Cargando…

Upregulation of MicroRNA-34a Sensitizes Ovarian Cancer Cells to Resveratrol by Targeting Bcl-2

PURPOSE: Resveratrol (REV), a natural compound found in red wine, exhibits antitumor activity in various cancers, including ovarian cancer (OC). However, its potential anti-tumor mechanisms in OC are not well characterized. Here, we tried to elucidate the underlying mechanisms of REV in OC cells. MA...

Descripción completa

Detalles Bibliográficos
Autores principales: Yao, Shangli, Gao, Ming, Wang, Zujun, Wang, Wenyan, Zhan, Lei, Wei, Bing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Yonsei University College of Medicine 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8298871/
https://www.ncbi.nlm.nih.gov/pubmed/34296546
http://dx.doi.org/10.3349/ymj.2021.62.8.691
_version_ 1783726145191018496
author Yao, Shangli
Gao, Ming
Wang, Zujun
Wang, Wenyan
Zhan, Lei
Wei, Bing
author_facet Yao, Shangli
Gao, Ming
Wang, Zujun
Wang, Wenyan
Zhan, Lei
Wei, Bing
author_sort Yao, Shangli
collection PubMed
description PURPOSE: Resveratrol (REV), a natural compound found in red wine, exhibits antitumor activity in various cancers, including ovarian cancer (OC). However, its potential anti-tumor mechanisms in OC are not well characterized. Here, we tried to elucidate the underlying mechanisms of REV in OC cells. MATERIALS AND METHODS: The anti-proliferative effects of REV against OC cells were measured using CCK-8 assay. Apoptosis was measured using an Annexin V-FITC/PI apoptosis detection kit. The anti-metastasis effects of REV were evaluated by invasion assay and wound healing assay. The miRNA profiles in REV-treated cells were determined by microarray assay. RESULTS: Our results showed that REV treatment suppresses the proliferation, induces the apoptosis, and inhibits the invasion and migration of OV-90 and SKOV-3 cells. miR-34a was selected for further study due to its tumor suppressive roles in various human cancers. We found miR-34a overexpression enhanced the inhibitory effects of REV on OC cells, whereas miR-34a inhibition had the opposite effect in OC cells. In addition, we verified that BCL2, an anti-apoptotic gene, was found directly targeted by miR-34a. We also found that REV reduced the expression of Bcl-2 in OC cells. Further investigations revealed that overexpression of Bcl-2 significantly abolished the anti-tumor effects of REV on OC cells. CONCLUSION: Overall, these results demonstrated that REV exerts anti-cancer effects on OC cells through an miR-34a/Bcl-2 axis, highlighting the therapeutic potential of REV for treatment of OC.
format Online
Article
Text
id pubmed-8298871
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Yonsei University College of Medicine
record_format MEDLINE/PubMed
spelling pubmed-82988712021-08-03 Upregulation of MicroRNA-34a Sensitizes Ovarian Cancer Cells to Resveratrol by Targeting Bcl-2 Yao, Shangli Gao, Ming Wang, Zujun Wang, Wenyan Zhan, Lei Wei, Bing Yonsei Med J Original Article PURPOSE: Resveratrol (REV), a natural compound found in red wine, exhibits antitumor activity in various cancers, including ovarian cancer (OC). However, its potential anti-tumor mechanisms in OC are not well characterized. Here, we tried to elucidate the underlying mechanisms of REV in OC cells. MATERIALS AND METHODS: The anti-proliferative effects of REV against OC cells were measured using CCK-8 assay. Apoptosis was measured using an Annexin V-FITC/PI apoptosis detection kit. The anti-metastasis effects of REV were evaluated by invasion assay and wound healing assay. The miRNA profiles in REV-treated cells were determined by microarray assay. RESULTS: Our results showed that REV treatment suppresses the proliferation, induces the apoptosis, and inhibits the invasion and migration of OV-90 and SKOV-3 cells. miR-34a was selected for further study due to its tumor suppressive roles in various human cancers. We found miR-34a overexpression enhanced the inhibitory effects of REV on OC cells, whereas miR-34a inhibition had the opposite effect in OC cells. In addition, we verified that BCL2, an anti-apoptotic gene, was found directly targeted by miR-34a. We also found that REV reduced the expression of Bcl-2 in OC cells. Further investigations revealed that overexpression of Bcl-2 significantly abolished the anti-tumor effects of REV on OC cells. CONCLUSION: Overall, these results demonstrated that REV exerts anti-cancer effects on OC cells through an miR-34a/Bcl-2 axis, highlighting the therapeutic potential of REV for treatment of OC. Yonsei University College of Medicine 2021-08-01 2021-07-19 /pmc/articles/PMC8298871/ /pubmed/34296546 http://dx.doi.org/10.3349/ymj.2021.62.8.691 Text en © Copyright: Yonsei University College of Medicine 2021 https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Yao, Shangli
Gao, Ming
Wang, Zujun
Wang, Wenyan
Zhan, Lei
Wei, Bing
Upregulation of MicroRNA-34a Sensitizes Ovarian Cancer Cells to Resveratrol by Targeting Bcl-2
title Upregulation of MicroRNA-34a Sensitizes Ovarian Cancer Cells to Resveratrol by Targeting Bcl-2
title_full Upregulation of MicroRNA-34a Sensitizes Ovarian Cancer Cells to Resveratrol by Targeting Bcl-2
title_fullStr Upregulation of MicroRNA-34a Sensitizes Ovarian Cancer Cells to Resveratrol by Targeting Bcl-2
title_full_unstemmed Upregulation of MicroRNA-34a Sensitizes Ovarian Cancer Cells to Resveratrol by Targeting Bcl-2
title_short Upregulation of MicroRNA-34a Sensitizes Ovarian Cancer Cells to Resveratrol by Targeting Bcl-2
title_sort upregulation of microrna-34a sensitizes ovarian cancer cells to resveratrol by targeting bcl-2
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8298871/
https://www.ncbi.nlm.nih.gov/pubmed/34296546
http://dx.doi.org/10.3349/ymj.2021.62.8.691
work_keys_str_mv AT yaoshangli upregulationofmicrorna34asensitizesovariancancercellstoresveratrolbytargetingbcl2
AT gaoming upregulationofmicrorna34asensitizesovariancancercellstoresveratrolbytargetingbcl2
AT wangzujun upregulationofmicrorna34asensitizesovariancancercellstoresveratrolbytargetingbcl2
AT wangwenyan upregulationofmicrorna34asensitizesovariancancercellstoresveratrolbytargetingbcl2
AT zhanlei upregulationofmicrorna34asensitizesovariancancercellstoresveratrolbytargetingbcl2
AT weibing upregulationofmicrorna34asensitizesovariancancercellstoresveratrolbytargetingbcl2