MicroRNA-223 Targeting STIM1 Inhibits the Biological Behavior of Breast Cancer

Background/Aims: To investigate the cellular effects and clinical significance of microRNA-223 (miR-223) in breast cancer by targeting stromal interaction molecule1 (STIM1). Methods: Breast cancer cell lines (T47D, MCF-7, SKB-R3, MDA-MB-231 and MDA-MB-435) and a normal breast epithelial cell line (M...

Full description

Bibliographic Details
Main Authors: Yanfang Yang, Zhansheng Jiang, Ning Ma, Bin Wang, Jun Liu, Lina Zhang, Lin Gu
Format: Article
Language:English
Published: Cell Physiol Biochem Press GmbH & Co KG 2018-01-01
Series:Cellular Physiology and Biochemistry
Subjects:
Online Access:https://www.karger.com/Article/FullText/487180
_version_ 1819263018838523904
author Yanfang Yang
Zhansheng Jiang
Ning Ma
Bin Wang
Jun Liu
Lina Zhang
Lin Gu
author_facet Yanfang Yang
Zhansheng Jiang
Ning Ma
Bin Wang
Jun Liu
Lina Zhang
Lin Gu
author_sort Yanfang Yang
collection DOAJ
description Background/Aims: To investigate the cellular effects and clinical significance of microRNA-223 (miR-223) in breast cancer by targeting stromal interaction molecule1 (STIM1). Methods: Breast cancer cell lines (T47D, MCF-7, SKB-R3, MDA-MB-231 and MDA-MB-435) and a normal breast epithelial cell line (MCF-10A) were prepared for this study. MiR-223 mimics, anti-miR-223 and pcDNA 3.1-STIM1 were transiently transfected into cancer cells independently or together, and then RT-qPCR was performed to detect the expressions of miR-223 and STIM1 mRNA, dual-luciferase reporter assay was conducted to examine the effects of miR-223 on STIM1, Western blotting was used to measure the expressions of the STIM1 proteins, MTT and Trans-well assays were performed to detect cell proliferation and invasion. Finally, the correlation of miR-223 and STIM1 was investigated by detecting with ISH and IHC in breast cancer specimens or the corresponding adjacent normal tissues. Results: Compared with normal cells and tissues, breast cancer tissues and cells exhibited significantly lower expression of miR-223, but higher expression of STIM1. MiR-223 could inhibit the proliferation and invasiveness of breast cancer cells by negatively regulating the expressions of STIM1. Reimplantation with STIM1 partially rescued the miRNA-223-induced inhibition of breast cancer cells. Clinical data revealed that high expression of STIM1 and miR-223 was respectively detrimental and beneficial factor impacting patient’s disease-free survival (DFS) rather than overall survival (OS). Moreover, Pearson correlation analysis also confirmed that STIM1 was inversely correlated with miR-223. Conclusion: MiR-223 inhibits the proliferation and invasion of breast cancer by targeting STIM1. The miR-223/STIM1 axis could possibly be a potential therapeutic target for treating breast cancer patients.
first_indexed 2024-12-23T20:06:55Z
format Article
id doaj.art-08174d118c744fb39bf83674900c5e31
institution Directory Open Access Journal
issn 1015-8987
1421-9778
language English
last_indexed 2024-12-23T20:06:55Z
publishDate 2018-01-01
publisher Cell Physiol Biochem Press GmbH & Co KG
record_format Article
series Cellular Physiology and Biochemistry
