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Tianshengyuan-1 (TSY-1) regulates cellular Telomerase activity by methylation of TERT promoter
Telomere and Telomerase have recently been explored as anti-aging and anti-cancer drug targets with only limited success. Previously we showed that the Chinese herbal medicine Tianshengyuan-1 (TSY-1), an agent used to treat bone marrow deficiency, has a profound effect on stimulating Telomerase acti...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5352375/ https://www.ncbi.nlm.nih.gov/pubmed/28002788 http://dx.doi.org/10.18632/oncotarget.13939 |
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author | Yu, Weibo Qin, Xiaotian Jin, Yusheng Li, Yawei Santiskulvong, Chintda Vu, Victor Zeng, Gang Zhang, Zuofeng Chow, Michelle Rao, Jianyu |
author_facet | Yu, Weibo Qin, Xiaotian Jin, Yusheng Li, Yawei Santiskulvong, Chintda Vu, Victor Zeng, Gang Zhang, Zuofeng Chow, Michelle Rao, Jianyu |
author_sort | Yu, Weibo |
collection | PubMed |
description | Telomere and Telomerase have recently been explored as anti-aging and anti-cancer drug targets with only limited success. Previously we showed that the Chinese herbal medicine Tianshengyuan-1 (TSY-1), an agent used to treat bone marrow deficiency, has a profound effect on stimulating Telomerase activity in hematopoietic cells. Here, the mechanism of TSY-1 on cellular Telomerase activity was further investigated using HL60, a promyelocytic leukemia cell line, normal peripheral blood mononuclear cells, and CD34+ hematopoietic stem cells derived from umbilical cord blood. TSY-1 increases Telomerase activity in normal peripheral blood mononuclear cells and CD34+ hematopoietic stem cells with innately low Telomerase activity but decreases Telomerase activity in HL60 cells with high intrinsic Telomerase activity, both in a dose-response manner. Gene profiling analysis identified Telomerase reverse transcriptase (TERT) as the potential target gene associated with the TSY-1 effect, which was verified by both RT-PCR and western blot analysis. The β-galactosidase reporter staining assay showed that the effect of TSY-1 on Telomerase activity correlates with cell senescence. TSY-1 induced hypomethylation within TERT core promoter in HL60 cells but induced hypermethylation within TERT core promoter in normal peripheral blood mononuclear cells and CD34+ hematopoietic stem cells. TSY-1 appears to affect the Telomerase activity in different cell lines differently and the effect is associated with TERT expression, possibly via the methylation of TERT promoter. |
format | Online Article Text |
id | pubmed-5352375 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-53523752017-04-14 Tianshengyuan-1 (TSY-1) regulates cellular Telomerase activity by methylation of TERT promoter Yu, Weibo Qin, Xiaotian Jin, Yusheng Li, Yawei Santiskulvong, Chintda Vu, Victor Zeng, Gang Zhang, Zuofeng Chow, Michelle Rao, Jianyu Oncotarget Research Paper Telomere and Telomerase have recently been explored as anti-aging and anti-cancer drug targets with only limited success. Previously we showed that the Chinese herbal medicine Tianshengyuan-1 (TSY-1), an agent used to treat bone marrow deficiency, has a profound effect on stimulating Telomerase activity in hematopoietic cells. Here, the mechanism of TSY-1 on cellular Telomerase activity was further investigated using HL60, a promyelocytic leukemia cell line, normal peripheral blood mononuclear cells, and CD34+ hematopoietic stem cells derived from umbilical cord blood. TSY-1 increases Telomerase activity in normal peripheral blood mononuclear cells and CD34+ hematopoietic stem cells with innately low Telomerase activity but decreases Telomerase activity in HL60 cells with high intrinsic Telomerase activity, both in a dose-response manner. Gene profiling analysis identified Telomerase reverse transcriptase (TERT) as the potential target gene associated with the TSY-1 effect, which was verified by both RT-PCR and western blot analysis. The β-galactosidase reporter staining assay showed that the effect of TSY-1 on Telomerase activity correlates with cell senescence. TSY-1 induced hypomethylation within TERT core promoter in HL60 cells but induced hypermethylation within TERT core promoter in normal peripheral blood mononuclear cells and CD34+ hematopoietic stem cells. TSY-1 appears to affect the Telomerase activity in different cell lines differently and the effect is associated with TERT expression, possibly via the methylation of TERT promoter. Impact Journals LLC 2016-12-15 /pmc/articles/PMC5352375/ /pubmed/28002788 http://dx.doi.org/10.18632/oncotarget.13939 Text en Copyright: © 2017 Yu et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Yu, Weibo Qin, Xiaotian Jin, Yusheng Li, Yawei Santiskulvong, Chintda Vu, Victor Zeng, Gang Zhang, Zuofeng Chow, Michelle Rao, Jianyu Tianshengyuan-1 (TSY-1) regulates cellular Telomerase activity by methylation of TERT promoter |
title | Tianshengyuan-1 (TSY-1) regulates cellular Telomerase activity by methylation of TERT promoter |
title_full | Tianshengyuan-1 (TSY-1) regulates cellular Telomerase activity by methylation of TERT promoter |
title_fullStr | Tianshengyuan-1 (TSY-1) regulates cellular Telomerase activity by methylation of TERT promoter |
title_full_unstemmed | Tianshengyuan-1 (TSY-1) regulates cellular Telomerase activity by methylation of TERT promoter |
title_short | Tianshengyuan-1 (TSY-1) regulates cellular Telomerase activity by methylation of TERT promoter |
title_sort | tianshengyuan-1 (tsy-1) regulates cellular telomerase activity by methylation of tert promoter |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5352375/ https://www.ncbi.nlm.nih.gov/pubmed/28002788 http://dx.doi.org/10.18632/oncotarget.13939 |
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