MiR-375 Is Epigenetically Downregulated by HPV-16 E6 Mediated DNMT1 Upregulation and Modulates EMT of Cervical Cancer Cells by Suppressing lncRNA MALAT1.

Epigenetic modulation is an important mechanism of miRNA dysregulation in cervical cancer. In this study, we firstly studied how this mechanism contributes to miR-375 downregulation in cervical cancer cells. Then, we further studied the association between miR-375 and MALAT1 (metastasis associated l...

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Main Authors: Shikai Liu, Lili Song, Hairong Yao, Liang Zhang, Dongkui Xu, Fangyuan Gao, Qian Li
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2016-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC5033370?pdf=render
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author Shikai Liu
Lili Song
Hairong Yao
Liang Zhang
Dongkui Xu
Fangyuan Gao
Qian Li
author_facet Shikai Liu
Lili Song
Hairong Yao
Liang Zhang
Dongkui Xu
Fangyuan Gao
Qian Li
author_sort Shikai Liu
collection DOAJ
description Epigenetic modulation is an important mechanism of miRNA dysregulation in cervical cancer. In this study, we firstly studied how this mechanism contributes to miR-375 downregulation in cervical cancer cells. Then, we further studied the association between miR-375 and MALAT1 (metastasis associated lung adenocarcinoma transcript 1) in epithelial mesenchymal transition (EMT) of the cancer cells. HPV-16 positive SiHa and CaSki cells were used as in vitro model. Our data showed that HPV-16 E6 positively modulated DNMT1 expression in both SiHa and CaSki cells. Knockdown of DNMT1 partly restored miR-375 levels in the cells. The following methylation-specific PCR (MSP) assay and qRT-PCR analysis showed that methylation was common in the promoter region of miR-375 in both SiHa and CaSki cells and demethylation partly restored miR-375 levels in the cells. Therefore, we infer that miR-375 is downregulated partly due to promoter hypermethylation mediated by DNMT1 in HPV-16 positive cervical cancer cells. Our bioinformatics analysis showed that MALAT1 has three putative binding sites with miR-375 and the following dual luciferase assay confirmed two of them. QRT-PCR analysis showed that miR-375 overexpression significantly reduced MALAT1 expression, while MALAT1 overexpression reversely suppressed miR-375 levels. Therefore, we infer that there is a reciprocal regulation between miR-375 and MALAT1 in the cells. In SiHa cells, miR-375 overexpression or MALAT1 siRNA partly restored E-cadherin expression, significantly reduced N-cadherin and also reduced invasion capacity of SiHa cells. Therefore, these results suggest that miR-375 and MALAT1 form a functional axis modulating EMT in cervical cancer.
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spelling doaj.art-890666f8f2794273980a27f0228db86a2022-12-22T01:15:11ZengPublic Library of Science (PLoS)PLoS ONE1932-62032016-01-01119e016346010.1371/journal.pone.0163460MiR-375 Is Epigenetically Downregulated by HPV-16 E6 Mediated DNMT1 Upregulation and Modulates EMT of Cervical Cancer Cells by Suppressing lncRNA MALAT1.Shikai LiuLili SongHairong YaoLiang ZhangDongkui XuFangyuan GaoQian LiEpigenetic modulation is an important mechanism of miRNA dysregulation in cervical cancer. In this study, we firstly studied how this mechanism contributes to miR-375 downregulation in cervical cancer cells. Then, we further studied the association between miR-375 and MALAT1 (metastasis associated lung adenocarcinoma transcript 1) in epithelial mesenchymal transition (EMT) of the cancer cells. HPV-16 