spelling doaj.art-08174d118c744fb39bf83674900c5e312022-12-21T17:32:54ZengCell Physiol Biochem Press GmbH & Co KGCellular Physiology and Biochemistry1015-89871421-97782018-01-0145285686610.1159/000487180487180MicroRNA-223 Targeting STIM1 Inhibits the Biological Behavior of Breast CancerYanfang YangZhansheng JiangNing MaBin WangJun LiuLina ZhangLin GuBackground/Aims: To investigate the cellular effects and clinical significance of microRNA-223 (miR-223) in breast cancer by targeting stromal interaction molecule1 (STIM1). Methods: Breast cancer cell lines (T47D, MCF-7, SKB-R3, MDA-MB-231 and MDA-MB-435) and a normal breast epithelial cell line (MCF-10A) were prepared for this study. MiR-223 mimics, anti-miR-223 and pcDNA 3.1-STIM1 were transiently transfected into cancer cells independently or together, and then RT-qPCR was performed to detect the expressions of miR-223 and STIM1 mRNA, dual-luciferase reporter assay was conducted to examine the effects of miR-223 on STIM1, Western blotting was used to measure the expressions of the STIM1 proteins, MTT and Trans-well assays were performed to detect cell proliferation and invasion. Finally, the correlation of miR-223 and STIM1 was investigated by detecting with ISH and IHC in breast cancer specimens or the corresponding adjacent normal tissues. Results: Compared with normal cells and tissues, breast cancer tissues and cells exhibited significantly lower expression of miR-223, but higher expression of STIM1. MiR-223 could inhibit the proliferation and invasiveness of breast cancer cells by negatively regulating the expressions of STIM1. Reimplantation with STIM1 partially rescued the miRNA-223-induced inhibition of breast cancer cells. Clinical data revealed that high expression of STIM1 and miR-223 was respectively detrimental and beneficial factor impacting patient’s disease-free survival (DFS) rather than overall survival (OS). Moreover, Pearson correlation analysis also confirmed that STIM1 was inversely correlated with miR-223. Conclusion: MiR-223 inhibits the proliferation and invasion of breast cancer by targeting STIM1. The miR-223/STIM1 axis could possibly be a potential therapeutic target for treating breast cancer patients.https://www.karger.com/Article/FullText/487180MicrornaMiR-223Stromal interaction molecule1Breast cancerProliferationInvasion
spellingShingle Yanfang Yang
Zhansheng Jiang
Ning Ma
Bin Wang
Jun Liu
Lina Zhang
Lin Gu
MicroRNA-223 Targeting STIM1 Inhibits the Biological Behavior of Breast Cancer
Cellular Physiology and Biochemistry
Microrna
MiR-223
Stromal interaction molecule1
Breast cancer
Proliferation
Invasion
title MicroRNA-223 Targeting STIM1 Inhibits the Biological Behavior of Breast Cancer
title_full MicroRNA-223 Targeting STIM1 Inhibits the Biological Behavior of Breast Cancer
title_fullStr MicroRNA-223 Targeting STIM1 Inhibits the Biological Behavior of Breast Cancer
title_full_unstemmed MicroRNA-223 Targeting STIM1 Inhibits the Biological Behavior of Breast Cancer
title_short MicroRNA-223 Targeting STIM1 Inhibits the Biological Behavior of Breast Cancer
title_sort microrna 223 targeting stim1 inhibits the biological behavior of breast cancer
topic Microrna
MiR-223
Stromal interaction molecule1
Breast cancer
Proliferation
Invasion
url https://www.karger.com/Article/FullText/487180
work_keys_str_mv AT yanfangyang microrna223targetingstim1inhibitsthebiologicalbehaviorofbreastcancer
AT zhanshengjiang microrna223targetingstim1inhibitsthebiologicalbehaviorofbreastcancer
AT ningma microrna223targetingstim1inhibitsthebiologicalbehaviorofbreastcancer
AT binwang microrna223targetingstim1inhibitsthebiologicalbehaviorofbreastcancer
AT junliu microrna223targetingstim1inhibitsthebiologicalbehaviorofbreastcancer
AT linazhang microrna223targetingstim1inhibitsthebiologicalbehaviorofbreastcancer
AT lingu microrna223targetingstim1inhibitsthebiologicalbehaviorofbreastcancer