lncRNA MALAT1 regulated ATAD2 to facilitate retinoblastoma progression via miR-655-3p

Long noncoding RNA (lncRNA) metastasis-associated lung adenocarcinoma transcript 1 (MALAT1) was reported as an oncogene in many tumors including retinoblastoma (RB). This research mainly focused on the functions and mechanism of MALAT1 in RB. MALAT1 was upregulated in RB tissues and cells, and it se...

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Autores principales: Zhao Yuxin, Wang Zhaoxia, Gao Meili, Wang Xuehong, Feng Hui, Cui Yuanyuan, Tian Xia
Formato: article
Lenguaje:EN
Publicado: De Gruyter 2021
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Acceso en línea:https://doaj.org/article/1ba14620e00d496990f47fbc8b59bbea
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spelling oai:doaj.org-article:1ba14620e00d496990f47fbc8b59bbea2021-12-05T14:10:54ZlncRNA MALAT1 regulated ATAD2 to facilitate retinoblastoma progression via miR-655-3p2391-546310.1515/med-2021-0290https://doaj.org/article/1ba14620e00d496990f47fbc8b59bbea2021-06-01T00:00:00Zhttps://doi.org/10.1515/med-2021-0290https://doaj.org/toc/2391-5463Long noncoding RNA (lncRNA) metastasis-associated lung adenocarcinoma transcript 1 (MALAT1) was reported as an oncogene in many tumors including retinoblastoma (RB). This research mainly focused on the functions and mechanism of MALAT1 in RB. MALAT1 was upregulated in RB tissues and cells, and it served as a competing endogenous RNA (ceRNA) and inhibited miRNA-655-3p (miR-655-3p) expression, which eventually regulated the expression of miR-655-3p downstream target ATPase Family AAA Domain Containing 2 (ATAD2). The level of ATAD2 significantly increased, while that of miR-655-3p remarkably decreased in RB tissues and cells. MALAT1 depletion inhibited cell proliferation, metastasis, and epithelial–mesenchymal transition (EMT), but promoted apoptosis in vitro and blocked xenograft tumor growth in vivo. MALAT1 exerted its oncogenic functions in RB by regulating miR-655-3p/ATAD2 axis.Zhao YuxinWang ZhaoxiaGao MeiliWang XuehongFeng HuiCui YuanyuanTian XiaDe Gruyterarticlemalat1mir-655-3patad2tumor progressionretinoblastomaMedicineRENOpen Medicine, Vol 16, Iss 1, Pp 931-943 (2021)
institution DOAJ
collection DOAJ
language EN
topic malat1
mir-655-3p
atad2
tumor progression
retinoblastoma
Medicine
R
spellingShingle malat1
mir-655-3p
atad2
tumor progression
retinoblastoma
Medicine
R
Zhao Yuxin
Wang Zhaoxia
Gao Meili
Wang Xuehong
Feng Hui
Cui Yuanyuan
Tian Xia
lncRNA MALAT1 regulated ATAD2 to facilitate retinoblastoma progression via miR-655-3p
description Long noncoding RNA (lncRNA) metastasis-associated lung adenocarcinoma transcript 1 (MALAT1) was reported as an oncogene in many tumors including retinoblastoma (RB). This research mainly focused on the functions and mechanism of MALAT1 in RB. MALAT1 was upregulated in RB tissues and cells, and it served as a competing endogenous RNA (ceRNA) and inhibited miRNA-655-3p (miR-655-3p) expression, which eventually regulated the expression of miR-655-3p downstream target ATPase Family AAA Domain Containing 2 (ATAD2). The level of ATAD2 significantly increased, while that of miR-655-3p remarkably decreased in RB tissues and cells. MALAT1 depletion inhibited cell proliferation, metastasis, and epithelial–mesenchymal transition (EMT), but promoted apoptosis in vitro and blocked xenograft tumor growth in vivo. MALAT1 exerted its oncogenic functions in RB by regulating miR-655-3p/ATAD2 axis.
format article
author Zhao Yuxin
Wang Zhaoxia
Gao Meili
Wang Xuehong
Feng Hui
Cui Yuanyuan
Tian Xia
author_facet Zhao Yuxin
Wang Zhaoxia
Gao Meili
Wang Xuehong
Feng Hui
Cui Yuanyuan
Tian Xia
author_sort Zhao Yuxin
title lncRNA MALAT1 regulated ATAD2 to facilitate retinoblastoma progression via miR-655-3p
title_short lncRNA MALAT1 regulated ATAD2 to facilitate retinoblastoma progression via miR-655-3p
title_full lncRNA MALAT1 regulated ATAD2 to facilitate retinoblastoma progression via miR-655-3p
title_fullStr lncRNA MALAT1 regulated ATAD2 to facilitate retinoblastoma progression via miR-655-3p
title_full_unstemmed lncRNA MALAT1 regulated ATAD2 to facilitate retinoblastoma progression via miR-655-3p
title_sort lncrna malat1 regulated atad2 to facilitate retinoblastoma progression via mir-655-3p
publisher De Gruyter
publishDate 2021
url https://doaj.org/article/1ba14620e00d496990f47fbc8b59bbea
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AT gaomeili lncrnamalat1regulatedatad2tofacilitateretinoblastomaprogressionviamir6553p
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