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Suppressor of Ty 16 promotes lung cancer malignancy and is negatively regulated by miR‐1227‐5p
Suppressor of Ty 16 (Spt16) is a component of the facilitates chromatin transcription (FACT) complex, which is a histone chaperone and involved in gene transcription, DNA replication, and DNA repair. Previous studies showed that FACT is highly expressed in cancer, and cancer cells are more reliant o...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7648015/ https://www.ncbi.nlm.nih.gov/pubmed/32860308 http://dx.doi.org/10.1111/cas.14627 |
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author | Yang, Lu Wang, Xing Jiao, Xinyan Tian, Bixia Zhang, Miao Zhou, Can Wang, Ruiqi Chen, He Wang, Bo Li, Juan Liu, Jie Zhang, Guanjun Liu, Peijun |
author_facet | Yang, Lu Wang, Xing Jiao, Xinyan Tian, Bixia Zhang, Miao Zhou, Can Wang, Ruiqi Chen, He Wang, Bo Li, Juan Liu, Jie Zhang, Guanjun Liu, Peijun |
author_sort | Yang, Lu |
collection | PubMed |
description | Suppressor of Ty 16 (Spt16) is a component of the facilitates chromatin transcription (FACT) complex, which is a histone chaperone and involved in gene transcription, DNA replication, and DNA repair. Previous studies showed that FACT is highly expressed in cancer, and cancer cells are more reliant on FACT than normal cells. However, the relationship between Spt16 and lung cancer remains unclear. In this study, we explored the functions of Spt16 in lung cancer cells. The effects of Spt16 on lung cancer cell proliferation, cell cycle progression, apoptosis, migration, and invasion were examined. We found that knockdown of Spt16 led to obvious decreases of both Rb and MCM7, and further activated the DNA damage response (DDR) pathway. In addition, a novel micro‐RNA, miR‐1227‐5p, directly targeted the 3′‐UTR of Spt16 and regulated the mRNA levels of Spt16. Furthermore, we found that CBL0137, the functional inhibitor of FACT, showed similar effects as loss of Spt16. Together, our data indicated that Spt16 is likely to be an essential regulator for lung cancer malignancy and is negatively regulated by miR‐1227‐5p. |
format | Online Article Text |
id | pubmed-7648015 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-76480152020-11-16 Suppressor of Ty 16 promotes lung cancer malignancy and is negatively regulated by miR‐1227‐5p Yang, Lu Wang, Xing Jiao, Xinyan Tian, Bixia Zhang, Miao Zhou, Can Wang, Ruiqi Chen, He Wang, Bo Li, Juan Liu, Jie Zhang, Guanjun Liu, Peijun Cancer Sci Original Articles Suppressor of Ty 16 (Spt16) is a component of the facilitates chromatin transcription (FACT) complex, which is a histone chaperone and involved in gene transcription, DNA replication, and DNA repair. Previous studies showed that FACT is highly expressed in cancer, and cancer cells are more reliant on FACT than normal cells. However, the relationship between Spt16 and lung cancer remains unclear. In this study, we explored the functions of Spt16 in lung cancer cells. The effects of Spt16 on lung cancer cell proliferation, cell cycle progression, apoptosis, migration, and invasion were examined. We found that knockdown of Spt16 led to obvious decreases of both Rb and MCM7, and further activated the DNA damage response (DDR) pathway. In addition, a novel micro‐RNA, miR‐1227‐5p, directly targeted the 3′‐UTR of Spt16 and regulated the mRNA levels of Spt16. Furthermore, we found that CBL0137, the functional inhibitor of FACT, showed similar effects as loss of Spt16. Together, our data indicated that Spt16 is likely to be an essential regulator for lung cancer malignancy and is negatively regulated by miR‐1227‐5p. John Wiley and Sons Inc. 2020-09-17 2020-11 /pmc/articles/PMC7648015/ /pubmed/32860308 http://dx.doi.org/10.1111/cas.14627 Text en © 2020 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Articles Yang, Lu Wang, Xing Jiao, Xinyan Tian, Bixia Zhang, Miao Zhou, Can Wang, Ruiqi Chen, He Wang, Bo Li, Juan Liu, Jie Zhang, Guanjun Liu, Peijun Suppressor of Ty 16 promotes lung cancer malignancy and is negatively regulated by miR‐1227‐5p |
title | Suppressor of Ty 16 promotes lung cancer malignancy and is negatively regulated by miR‐1227‐5p |
title_full | Suppressor of Ty 16 promotes lung cancer malignancy and is negatively regulated by miR‐1227‐5p |
title_fullStr | Suppressor of Ty 16 promotes lung cancer malignancy and is negatively regulated by miR‐1227‐5p |
title_full_unstemmed | Suppressor of Ty 16 promotes lung cancer malignancy and is negatively regulated by miR‐1227‐5p |
title_short | Suppressor of Ty 16 promotes lung cancer malignancy and is negatively regulated by miR‐1227‐5p |
title_sort | suppressor of ty 16 promotes lung cancer malignancy and is negatively regulated by mir‐1227‐5p |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7648015/ https://www.ncbi.nlm.nih.gov/pubmed/32860308 http://dx.doi.org/10.1111/cas.14627 |
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