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Inhibition of Microrna-766-5p Attenuates the Development of Cervical Cancer Through Regulating SCAI
PURPOSE: MicroRNAs (miRNAs) are considered to play anti-tumor roles in cancers. This study is designed to illustrate the role and potential mechanism of miR-766-5p in cervical cancer (CC) progression. METHODS: MiR-766-5p expression in tissues and serum of CC patients was detected by quantitative rev...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7750902/ https://www.ncbi.nlm.nih.gov/pubmed/33327889 http://dx.doi.org/10.1177/1533033820980081 |
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author | Cai, Yongqin Zhang, Kai Cao, Liya Sun, Hong Wang, Honggang |
author_facet | Cai, Yongqin Zhang, Kai Cao, Liya Sun, Hong Wang, Honggang |
author_sort | Cai, Yongqin |
collection | PubMed |
description | PURPOSE: MicroRNAs (miRNAs) are considered to play anti-tumor roles in cancers. This study is designed to illustrate the role and potential mechanism of miR-766-5p in cervical cancer (CC) progression. METHODS: MiR-766-5p expression in tissues and serum of CC patients was detected by quantitative reverse-transcription PCR (qRT-PCR). Receiver operating characteristic (ROC) curve was performed to evaluate the diagnostic value of serum miR-766-5p in CC. The 5-ethynyl-2′-deoxyuridine (EdU) assay, flow cytometry, wound healing as well as transwell assay were utilized to detect the proliferation, apoptosis, migration and invasion of CC cells, respectively. The interaction between miR-766-5p and SCAI was confirmed by dual-luciferase reporter gene assay. Xenografted tumor model was established to measure the growth of tumor xenograft in vivo. RESULTS: MiR-766-5p was significantly increased in tissues and serum of CC patients. ROC curve suggested that serum miR-766-5p could serve as a biomarker for the diagnosis of CC. Inhibition of miR-766-5p suppressed the proliferation, migration and invasion, and promoted the apoptosis of CC cells. SCAI was proved to be a target of miR-766-5p. Silencing of SCAI eliminated the inhibiting effects of miR-766-5p inhibitor on the proliferation, migration and invasion of CC cells in vitro. Additionally, down-regulation of SCAI also reversed the inhibitory effect of miR-766-5p inhibitor on the growth of tumor xenograft in vivo. CONCLUSIONS: Inhibition of miR-766-5p restrains the cell proliferation, migration and invasion, and promotes the apoptosis in CC through negatively regulating SCAI. |
format | Online Article Text |
id | pubmed-7750902 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-77509022021-01-06 Inhibition of Microrna-766-5p Attenuates the Development of Cervical Cancer Through Regulating SCAI Cai, Yongqin Zhang, Kai Cao, Liya Sun, Hong Wang, Honggang Technol Cancer Res Treat Original Article PURPOSE: MicroRNAs (miRNAs) are considered to play anti-tumor roles in cancers. This study is designed to illustrate the role and potential mechanism of miR-766-5p in cervical cancer (CC) progression. METHODS: MiR-766-5p expression in tissues and serum of CC patients was detected by quantitative reverse-transcription PCR (qRT-PCR). Receiver operating characteristic (ROC) curve was performed to evaluate the diagnostic value of serum miR-766-5p in CC. The 5-ethynyl-2′-deoxyuridine (EdU) assay, flow cytometry, wound healing as well as transwell assay were utilized to detect the proliferation, apoptosis, migration and invasion of CC cells, respectively. The interaction between miR-766-5p and SCAI was confirmed by dual-luciferase reporter gene assay. Xenografted tumor model was established to measure the growth of tumor xenograft in vivo. RESULTS: MiR-766-5p was significantly increased in tissues and serum of CC patients. ROC curve suggested that serum miR-766-5p could serve as a biomarker for the diagnosis of CC. Inhibition of miR-766-5p suppressed the proliferation, migration and invasion, and promoted the apoptosis of CC cells. SCAI was proved to be a target of miR-766-5p. Silencing of SCAI eliminated the inhibiting effects of miR-766-5p inhibitor on the proliferation, migration and invasion of CC cells in vitro. Additionally, down-regulation of SCAI also reversed the inhibitory effect of miR-766-5p inhibitor on the growth of tumor xenograft in vivo. CONCLUSIONS: Inhibition of miR-766-5p restrains the cell proliferation, migration and invasion, and promotes the apoptosis in CC through negatively regulating SCAI. SAGE Publications 2020-12-17 /pmc/articles/PMC7750902/ /pubmed/33327889 http://dx.doi.org/10.1177/1533033820980081 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Article Cai, Yongqin Zhang, Kai Cao, Liya Sun, Hong Wang, Honggang Inhibition of Microrna-766-5p Attenuates the Development of Cervical Cancer Through Regulating SCAI |
title | Inhibition of Microrna-766-5p Attenuates the Development of Cervical Cancer Through Regulating SCAI |
title_full | Inhibition of Microrna-766-5p Attenuates the Development of Cervical Cancer Through Regulating SCAI |
title_fullStr | Inhibition of Microrna-766-5p Attenuates the Development of Cervical Cancer Through Regulating SCAI |
title_full_unstemmed | Inhibition of Microrna-766-5p Attenuates the Development of Cervical Cancer Through Regulating SCAI |
title_short | Inhibition of Microrna-766-5p Attenuates the Development of Cervical Cancer Through Regulating SCAI |
title_sort | inhibition of microrna-766-5p attenuates the development of cervical cancer through regulating scai |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7750902/ https://www.ncbi.nlm.nih.gov/pubmed/33327889 http://dx.doi.org/10.1177/1533033820980081 |
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