Long Non-coding RNAs Contribute to the Inhibition of Proliferation and EMT by Pterostilbene in Human Breast Cancer

Background: There is increasing evidence that long non-coding RNAs (lncRNAs) are involved in the process of carcinogenesis and treatment using chemotherapy. Pterostilbene, a phytochemical agent with natural antioxidant and anti-inflammatory properties, has been shown to modulate oncogenic processes...

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Main Authors: Yongye Huang, Juan Du, Yan Mi, Tianye Li, Ying Gong, Hongsheng Ouyang, Yue Hou
Format: Article
Language:English
Published: Frontiers Media S.A. 2018-12-01
Series:Frontiers in Oncology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fonc.2018.00629/full
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author Yongye Huang
Juan Du
Yan Mi
Tianye Li
Ying Gong
Hongsheng Ouyang
Yue Hou
author_facet Yongye Huang
Juan Du
Yan Mi
Tianye Li
Ying Gong
Hongsheng Ouyang
Yue Hou
author_sort Yongye Huang
collection DOAJ
description Background: There is increasing evidence that long non-coding RNAs (lncRNAs) are involved in the process of carcinogenesis and treatment using chemotherapy. Pterostilbene, a phytochemical agent with natural antioxidant and anti-inflammatory properties, has been shown to modulate oncogenic processes in many cancers. However, there has been limited research on the association between pterostilbene and the expression of lncRNAs.Methods: MCF7 breast cancer cells were treated with various concentrations of pterostilbene and their gene expression profile was analyzed by quantitative real-time PCR, Western blotting and immunofluorescence.Results: Treatment with pterostilbene inhibited cell proliferation and epithelial-to-mesenchymal transition (EMT), and increased cell apoptosis, autophagy and ER stress. The Akt/mTOR pathway was downregulated, but p38 MAPK/Erk signaling was activated in cells following treatment with pterostilbene. Pterostilbene increased the expression of the lncRNAs MEG3, TUG1, H19, and DICER1-AS1 whereas the expression of LINC01121, PTTG3P, and HOTAIR declined. Knockdown of lncRNA H19 resulted in a reduction of the cell invasion, with the cells becoming more sensitive to pterostilbene therapy.Conclusions: These results suggest that efficient optimum disruption of lncRNA expression might possibly improve the anti-tumor effects of phytochemical agents, thus serving as a potential therapy for breast cancer.
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spelling doaj.art-e56f5cac52b24f65bb2447f2e83c15a12022-12-22T03:50:04ZengFrontiers Media S.A.Frontiers in Oncology2234-943X2018-12-01810.3389/fonc.2018.00629426626Long Non-coding RNAs Contribute to the Inhibition of Proliferation and EMT by Pterostilbene in Human Breast CancerYongye Huang0Juan Du1Yan Mi2Tianye Li3Ying Gong4Hongsheng Ouyang5Yue Hou6College of Life and Health Sciences, Northeastern University, Shenyang, ChinaCollege of Life and Health Sciences, Northeastern University, Shenyang, ChinaCollege of Life and Health Sciences, Northeastern University, Shenyang, ChinaCollege of Life and Health Sciences, Northeastern University, Shenyang, ChinaCollege of Life and Health Sciences, Northeastern University, Shenyang, ChinaJilin Provincial Key Laboratory of Animal Embryo Engineering, College of Animal Sciences, Jilin University, Changchun, ChinaCollege of Life and Health Sciences, Northeastern University, Shenyang, ChinaBackground: There is increasing evidence that long non-coding RNAs (lncRNAs) are involved in the process of carcinogenesis and treatment using chemotherapy. Pterostilbene, a phytochemical agent with natural antioxidant and anti-inflammatory properties, has been shown to modulate oncogenic processes in many cancers. However, there has been limited research on the association between pterostilbene and the expression of lncRNAs.Methods: MCF7 breast cancer cells were treated with various concentrations of pterostilbene and their gene expression profile was analyzed by quantitative real-time PCR, Western blotting and immunofluorescence.Results: Treatment with pterostilbene inhibited cell proliferation and epithelial-to-mesenchymal transition (EMT), and increased cell apoptosis, autophagy and ER stress. The Akt/mTOR pathway was downregulated, but p38 MAPK/Erk signaling was activated in cells following treatment with pterostilbene. Pterostilbene increased the expression of the lncRNAs MEG3, TUG1, H19, and DICER1-AS1 whereas the expression of LINC01121, PTTG3P, and HOTAIR declined. Knockdown of lncRNA H19 resulted in a reduction of the cell invasion, with the cells becoming more sensitive to pterostilbene therapy.Conclusions: These results suggest that efficient optimum disruption of lncRNA expression might possibly improve the anti-tumor effects of phytochemical agents, thus serving as a potential therapy for breast cancer.https://www.frontiersin.org/article/10.3389/fonc.2018.00629/fullpterostilbenelncRNAscancerautophagyepithelial-to-mesenchymal transition
spellingShingle Yongye Huang
Juan Du
Yan Mi
Tianye Li
Ying Gong
Hongsheng Ouyang
Yue Hou
Long Non-coding RNAs Contribute to the Inhibition of Proliferation and EMT by Pterostilbene in Human Breast Cancer
Frontiers in Oncology
pterostilbene
lncRNAs
cancer
autophagy
epithelial-to-mesenchymal transition
title Long Non-coding RNAs Contribute to the Inhibition of Proliferation and EMT by Pterostilbene in Human Breast Cancer
title_full Long Non-coding RNAs Contribute to the Inhibition of Proliferation and EMT by Pterostilbene in Human Breast Cancer
title_fullStr Long Non-coding RNAs Contribute to the Inhibition of Proliferation and EMT by Pterostilbene in Human Breast Cancer
title_full_unstemmed Long Non-coding RNAs Contribute to the Inhibition of Proliferation and EMT by Pterostilbene in Human Breast Cancer
title_short Long Non-coding RNAs Contribute to the Inhibition of Proliferation and EMT by Pterostilbene in Human Breast Cancer
title_sort long non coding rnas contribute to the inhibition of proliferation and emt by pterostilbene in human breast cancer
topic pterostilbene
lncRNAs
cancer
autophagy
epithelial-to-mesenchymal transition
url https://www.frontiersin.org/article/10.3389/fonc.2018.00629/full
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