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MiR-320a acts as a prognostic factor and Inhibits metastasis of salivary adenoid cystic carcinoma by targeting ITGB3

BACKGROUND: Salivary Adenoid cystic carcinoma (SACC) patients with local invasion and lung metastasis are often resistant to conventional therapy such as operation, chemotherapy and radiotherapy. To explore the underling mechanisms, we studied the roles of miRNA in regulating invasiveness of SACC ce...

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Autores principales: Sun, Lijuan, Liu, Bodu, Lin, Zhaoyu, Yao, Yandan, Chen, Yanyang, Li, Yang, Chen, Jianing, Yu, Dongsheng, Tang, Zhangui, Wang, Bosheng, Zeng, Shuguang, Fan, Song, Wang, Youyuan, Li, Yilin, Song, Erwei, Li, Jinsong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4423101/
https://www.ncbi.nlm.nih.gov/pubmed/25924850
http://dx.doi.org/10.1186/s12943-015-0344-y
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author Sun, Lijuan
Liu, Bodu
Lin, Zhaoyu
Yao, Yandan
Chen, Yanyang
Li, Yang
Chen, Jianing
Yu, Dongsheng
Tang, Zhangui
Wang, Bosheng
Zeng, Shuguang
Fan, Song
Wang, Youyuan
Li, Yilin
Song, Erwei
Li, Jinsong
author_facet Sun, Lijuan
Liu, Bodu
Lin, Zhaoyu
Yao, Yandan
Chen, Yanyang
Li, Yang
Chen, Jianing
Yu, Dongsheng
Tang, Zhangui
Wang, Bosheng
Zeng, Shuguang
Fan, Song
Wang, Youyuan
Li, Yilin
Song, Erwei
Li, Jinsong
author_sort Sun, Lijuan
collection PubMed
description BACKGROUND: Salivary Adenoid cystic carcinoma (SACC) patients with local invasion and lung metastasis are often resistant to conventional therapy such as operation, chemotherapy and radiotherapy. To explore the underling mechanisms, we studied the roles of miRNA in regulating invasiveness of SACC cells. METHODS: MicroRNA profiling was done in SACC cells with microarray. MiRNA mimics or antisense oligonucleotide was transfected and invasiveness of SACC cells was evaluated by adhesion assay and transwell assay. The target gene of miRNA was identified by luciferase reporter assay and “rescue” experiment. Tumor metastasis was evaluated by BALB/c-nu mice xenografts. MiRNA and its target gene expression were identified by in-situ hybridization and immunohistochemistry respectively, in 302 patients from affiliated hospitals of Sun Yat-sen University and in 148 patients from affiliated hospitals of Central South University, and correlated to the clinicopathological status of the patients. RESULTS: MiR-320a was down-regulated in high lung metastatic ACCM and SACC-LM cells compared with the corresponding low metastatic ACC2 and SACC-83 cells, and inhibited adhesion, invasion and migration of SACC cells by targeting integrin beta 3 (ITGB3). In vivo, enforced miR-320a expression suppressed metastasis of SACC xenografts. In the two independent sets, miR-320a was downregulated in primary SACCs with metastasis compared to those without metastasis, and low expression of this miRNA predicts poor patient survival and rapid metastasis. Multivariate analysis showed that miR-320a expression was an independent indicator of lung metastasis. CONCLUSIONS: MiR-320a inhibits metastasis in SACCs by targeting ITGB3 and may serve as a therapeutic target and prognostic marker in salivary cancers. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12943-015-0344-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-44231012015-05-08 MiR-320a acts as a prognostic factor and Inhibits metastasis of salivary adenoid cystic carcinoma by targeting ITGB3 Sun, Lijuan Liu, Bodu Lin, Zhaoyu Yao, Yandan Chen, Yanyang Li, Yang Chen, Jianing Yu, Dongsheng Tang, Zhangui Wang, Bosheng Zeng, Shuguang Fan, Song Wang, Youyuan Li, Yilin Song, Erwei Li, Jinsong Mol Cancer Research BACKGROUND: Salivary Adenoid cystic carcinoma (SACC) patients with local invasion and lung metastasis are often resistant to conventional therapy such as operation, chemotherapy and radiotherapy. To explore the underling mechanisms, we studied the roles of miRNA in regulating invasiveness of SACC cells. METHODS: MicroRNA profiling was done in SACC cells with microarray. MiRNA mimics or antisense oligonucleotide was transfected and invasiveness of SACC cells was evaluated by adhesion assay and transwell assay. The target gene of miRNA was identified by luciferase reporter assay and “rescue” experiment. Tumor metastasis was evaluated by BALB/c-nu mice xenografts. MiRNA and its target gene expression were identified by in-situ hybridization and immunohistochemistry respectively, in 302 patients from affiliated hospitals of Sun Yat-sen University and in 148 patients from affiliated hospitals of Central South University, and correlated to the clinicopathological status of the patients. RESULTS: MiR-320a was down-regulated in high lung metastatic ACCM and SACC-LM cells compared with the corresponding low metastatic ACC2 and SACC-83 cells, and inhibited adhesion, invasion and migration of SACC cells by targeting integrin beta 3 (ITGB3). In vivo, enforced miR-320a expression suppressed metastasis of SACC xenografts. In the two independent sets, miR-320a was downregulated in primary SACCs with metastasis compared to those without metastasis, and low expression of this miRNA predicts poor patient survival and rapid metastasis. Multivariate analysis showed that miR-320a expression was an independent indicator of lung metastasis. CONCLUSIONS: MiR-320a inhibits metastasis in SACCs by targeting ITGB3 and may serve as a therapeutic target and prognostic marker in salivary cancers. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12943-015-0344-y) contains supplementary material, which is available to authorized users. BioMed Central 2015-04-29 /pmc/articles/PMC4423101/ /pubmed/25924850 http://dx.doi.org/10.1186/s12943-015-0344-y Text en © Sun et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Sun, Lijuan
Liu, Bodu
Lin, Zhaoyu
Yao, Yandan
Chen, Yanyang
Li, Yang
Chen, Jianing
Yu, Dongsheng
Tang, Zhangui
Wang, Bosheng
Zeng, Shuguang
Fan, Song
Wang, Youyuan
Li, Yilin
Song, Erwei
Li, Jinsong
MiR-320a acts as a prognostic factor and Inhibits metastasis of salivary adenoid cystic carcinoma by targeting ITGB3
title MiR-320a acts as a prognostic factor and Inhibits metastasis of salivary adenoid cystic carcinoma by targeting ITGB3
title_full MiR-320a acts as a prognostic factor and Inhibits metastasis of salivary adenoid cystic carcinoma by targeting ITGB3
title_fullStr MiR-320a acts as a prognostic factor and Inhibits metastasis of salivary adenoid cystic carcinoma by targeting ITGB3
title_full_unstemmed MiR-320a acts as a prognostic factor and Inhibits metastasis of salivary adenoid cystic carcinoma by targeting ITGB3
title_short MiR-320a acts as a prognostic factor and Inhibits metastasis of salivary adenoid cystic carcinoma by targeting ITGB3
title_sort mir-320a acts as a prognostic factor and inhibits metastasis of salivary adenoid cystic carcinoma by targeting itgb3
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4423101/
https://www.ncbi.nlm.nih.gov/pubmed/25924850
http://dx.doi.org/10.1186/s12943-015-0344-y
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