HCG11 up-regulation induced by ELK4 suppressed proliferation in vestibular schwannoma by targeting miR-620/ELK4
Abstract Background Vestibular schwannoma (VS) is a kind of benign tumor deriving from the acoustic nerve sheath. Substantial long non-coding RNAs (lncRNAs) were illustrated to have crucial roles in multiple cancers. However, few lncRNAs were elucidated in VS. Methods HCG11, miR-620 and ELK4 express...
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doaj-8e726d12646c4bf79ab8a48bf45ac36c2021-01-10T12:31:29ZengBMCCancer Cell International1475-28672021-01-0121111010.1186/s12935-020-01691-0HCG11 up-regulation induced by ELK4 suppressed proliferation in vestibular schwannoma by targeting miR-620/ELK4Ruiqing Long0Zhuohui Liu1Jinghui Li2Yuan Zhang3Hualin Yu4Otolaryngology Department, The First Affiliated Hospital of Kunming Medical UniversityOtolaryngology Department, The First Affiliated Hospital of Kunming Medical UniversityNeurosurgery Department, The First Affiliated Hospital of Kunming Medical UniversityOtolaryngology Department, The First Affiliated Hospital of Kunming Medical UniversityNeurosurgery Department, The First Affiliated Hospital of Kunming Medical UniversityAbstract Background Vestibular schwannoma (VS) is a kind of benign tumor deriving from the acoustic nerve sheath. Substantial long non-coding RNAs (lncRNAs) were illustrated to have crucial roles in multiple cancers. However, few lncRNAs were elucidated in VS. Methods HCG11, miR-620 and ELK4 expression were tested by RT-qPCR. Gain-of-function experiments were conducted to confirm the effect of HCG11 on VS. Results HCG11 possessed a low expression in VS cell lines. Overexpression of HCG11 repressed cell proliferation but accelerated apoptosis of VS cells. Moreover, we identified ELK4 stimulated the transcription of HCG11 and their affinity was verified by ChIP assays. MiR-620 was chosen to be a target of HCG11 and it was tested to have a high expression in VS cell lines. Moreover, depletion of miR-620 could inhibit cell proliferative ability while fostering apoptosis rate of VS cells. ELK4 was low expressed in VS cell lines and knockdown of ELK4 could rescue the effects made by HCG11 overexpression on progression of VS. Conclusions HCG11 could inhibit the growth of VS by targeting miR-620/ELK4 in VS cells. HCG11 was a novel therapeutic target for VS treatment.https://doi.org/10.1186/s12935-020-01691-0HCG11miR-620ELK4Vestibular schwannoma |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Ruiqing Long Zhuohui Liu Jinghui Li Yuan Zhang Hualin Yu |
spellingShingle |
Ruiqing Long Zhuohui Liu Jinghui Li Yuan Zhang Hualin Yu HCG11 up-regulation induced by ELK4 suppressed proliferation in vestibular schwannoma by targeting miR-620/ELK4 Cancer Cell International HCG11 miR-620 ELK4 Vestibular schwannoma |
author_facet |
Ruiqing Long Zhuohui Liu Jinghui Li Yuan Zhang Hualin Yu |
author_sort |
Ruiqing Long |
title |
HCG11 up-regulation induced by ELK4 suppressed proliferation in vestibular schwannoma by targeting miR-620/ELK4 |
title_short |
HCG11 up-regulation induced by ELK4 suppressed proliferation in vestibular schwannoma by targeting miR-620/ELK4 |
title_full |
HCG11 up-regulation induced by ELK4 suppressed proliferation in vestibular schwannoma by targeting miR-620/ELK4 |
title_fullStr |
HCG11 up-regulation induced by ELK4 suppressed proliferation in vestibular schwannoma by targeting miR-620/ELK4 |
title_full_unstemmed |
HCG11 up-regulation induced by ELK4 suppressed proliferation in vestibular schwannoma by targeting miR-620/ELK4 |
title_sort |
hcg11 up-regulation induced by elk4 suppressed proliferation in vestibular schwannoma by targeting mir-620/elk4 |
publisher |
BMC |
series |
Cancer Cell International |
issn |
1475-2867 |
publishDate |
2021-01-01 |
description |
Abstract Background Vestibular schwannoma (VS) is a kind of benign tumor deriving from the acoustic nerve sheath. Substantial long non-coding RNAs (lncRNAs) were illustrated to have crucial roles in multiple cancers. However, few lncRNAs were elucidated in VS. Methods HCG11, miR-620 and ELK4 expression were tested by RT-qPCR. Gain-of-function experiments were conducted to confirm the effect of HCG11 on VS. Results HCG11 possessed a low expression in VS cell lines. Overexpression of HCG11 repressed cell proliferation but accelerated apoptosis of VS cells. Moreover, we identified ELK4 stimulated the transcription of HCG11 and their affinity was verified by ChIP assays. MiR-620 was chosen to be a target of HCG11 and it was tested to have a high expression in VS cell lines. Moreover, depletion of miR-620 could inhibit cell proliferative ability while fostering apoptosis rate of VS cells. ELK4 was low expressed in VS cell lines and knockdown of ELK4 could rescue the effects made by HCG11 overexpression on progression of VS. Conclusions HCG11 could inhibit the growth of VS by targeting miR-620/ELK4 in VS cells. HCG11 was a novel therapeutic target for VS treatment. |
topic |
HCG11 miR-620 ELK4 Vestibular schwannoma |
url |
https://doi.org/10.1186/s12935-020-01691-0 |
work_keys_str_mv |
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