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LncRNA LINC00665 Promotes Prostate Cancer Progression via miR-1224-5p/SND1 Axis

BACKGROUND: Increasing researches have revealed a critical role of long noncoding RNAs (lncRNAs) in tumor progression. LINC00665 is a poorly investigated lncRNA. In this research, we sought to determine the potential role of LINC00665 in prostate cancer (PC) progression. METHODS: LINC00665 expressio...

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Autores principales: Chen, Wei, Yu, Zhixian, Huang, Weiping, Yang, Yu, Wang, Feng, Huang, Hang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7105362/
https://www.ncbi.nlm.nih.gov/pubmed/32273723
http://dx.doi.org/10.2147/OTT.S241578
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author Chen, Wei
Yu, Zhixian
Huang, Weiping
Yang, Yu
Wang, Feng
Huang, Hang
author_facet Chen, Wei
Yu, Zhixian
Huang, Weiping
Yang, Yu
Wang, Feng
Huang, Hang
author_sort Chen, Wei
collection PubMed
description BACKGROUND: Increasing researches have revealed a critical role of long noncoding RNAs (lncRNAs) in tumor progression. LINC00665 is a poorly investigated lncRNA. In this research, we sought to determine the potential role of LINC00665 in prostate cancer (PC) progression. METHODS: LINC00665 expression was analyzed by bioinformatics method and qRT-PCR. Proliferation was determined via CCK8 and colony formation assays. Transwell assay was conducted to analyze migration and invasion. Xenograft assay was used to test the roles of LINC00665 in vivo. Luciferase reporter assay, pulldown assay and RIP assay were utilized to confirm the interaction between LINC00665 and miR-1224-5p. RESULTS: LINC00665 expression was increased in PC samples in contrast to control tissues, according to bioinformatics analysis and qRT-PCR validation. LINC00665 high expression was related to a poor prognosis. LINC00665 knockdown markedly attenuated growth and metastasis of PC cells and impaired tumor propagation in vivo. Mechanistic investigation revealed that LINC00665 was the sponge for miR-1224-5p. By inhibiting miR-1224-5p level, LINC00665 dramatically promoted the expression of SND1 in PC cells. Ectopic expression of SND1 significantly rescued the effects of LINC00665 silencing. CONCLUSION: LINC00665 is a novel oncogenic gene in PC by targeting miR-1224-5p/SND1 pathway and may be a therapeutic target.
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spelling pubmed-71053622020-04-09 LncRNA LINC00665 Promotes Prostate Cancer Progression via miR-1224-5p/SND1 Axis Chen, Wei Yu, Zhixian Huang, Weiping Yang, Yu Wang, Feng Huang, Hang Onco Targets Ther Original Research BACKGROUND: Increasing researches have revealed a critical role of long noncoding RNAs (lncRNAs) in tumor progression. LINC00665 is a poorly investigated lncRNA. In this research, we sought to determine the potential role of LINC00665 in prostate cancer (PC) progression. METHODS: LINC00665 expression was analyzed by bioinformatics method and qRT-PCR. Proliferation was determined via CCK8 and colony formation assays. Transwell assay was conducted to analyze migration and invasion. Xenograft assay was used to test the roles of LINC00665 in vivo. Luciferase reporter assay, pulldown assay and RIP assay were utilized to confirm the interaction between LINC00665 and miR-1224-5p. RESULTS: LINC00665 expression was increased in PC samples in contrast to control tissues, according to bioinformatics analysis and qRT-PCR validation. LINC00665 high expression was related to a poor prognosis. LINC00665 knockdown markedly attenuated growth and metastasis of PC cells and impaired tumor propagation in vivo. Mechanistic investigation revealed that LINC00665 was the sponge for miR-1224-5p. By inhibiting miR-1224-5p level, LINC00665 dramatically promoted the expression of SND1 in PC cells. Ectopic expression of SND1 significantly rescued the effects of LINC00665 silencing. CONCLUSION: LINC00665 is a novel oncogenic gene in PC by targeting miR-1224-5p/SND1 pathway and may be a therapeutic target. Dove 2020-03-26 /pmc/articles/PMC7105362/ /pubmed/32273723 http://dx.doi.org/10.2147/OTT.S241578 Text en © 2020 Chen et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Chen, Wei
Yu, Zhixian
Huang, Weiping
Yang, Yu
Wang, Feng
Huang, Hang
LncRNA LINC00665 Promotes Prostate Cancer Progression via miR-1224-5p/SND1 Axis
title LncRNA LINC00665 Promotes Prostate Cancer Progression via miR-1224-5p/SND1 Axis
title_full LncRNA LINC00665 Promotes Prostate Cancer Progression via miR-1224-5p/SND1 Axis
title_fullStr LncRNA LINC00665 Promotes Prostate Cancer Progression via miR-1224-5p/SND1 Axis
title_full_unstemmed LncRNA LINC00665 Promotes Prostate Cancer Progression via miR-1224-5p/SND1 Axis
title_short LncRNA LINC00665 Promotes Prostate Cancer Progression via miR-1224-5p/SND1 Axis
title_sort lncrna linc00665 promotes prostate cancer progression via mir-1224-5p/snd1 axis
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7105362/
https://www.ncbi.nlm.nih.gov/pubmed/32273723
http://dx.doi.org/10.2147/OTT.S241578
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