Long non-coding RNA (lncRNA) five prime to Xist (FTX) promotes retinoblastoma progression by regulating the microRNA-320a/with-nolysine kinases 1 (WNK1) axis: Running Head: LncRNA FTX promotes retinoblastoma

Long non-coding RNA (lncRNA) five prime to Xist (FTX) exerts important functions in human cancer, while its role in retinoblastoma (RB) remains unclear. This study aimed to investigate the role of FTX in RB. The expression levels of FTX were assessed by quantitative real-time polymerase chain reacti...

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Autores principales: Xiaolei Wang, Yu Su, Chuangao Yin
Formato: article
Lenguaje:EN
Publicado: Taylor & Francis Group 2021
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spelling oai:doaj.org-article:cf663bf1365646128fe1d44c9f7d498e2021-11-04T15:51:54ZLong non-coding RNA (lncRNA) five prime to Xist (FTX) promotes retinoblastoma progression by regulating the microRNA-320a/with-nolysine kinases 1 (WNK1) axis: Running Head: LncRNA FTX promotes retinoblastoma2165-59792165-598710.1080/21655979.2021.1994718https://doaj.org/article/cf663bf1365646128fe1d44c9f7d498e2021-11-01T00:00:00Zhttp://dx.doi.org/10.1080/21655979.2021.1994718https://doaj.org/toc/2165-5979https://doaj.org/toc/2165-5987Long non-coding RNA (lncRNA) five prime to Xist (FTX) exerts important functions in human cancer, while its role in retinoblastoma (RB) remains unclear. This study aimed to investigate the role of FTX in RB. The expression levels of FTX were assessed by quantitative real-time polymerase chain reaction (qRT-PCR). Cell proliferation was evaluated by cell counting kit-8 (CCK-8), 5‐ethynyl‐2′‐deoxyuridine (EdU) staining and colony formation assays. Cell migration and invasion were detected by Transwell assay. The relationship among FTX, microRNA-320a (miR-320a) and with-no lysine kinase 1 (WNK1) was also investigated. In the present study, we found that the expression levels of FTX were notably elevated in RB tissues and cancer cell lines. Overexpression of FTX exacerbated the aggressive phenotypes (cell proliferation, migration and invasion) of RB cells. Downregulation of miR-320a obviously attenuated the inhibitory effects of knockdown of FTX in RB malignant phenotypes, and knockdown of WNK1 also reversed the impacts of miR-320a inhibitor on malignant phenotypes. In vivo experiments further confirmed that knockdown of FTX efficiently prevent tumor growth in vivo. Our results revealed that FTX promoted RB progression by targeting the miR-320a/WNK1 axis (graphical abstract), suggesting that FTX might be a novel therapeutic target for RB.Xiaolei WangYu SuChuangao YinTaylor & Francis Grouparticleretinoblastomaftxmir-320awnk1BiotechnologyTP248.13-248.65ENBioengineered, Vol 0, Iss 0 (2021)
institution DOAJ
collection DOAJ
language EN
topic retinoblastoma
ftx
mir-320a
wnk1
Biotechnology
TP248.13-248.65
spellingShingle retinoblastoma
ftx
mir-320a
wnk1
Biotechnology
TP248.13-248.65
Xiaolei Wang
Yu Su
Chuangao Yin
Long non-coding RNA (lncRNA) five prime to Xist (FTX) promotes retinoblastoma progression by regulating the microRNA-320a/with-nolysine kinases 1 (WNK1) axis: Running Head: LncRNA FTX promotes retinoblastoma
description Long non-coding RNA (lncRNA) five prime to Xist (FTX) exerts important functions in human cancer, while its role in retinoblastoma (RB) remains unclear. This study aimed to investigate the role of FTX in RB. The expression levels of FTX were assessed by quantitative real-time polymerase chain reaction (qRT-PCR). Cell proliferation was evaluated by cell counting kit-8 (CCK-8), 5‐ethynyl‐2′‐deoxyuridine (EdU) staining and colony formation assays. Cell migration and invasion were detected by Transwell assay. The relationship among FTX, microRNA-320a (miR-320a) and with-no lysine kinase 1 (WNK1) was also investigated. In the present study, we found that the expression levels of FTX were notably elevated in RB tissues and cancer cell lines. Overexpression of FTX exacerbated the aggressive phenotypes (cell proliferation, migration and invasion) of RB cells. Downregulation of miR-320a obviously attenuated the inhibitory effects of knockdown of FTX in RB malignant phenotypes, and knockdown of WNK1 also reversed the impacts of miR-320a inhibitor on malignant phenotypes. In vivo experiments further confirmed that knockdown of FTX efficiently prevent tumor growth in vivo. Our results revealed that FTX promoted RB progression by targeting the miR-320a/WNK1 axis (graphical abstract), suggesting that FTX might be a novel therapeutic target for RB.
format article
author Xiaolei Wang
Yu Su
Chuangao Yin
author_facet Xiaolei Wang
Yu Su
Chuangao Yin
author_sort Xiaolei Wang
title Long non-coding RNA (lncRNA) five prime to Xist (FTX) promotes retinoblastoma progression by regulating the microRNA-320a/with-nolysine kinases 1 (WNK1) axis: Running Head: LncRNA FTX promotes retinoblastoma
title_short Long non-coding RNA (lncRNA) five prime to Xist (FTX) promotes retinoblastoma progression by regulating the microRNA-320a/with-nolysine kinases 1 (WNK1) axis: Running Head: LncRNA FTX promotes retinoblastoma
title_full Long non-coding RNA (lncRNA) five prime to Xist (FTX) promotes retinoblastoma progression by regulating the microRNA-320a/with-nolysine kinases 1 (WNK1) axis: Running Head: LncRNA FTX promotes retinoblastoma
title_fullStr Long non-coding RNA (lncRNA) five prime to Xist (FTX) promotes retinoblastoma progression by regulating the microRNA-320a/with-nolysine kinases 1 (WNK1) axis: Running Head: LncRNA FTX promotes retinoblastoma
title_full_unstemmed Long non-coding RNA (lncRNA) five prime to Xist (FTX) promotes retinoblastoma progression by regulating the microRNA-320a/with-nolysine kinases 1 (WNK1) axis: Running Head: LncRNA FTX promotes retinoblastoma
title_sort long non-coding rna (lncrna) five prime to xist (ftx) promotes retinoblastoma progression by regulating the microrna-320a/with-nolysine kinases 1 (wnk1) axis: running head: lncrna ftx promotes retinoblastoma
publisher Taylor & Francis Group
publishDate 2021
url https://doaj.org/article/cf663bf1365646128fe1d44c9f7d498e
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AT yusu longnoncodingrnalncrnafiveprimetoxistftxpromotesretinoblastomaprogressionbyregulatingthemicrorna320awithnolysinekinases1wnk1axisrunningheadlncrnaftxpromotesretinoblastoma
AT chuangaoyin longnoncodingrnalncrnafiveprimetoxistftxpromotesretinoblastomaprogressionbyregulatingthemicrorna320awithnolysinekinases1wnk1axisrunningheadlncrnaftxpromotesretinoblastoma
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