miR-183-5p Aggravates Breast Cancer Development via Mediation of RGS2
This study mainly explores how miR-183-5p pertains to breast cancer (BC) development. Functional assays were employed to test impacts of miR-183-5p in this cancer. Targeting between RGS2 and miR-183-5p was examined with dual-luciferase assay, and how their interaction pertains to cancer progression...
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Hindawi Limited
2021
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oai:doaj.org-article:2170496e51384586bb5fc1c09422d42c2021-11-29T00:56:16ZmiR-183-5p Aggravates Breast Cancer Development via Mediation of RGS21748-671810.1155/2021/9664195https://doaj.org/article/2170496e51384586bb5fc1c09422d42c2021-01-01T00:00:00Zhttp://dx.doi.org/10.1155/2021/9664195https://doaj.org/toc/1748-6718This study mainly explores how miR-183-5p pertains to breast cancer (BC) development. Functional assays were employed to test impacts of miR-183-5p in this cancer. Targeting between RGS2 and miR-183-5p was examined with dual-luciferase assay, and how their interaction pertains to cancer progression was further unraveled. miR-183-5p level was noticeably high in cancer tissue/cells. Overexpressing miR-183-5p could remarkably deteriorate cancer progression. The regulatory gene RGS2 levels was markedly low in BC, and two genes we researched were negatively correlated. It was uncovered by rescue assay that miR-183-5p/RGS2 axis mediated tumor-relevant behaviors in BC. Altogether, miR-183-5p aggravates BC development via mediation of RGS2. miR-183-5p supplies a promising target for BC therapy.Chihua WuYoulin TuoGang HuJing LuoHindawi LimitedarticleComputer applications to medicine. Medical informaticsR858-859.7ENComputational and Mathematical Methods in Medicine, Vol 2021 (2021) |
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Computer applications to medicine. Medical informatics R858-859.7 |
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Computer applications to medicine. Medical informatics R858-859.7 Chihua Wu Youlin Tuo Gang Hu Jing Luo miR-183-5p Aggravates Breast Cancer Development via Mediation of RGS2 |
description |
This study mainly explores how miR-183-5p pertains to breast cancer (BC) development. Functional assays were employed to test impacts of miR-183-5p in this cancer. Targeting between RGS2 and miR-183-5p was examined with dual-luciferase assay, and how their interaction pertains to cancer progression was further unraveled. miR-183-5p level was noticeably high in cancer tissue/cells. Overexpressing miR-183-5p could remarkably deteriorate cancer progression. The regulatory gene RGS2 levels was markedly low in BC, and two genes we researched were negatively correlated. It was uncovered by rescue assay that miR-183-5p/RGS2 axis mediated tumor-relevant behaviors in BC. Altogether, miR-183-5p aggravates BC development via mediation of RGS2. miR-183-5p supplies a promising target for BC therapy. |
format |
article |
author |
Chihua Wu Youlin Tuo Gang Hu Jing Luo |
author_facet |
Chihua Wu Youlin Tuo Gang Hu Jing Luo |
author_sort |
Chihua Wu |
title |
miR-183-5p Aggravates Breast Cancer Development via Mediation of RGS2 |
title_short |
miR-183-5p Aggravates Breast Cancer Development via Mediation of RGS2 |
title_full |
miR-183-5p Aggravates Breast Cancer Development via Mediation of RGS2 |
title_fullStr |
miR-183-5p Aggravates Breast Cancer Development via Mediation of RGS2 |
title_full_unstemmed |
miR-183-5p Aggravates Breast Cancer Development via Mediation of RGS2 |
title_sort |
mir-183-5p aggravates breast cancer development via mediation of rgs2 |
publisher |
Hindawi Limited |
publishDate |
2021 |
url |
https://doaj.org/article/2170496e51384586bb5fc1c09422d42c |
work_keys_str_mv |
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_version_ |
1718407693380616192 |