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...
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Online Access: | https://doi.org/10.1002/kjm2.12273 |
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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 |
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