positive SiHa and CaSki cells were used as in vitro model. Our data showed that HPV-16 E6 positively modulated DNMT1 expression in both SiHa and CaSki cells. Knockdown of DNMT1 partly restored miR-375 levels in the cells. The following methylation-specific PCR (MSP) assay and qRT-PCR analysis showed that methylation was common in the promoter region of miR-375 in both SiHa and CaSki cells and demethylation partly restored miR-375 levels in the cells. Therefore, we infer that miR-375 is downregulated partly due to promoter hypermethylation mediated by DNMT1 in HPV-16 positive cervical cancer cells. Our bioinformatics analysis showed that MALAT1 has three putative binding sites with miR-375 and the following dual luciferase assay confirmed two of them. QRT-PCR analysis showed that miR-375 overexpression significantly reduced MALAT1 expression, while MALAT1 overexpression reversely suppressed miR-375 levels. Therefore, we infer that there is a reciprocal regulation between miR-375 and MALAT1 in the cells. In SiHa cells, miR-375 overexpression or MALAT1 siRNA partly restored E-cadherin expression, significantly reduced N-cadherin and also reduced invasion capacity of SiHa cells. Therefore, these results suggest that miR-375 and MALAT1 form a functional axis modulating EMT in cervical cancer.http://europepmc.org/articles/PMC5033370?pdf=render
spellingShingle Shikai Liu
Lili Song
Hairong Yao
Liang Zhang
Dongkui Xu
Fangyuan Gao
Qian Li
MiR-375 Is Epigenetically Downregulated by HPV-16 E6 Mediated DNMT1 Upregulation and Modulates EMT of Cervical Cancer Cells by Suppressing lncRNA MALAT1.
PLoS ONE
title MiR-375 Is Epigenetically Downregulated by HPV-16 E6 Mediated DNMT1 Upregulation and Modulates EMT of Cervical Cancer Cells by Suppressing lncRNA MALAT1.
title_full MiR-375 Is Epigenetically Downregulated by HPV-16 E6 Mediated DNMT1 Upregulation and Modulates EMT of Cervical Cancer Cells by Suppressing lncRNA MALAT1.
title_fullStr MiR-375 Is Epigenetically Downregulated by HPV-16 E6 Mediated DNMT1 Upregulation and Modulates EMT of Cervical Cancer Cells by Suppressing lncRNA MALAT1.
title_full_unstemmed MiR-375 Is Epigenetically Downregulated by HPV-16 E6 Mediated DNMT1 Upregulation and Modulates EMT of Cervical Cancer Cells by Suppressing lncRNA MALAT1.
title_short MiR-375 Is Epigenetically Downregulated by HPV-16 E6 Mediated DNMT1 Upregulation and Modulates EMT of Cervical Cancer Cells by Suppressing lncRNA MALAT1.
title_sort mir 375 is epigenetically downregulated by hpv 16 e6 mediated dnmt1 upregulation and modulates emt of cervical cancer cells by suppressing lncrna malat1
url http://europepmc.org/articles/PMC5033370?pdf=render
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AT lilisong mir375isepigeneticallydownregulatedbyhpv16e6mediateddnmt1upregulationandmodulatesemtofcervicalcancercellsbysuppressinglncrnamalat1
AT hairongyao mir375isepigeneticallydownregulatedbyhpv16e6mediateddnmt1upregulationandmodulatesemtofcervicalcancercellsbysuppressinglncrnamalat1
AT liangzhang mir375isepigeneticallydownregulatedbyhpv16e6mediateddnmt1upregulationandmodulatesemtofcervicalcancercellsbysuppressinglncrnamalat1
AT dongkuixu mir375isepigeneticallydownregulatedbyhpv16e6mediateddnmt1upregulationandmodulatesemtofcervicalcancercellsbysuppressinglncrnamalat1
AT fangyuangao mir375isepigeneticallydownregulatedbyhpv16e6mediateddnmt1upregulationandmodulatesemtofcervicalcancercellsbysuppressinglncrnamalat1
AT qianli mir375isepigeneticallydownregulatedbyhpv16e6mediateddnmt1upregulationandmodulatesemtofcervicalcancercellsbysuppressinglncrnamalat1