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The Methanol Extract of Angelica sinensis Induces Cell Apoptosis and Suppresses Tumor Growth in Human Malignant Brain Tumors
Glioblastoma multiforme (GBM) is a highly vascularized and invasive neoplasm. The methanol extract of Angelica sinensis (AS-M) is commonly used in traditional Chinese medicine to treat several diseases, such as gastric mucosal damage, hepatic injury, menopausal symptoms, and chronic glomerulonephrit...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3844186/ https://www.ncbi.nlm.nih.gov/pubmed/24319475 http://dx.doi.org/10.1155/2013/394636 |
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author | Lin, Yu-Ling Lai, Wen-Lin Harn, Horng-jyh Hung, Pei-Hsiu Hsieh, Ming-Chang Chang, Kai-Fu Huang, Xiao-Fan Liao, Kuang-Wen Lee, Ming-Shih Tsai, Nu-Man |
author_facet | Lin, Yu-Ling Lai, Wen-Lin Harn, Horng-jyh Hung, Pei-Hsiu Hsieh, Ming-Chang Chang, Kai-Fu Huang, Xiao-Fan Liao, Kuang-Wen Lee, Ming-Shih Tsai, Nu-Man |
author_sort | Lin, Yu-Ling |
collection | PubMed |
description | Glioblastoma multiforme (GBM) is a highly vascularized and invasive neoplasm. The methanol extract of Angelica sinensis (AS-M) is commonly used in traditional Chinese medicine to treat several diseases, such as gastric mucosal damage, hepatic injury, menopausal symptoms, and chronic glomerulonephritis. AS-M also displays potency in suppressing the growth of malignant brain tumor cells. The growth suppression of malignant brain tumor cells by AS-M results from cell cycle arrest and apoptosis. AS-M upregulates expression of cyclin kinase inhibitors, including p16, to decrease the phosphorylation of Rb proteins, resulting in arrest at the G(0)-G(1) phase. The expression of the p53 protein is increased by AS-M and correlates with activation of apoptosis-associated proteins. Therefore, the apoptosis of cancer cells induced by AS-M may be triggered through the p53 pathway. In in vivo studies, AS-M not only suppresses the growth of human malignant brain tumors but also significantly prolongs patient survival. In addition, AS-M has potent anticancer effects involving cell cycle arrest, apoptosis, and antiangiogenesis. The in vitro and in vivo anticancer effects of AS-M indicate that this extract warrants further investigation and potential development as a new antibrain tumor agent, providing new hope for the chemotherapy of malignant brain cancer. |
format | Online Article Text |
id | pubmed-3844186 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-38441862013-12-08 The Methanol Extract of Angelica sinensis Induces Cell Apoptosis and Suppresses Tumor Growth in Human Malignant Brain Tumors Lin, Yu-Ling Lai, Wen-Lin Harn, Horng-jyh Hung, Pei-Hsiu Hsieh, Ming-Chang Chang, Kai-Fu Huang, Xiao-Fan Liao, Kuang-Wen Lee, Ming-Shih Tsai, Nu-Man Evid Based Complement Alternat Med Research Article Glioblastoma multiforme (GBM) is a highly vascularized and invasive neoplasm. The methanol extract of Angelica sinensis (AS-M) is commonly used in traditional Chinese medicine to treat several diseases, such as gastric mucosal damage, hepatic injury, menopausal symptoms, and chronic glomerulonephritis. AS-M also displays potency in suppressing the growth of malignant brain tumor cells. The growth suppression of malignant brain tumor cells by AS-M results from cell cycle arrest and apoptosis. AS-M upregulates expression of cyclin kinase inhibitors, including p16, to decrease the phosphorylation of Rb proteins, resulting in arrest at the G(0)-G(1) phase. The expression of the p53 protein is increased by AS-M and correlates with activation of apoptosis-associated proteins. Therefore, the apoptosis of cancer cells induced by AS-M may be triggered through the p53 pathway. In in vivo studies, AS-M not only suppresses the growth of human malignant brain tumors but also significantly prolongs patient survival. In addition, AS-M has potent anticancer effects involving cell cycle arrest, apoptosis, and antiangiogenesis. The in vitro and in vivo anticancer effects of AS-M indicate that this extract warrants further investigation and potential development as a new antibrain tumor agent, providing new hope for the chemotherapy of malignant brain cancer. Hindawi Publishing Corporation 2013 2013-11-10 /pmc/articles/PMC3844186/ /pubmed/24319475 http://dx.doi.org/10.1155/2013/394636 Text en Copyright © 2013 Yu-Ling Lin et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Lin, Yu-Ling Lai, Wen-Lin Harn, Horng-jyh Hung, Pei-Hsiu Hsieh, Ming-Chang Chang, Kai-Fu Huang, Xiao-Fan Liao, Kuang-Wen Lee, Ming-Shih Tsai, Nu-Man The Methanol Extract of Angelica sinensis Induces Cell Apoptosis and Suppresses Tumor Growth in Human Malignant Brain Tumors |
title | The Methanol Extract of Angelica sinensis Induces Cell Apoptosis and Suppresses Tumor Growth in Human Malignant Brain Tumors |
title_full | The Methanol Extract of Angelica sinensis Induces Cell Apoptosis and Suppresses Tumor Growth in Human Malignant Brain Tumors |
title_fullStr | The Methanol Extract of Angelica sinensis Induces Cell Apoptosis and Suppresses Tumor Growth in Human Malignant Brain Tumors |
title_full_unstemmed | The Methanol Extract of Angelica sinensis Induces Cell Apoptosis and Suppresses Tumor Growth in Human Malignant Brain Tumors |
title_short | The Methanol Extract of Angelica sinensis Induces Cell Apoptosis and Suppresses Tumor Growth in Human Malignant Brain Tumors |
title_sort | methanol extract of angelica sinensis induces cell apoptosis and suppresses tumor growth in human malignant brain tumors |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3844186/ https://www.ncbi.nlm.nih.gov/pubmed/24319475 http://dx.doi.org/10.1155/2013/394636 |
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