Inhibiting microRNA‐301b suppresses cell growth and targets RNF38 in cervical carcinoma

Abstract It has been reported microRNA‐301b (miR‐301b) was involved in the tumorigenesis of some cancers, but it has not been investigated in cervical carcinoma yet. In this study, miR‐301b was found significantly upregulated in cervical carcinoma, and patients with high miR‐301b expression had a sh...

Full description

Bibliographic Details
Main Authors: Wen‐Ling Guo, Ning Li, Jian‐Lin Ma, Xue‐Mei Chen, Fan‐Ying Shi
Format: Article
Language:English
Published: Wiley 2020-11-01
Series:Kaohsiung Journal of Medical Sciences
Subjects:
Online Access:https://doi.org/10.1002/kjm2.12273
id doaj-8b3db8c423ec44398008ba445b4d1274
record_format Article
spelling doaj-8b3db8c423ec44398008ba445b4d12742020-11-25T04:10:29ZengWileyKaohsiung Journal of Medical Sciences1607-551X2410-86502020-11-01361187888410.1002/kjm2.12273Inhibiting microRNA‐301b suppresses cell growth and targets RNF38 in cervical carcinomaWen‐Ling Guo0Ning Li1Jian‐Lin Ma2Xue‐Mei Chen3Fan‐Ying Shi4Department of Obstetrics Binzhou Central Hospital Binzhou Shandong ChinaDepartment of Obstetrics Binzhou Central Hospital Binzhou Shandong ChinaDepartment of Emergency Binzhou Central Hospital Binzhou Shandong ChinaDepartment of Obstetrics Binzhou Central Hospital Binzhou Shandong ChinaDepartment of Obstetrics Binzhou Central Hospital Binzhou Shandong ChinaAbstract It has been reported microRNA‐301b (miR‐301b) was involved in the tumorigenesis of some cancers, but it has not been investigated in cervical carcinoma yet. In this study, miR‐301b was found significantly upregulated in cervical carcinoma, and patients with high miR‐301b expression had a shorter overall survival. When miR‐301b was knocked down in cervical carcinoma cells, the cell growth could be significantly abolished. Our further studies showed miR‐301b targeted RNF38, and inhibited its expression in cervical carcinoma cells. Moreover, RNF38 was found downregulated in cervical carcinoma, and miR‐301b expression in cervical tissues was found negatively correlated with RNF38 expression. In addition, overexpression of RNF38 significantly inhibited cervical carcinoma cell growth, but overexpression of miR‐301b suppressed RNF38‐induced cell growth inhibition in cervical carcinoma. Collectively, this study suggested miR‐301b could be a novel target for cervical carcinoma treatment.https://doi.org/10.1002/kjm2.12273cell growthcervical carcinomamicroRNA‐301bRNF38
collection DOAJ
language English
format Article
sources DOAJ
author Wen‐Ling Guo
Ning Li
Jian‐Lin Ma
Xue‐Mei Chen
Fan‐Ying Shi
spellingShingle Wen‐Ling Guo
Ning Li
Jian‐Lin Ma
Xue‐Mei Chen
Fan‐Ying Shi
Inhibiting microRNA‐301b suppresses cell growth and targets RNF38 in cervical carcinoma
Kaohsiung Journal of Medical Sciences
cell growth
cervical carcinoma
microRNA‐301b
RNF38
author_facet Wen‐Ling Guo
Ning Li
Jian‐Lin Ma
Xue‐Mei Chen
Fan‐Ying Shi
author_sort Wen‐Ling Guo
title Inhibiting microRNA‐301b suppresses cell growth and targets RNF38 in cervical carcinoma
title_short Inhibiting microRNA‐301b suppresses cell growth and targets RNF38 in cervical carcinoma
title_full Inhibiting microRNA‐301b suppresses cell growth and targets RNF38 in cervical carcinoma
title_fullStr Inhibiting microRNA‐301b suppresses cell growth and targets RNF38 in cervical carcinoma
title_full_unstemmed Inhibiting microRNA‐301b suppresses cell growth and targets RNF38 in cervical carcinoma
title_sort inhibiting microrna‐301b suppresses cell growth and targets rnf38 in cervical carcinoma
publisher Wiley
series Kaohsiung Journal of Medical Sciences
issn 1607-551X
2410-8650
publishDate 2020-11-01
description Abstract It has been reported microRNA‐301b (miR‐301b) was involved in the tumorigenesis of some cancers, but it has not been investigated in cervical carcinoma yet. In this study, miR‐301b was found significantly upregulated in cervical carcinoma, and patients with high miR‐301b expression had a shorter overall survival. When miR‐301b was knocked down in cervical carcinoma cells, the cell growth could be significantly abolished. Our further studies showed miR‐301b targeted RNF38, and inhibited its expression in cervical carcinoma cells. Moreover, RNF38 was found downregulated in cervical carcinoma, and miR‐301b expression in cervical tissues was found negatively correlated with RNF38 expression. In addition, overexpression of RNF38 significantly inhibited cervical carcinoma cell growth, but overexpression of miR‐301b suppressed RNF38‐induced cell growth inhibition in cervical carcinoma. Collectively, this study suggested miR‐301b could be a novel target for cervical carcinoma treatment.
topic cell growth
cervical carcinoma
microRNA‐301b
RNF38
url https://doi.org/10.1002/kjm2.12273
work_keys_str_mv AT wenlingguo inhibitingmicrorna301bsuppressescellgrowthandtargetsrnf38incervicalcarcinoma
AT ningli inhibitingmicrorna301bsuppressescellgrowthandtargetsrnf38incervicalcarcinoma
AT jianlinma inhibitingmicrorna301bsuppressescellgrowthandtargetsrnf38incervicalcarcinoma
AT xuemeichen inhibitingmicrorna301bsuppressescellgrowthandtargetsrnf38incervicalcarcinoma
AT fanyingshi inhibitingmicrorna301bsuppressescellgrowthandtargetsrnf38incervicalcarcinoma
_version_ 1724420543567888384