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A Novel, Stable, Estradiol-Stimulating, Osteogenic Yam Protein with Potential for the Treatment of Menopausal Syndrome
A novel protein, designated as DOI, isolated from the Chinese yam (Dioscorea opposita Thunb.) could be the first protein drug for the treatment of menopausal syndrome and an alternative to hormone replacement therapy (HRT), which is known to have undesirable side effects. DOI is an acid- and thermo-...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5155516/ https://www.ncbi.nlm.nih.gov/pubmed/26160710 http://dx.doi.org/10.1038/srep10179 |
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author | Lok Wong, Kam Ming Lai, Yau Li, Ka Wan Fai Lee, Kai Ng, Tzi Bun Pan Cheung, Ho Bo Zhang, Yan Lao, Lixing Ngok-Shun Wong, Ricky Chui Shaw, Pang Ho Wong, Jack Zhang, Zhang-Jin Lam, Jenny Ka Wing Wencai, YE Wing Sze, Stephen Cho |
author_facet | Lok Wong, Kam Ming Lai, Yau Li, Ka Wan Fai Lee, Kai Ng, Tzi Bun Pan Cheung, Ho Bo Zhang, Yan Lao, Lixing Ngok-Shun Wong, Ricky Chui Shaw, Pang Ho Wong, Jack Zhang, Zhang-Jin Lam, Jenny Ka Wing Wencai, YE Wing Sze, Stephen Cho |
author_sort | Lok Wong, Kam |
collection | PubMed |
description | A novel protein, designated as DOI, isolated from the Chinese yam (Dioscorea opposita Thunb.) could be the first protein drug for the treatment of menopausal syndrome and an alternative to hormone replacement therapy (HRT), which is known to have undesirable side effects. DOI is an acid- and thermo-stable protein with a distinctive N-terminal sequence Gly-Ile-Gly-Lys-Ile-Thr-Thr-Tyr-Trp-Gly-Gln-Tyr-Ser-Asp-Glu-Pro-Ser-Leu-Thr-Glu. DOI was found to stimulate estradiol biosynthesis in rat ovarian granulosa cells; induce estradiol and progesterone secretion in 16- to 18-month-old female Sprague Dawley rats by upregulating expressions of follicle-stimulating hormone receptor and ovarian aromatase; counteract the progression of osteoporosis and augment bone mineral density; and improve cognitive functioning by upregulating protein expressions of brain-derived neurotrophic factor and TrkB receptors in the prefrontal cortex. Furthermore, DOI did not stimulate the proliferation of breast cancer and ovarian cancer cells, which suggest it could be a more efficacious and safer alternative to HRT. |
format | Online Article Text |
id | pubmed-5155516 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-51555162016-12-20 A Novel, Stable, Estradiol-Stimulating, Osteogenic Yam Protein with Potential for the Treatment of Menopausal Syndrome Lok Wong, Kam Ming Lai, Yau Li, Ka Wan Fai Lee, Kai Ng, Tzi Bun Pan Cheung, Ho Bo Zhang, Yan Lao, Lixing Ngok-Shun Wong, Ricky Chui Shaw, Pang Ho Wong, Jack Zhang, Zhang-Jin Lam, Jenny Ka Wing Wencai, YE Wing Sze, Stephen Cho Sci Rep Article A novel protein, designated as DOI, isolated from the Chinese yam (Dioscorea opposita Thunb.) could be the first protein drug for the treatment of menopausal syndrome and an alternative to hormone replacement therapy (HRT), which is known to have undesirable side effects. DOI is an acid- and thermo-stable protein with a distinctive N-terminal sequence Gly-Ile-Gly-Lys-Ile-Thr-Thr-Tyr-Trp-Gly-Gln-Tyr-Ser-Asp-Glu-Pro-Ser-Leu-Thr-Glu. DOI was found to stimulate estradiol biosynthesis in rat ovarian granulosa cells; induce estradiol and progesterone secretion in 16- to 18-month-old female Sprague Dawley rats by upregulating expressions of follicle-stimulating hormone receptor and ovarian aromatase; counteract the progression of osteoporosis and augment bone mineral density; and improve cognitive functioning by upregulating protein expressions of brain-derived neurotrophic factor and TrkB receptors in the prefrontal cortex. Furthermore, DOI did not stimulate the proliferation of breast cancer and ovarian cancer cells, which suggest it could be a more efficacious and safer alternative to HRT. Nature Publishing Group 2015-07-10 /pmc/articles/PMC5155516/ /pubmed/26160710 http://dx.doi.org/10.1038/srep10179 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Lok Wong, Kam Ming Lai, Yau Li, Ka Wan Fai Lee, Kai Ng, Tzi Bun Pan Cheung, Ho Bo Zhang, Yan Lao, Lixing Ngok-Shun Wong, Ricky Chui Shaw, Pang Ho Wong, Jack Zhang, Zhang-Jin Lam, Jenny Ka Wing Wencai, YE Wing Sze, Stephen Cho A Novel, Stable, Estradiol-Stimulating, Osteogenic Yam Protein with Potential for the Treatment of Menopausal Syndrome |
title | A Novel, Stable, Estradiol-Stimulating, Osteogenic Yam Protein with Potential for the Treatment of Menopausal Syndrome |
title_full | A Novel, Stable, Estradiol-Stimulating, Osteogenic Yam Protein with Potential for the Treatment of Menopausal Syndrome |
title_fullStr | A Novel, Stable, Estradiol-Stimulating, Osteogenic Yam Protein with Potential for the Treatment of Menopausal Syndrome |
title_full_unstemmed | A Novel, Stable, Estradiol-Stimulating, Osteogenic Yam Protein with Potential for the Treatment of Menopausal Syndrome |
title_short | A Novel, Stable, Estradiol-Stimulating, Osteogenic Yam Protein with Potential for the Treatment of Menopausal Syndrome |
title_sort | novel, stable, estradiol-stimulating, osteogenic yam protein with potential for the treatment of menopausal syndrome |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5155516/ https://www.ncbi.nlm.nih.gov/pubmed/26160710 http://dx.doi.org/10.1038/srep10179 |
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