/ https://www.ncbi.nlm.nih.gov/pubmed/36624619 http://dx.doi.org/10.1177/15347354221144310 |
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author | Hao-Yu, Dai Ding-Yi, Yu Bao-Hong, Xiao Aihua, Sui Xiao-Qian, Ding Cun-Zhi, Lin |
author_facet | Hao-Yu, Dai Ding-Yi, Yu Bao-Hong, Xiao Aihua, Sui Xiao-Qian, Ding Cun-Zhi, Lin |
author_sort | Hao-Yu, Dai |
collection | PubMed |
description | Holothurian glycosaminoglycan (hGAG) is extracted from the body wall of the sea cucumber, and previous studies have shown many unique bioactivities of hGAG, including antitumor, anti-angiogenesis, anti coagulation, anti thrombosis, anti-inflammation, antidiabetic effect, antivirus, and immune regulation. The effects of 3W and 5W molecular weights hGAG with hematoporphyrin derivative-photodynamic therapy (HPD-PDT) on lung cancer were investigated. Human lung adenocarcinoma A549 cells were divided into 6 groups: control group, 3W molecular weight hGAG group, 5W molecular weight hGAG group, HPD-PDT group, 3W molecular weight hGAG + HPD-PDT group, and 5W molecular weight hGAG + HPD-PDT group. Cell morphology was observed under inverted phase contrast microscope. Cell proliferative activity was detected by CCK8 and cell apoptosis was assayed by Hoechst33258 staining and flow cytometry. The results showed that two different molecular weights hGAG could inhibit proliferation, promote apoptosis rates of A549 cells, and enhance the sensitivity of A549 cells to HPD-PDT. The combined use of hGAG and HPD-PDT has synergistic inhibitory effects on A549 cells, and the effects of 3W molecular weight hGAG are better than that of 5W molecular weight hGAG. |
format | Online Article Text |
id | pubmed-9834781 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-98347812023-01-13 Two Molecular Weights Holothurian Glycosaminoglycan and Hematoporphyrin Derivative-Photodynamic Therapy Inhibit Proliferation and Promote Apoptosis of Human Lung Adenocarcinoma Cells Hao-Yu, Dai Ding-Yi, Yu Bao-Hong, Xiao Aihua, Sui Xiao-Qian, Ding Cun-Zhi, Lin Integr Cancer Ther Research Article Holothurian glycosaminoglycan (hGAG) is extracted from the body wall of the sea cucumber, and previous studies have shown many unique bioactivities of hGAG, including antitumor, anti-angiogenesis, anti coagulation, anti thrombosis, anti-inflammation, antidiabetic effect, antivirus, and immune regulation. The effects of 3W and 5W molecular weights hGAG with hematoporphyrin derivative-photodynamic therapy (HPD-PDT) on lung cancer were investigated. Human lung adenocarcinoma A549 cells were divided into 6 groups: control group, 3W molecular weight hGAG group, 5W molecular weight hGAG group, HPD-PDT group, 3W molecular weight hGAG + HPD-PDT group, and 5W molecular weight hGAG + HPD-PDT group. Cell morphology was observed under inverted phase contrast microscope. Cell proliferative activity was detected by CCK8 and cell apoptosis was assayed by Hoechst33258 staining and flow cytometry. The results showed that two different molecular weights hGAG could inhibit proliferation, promote apoptosis rates of A549 cells, and enhance the sensitivity of A549 cells to HPD-PDT. The combined use of hGAG and HPD-PDT has synergistic inhibitory effects on A549 cells, and the effects of 3W molecular weight hGAG are better than that of 5W molecular weight hGAG. SAGE Publications 2023-01-09 /pmc/articles/PMC9834781/ /pubmed/36624619 http://dx.doi.org/10.1177/15347354221144310 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Research Article Hao-Yu, Dai Ding-Yi, Yu Bao-Hong, Xiao Aihua, Sui Xiao-Qian, Ding Cun-Zhi, Lin Two Molecular Weights Holothurian Glycosaminoglycan and Hematoporphyrin Derivative-Photodynamic Therapy Inhibit Proliferation and Promote Apoptosis of Human Lung Adenocarcinoma Cells |
title | Two Molecular Weights Holothurian Glycosaminoglycan and
Hematoporphyrin Derivative-Photodynamic Therapy Inhibit Proliferation and
Promote Apoptosis of Human Lung Adenocarcinoma Cells |
title_full | Two Molecular Weights Holothurian Glycosaminoglycan and
Hematoporphyrin Derivative-Photodynamic Therapy Inhibit Proliferation and
Promote Apoptosis of Human Lung Adenocarcinoma Cells |
title_fullStr | Two Molecular Weights Holothurian Glycosaminoglycan and
Hematoporphyrin Derivative-Photodynamic Therapy Inhibit Proliferation and
Promote Apoptosis of Human Lung Adenocarcinoma Cells |
title_full_unstemmed | Two Molecular Weights Holothurian Glycosaminoglycan and
Hematoporphyrin Derivative-Photodynamic Therapy Inhibit Proliferation and
Promote Apoptosis of Human Lung Adenocarcinoma Cells |
title_short | Two Molecular Weights Holothurian Glycosaminoglycan and
Hematoporphyrin Derivative-Photodynamic Therapy Inhibit Proliferation and
Promote Apoptosis of Human Lung Adenocarcinoma Cells |
title_sort | two molecular weights holothurian glycosaminoglycan and
hematoporphyrin derivative-photodynamic therapy inhibit proliferation and
promote apoptosis of human lung adenocarcinoma cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9834781/ https://www.ncbi.nlm.nih.gov/pubmed/36624619 http://dx.doi.org/10.1177/15347354221144310 |
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