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RNU12 inhibits gastric cancer progression via sponging miR-575 and targeting BLID

Gastric cancer (GC) is one of the major causes of cancer deaths with 5-year survival ratio of 20%. RNU12 is one of long noncoding RNAs (lncRNAs) regulating the tumor progression. However, how RNU12 affecting GC is not clear. qRT-PCR was utilized for determining the RNU12 expression in cell lines, 11...

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Autores principales: Wang, Shaoli, Zou, Changyan, Lin, Xinyi, Hu, Dan, Su, Ying, He, Huocong, Zheng, Xiongwei, Zhang, Lurong, Huang, Tao, Liao, Jin-rong, Lin, Xiandong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10169768/
https://www.ncbi.nlm.nih.gov/pubmed/37160927
http://dx.doi.org/10.1038/s41598-023-34539-4
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author Wang, Shaoli
Zou, Changyan
Lin, Xinyi
Hu, Dan
Su, Ying
He, Huocong
Zheng, Xiongwei
Zhang, Lurong
Huang, Tao
Liao, Jin-rong
Lin, Xiandong
author_facet Wang, Shaoli
Zou, Changyan
Lin, Xinyi
Hu, Dan
Su, Ying
He, Huocong
Zheng, Xiongwei
Zhang, Lurong
Huang, Tao
Liao, Jin-rong
Lin, Xiandong
author_sort Wang, Shaoli
collection PubMed
description Gastric cancer (GC) is one of the major causes of cancer deaths with 5-year survival ratio of 20%. RNU12 is one of long noncoding RNAs (lncRNAs) regulating the tumor progression. However, how RNU12 affecting GC is not clear. qRT-PCR was utilized for determining the RNU12 expression in cell lines, 113 cases of paired gastric cancer (GC) and their adjacent normal gastric tissues. The biofunction alterations of RNU12 were assessed by its overexpression or knockdown in GC cells. MTT and cloning assay were assayed for the cell proliferation, the flow cytometry for the detection of cell cycle and the wound healing assay (WHA) and transwell invasion assay (TIA) for examining the migration and invasion of cells. The expressions of a set of genes related proliferation and migration were investigated with the Western Blotting (WB). RNA immunoprecipitation (RIP), biotinylated RNA pull-down and dual luciferase reporter tests were used to detect the interactions of RNU12 with miR-575/BLID. The in vivo proliferation and migration ability of RNU12 infected cells were determined in zebrafish system. This study revealed that RNU12 inhibited proliferation, invasion and metastasis by sponging of miR-575 and regulating the downstream BLID and modulated EMT of GC cells. The RNU12/miR-575/BLID axis is likely to be the prognosis biomarkers and drug targets of GC.
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spelling pubmed-101697682023-05-11 RNU12 inhibits gastric cancer progression via sponging miR-575 and targeting BLID Wang, Shaoli Zou, Changyan Lin, Xinyi Hu, Dan Su, Ying He, Huocong Zheng, Xiongwei Zhang, Lurong Huang, Tao Liao, Jin-rong Lin, Xiandong Sci Rep Article Gastric cancer (GC) is one of the major causes of cancer deaths with 5-year survival ratio of 20%. RNU12 is one of long noncoding RNAs (lncRNAs) regulating the tumor progression. However, how RNU12 affecting GC is not clear. qRT-PCR was utilized for determining the RNU12 expression in cell lines, 113 cases of paired gastric cancer (GC) and their adjacent normal gastric tissues. The biofunction alterations of RNU12 were assessed by its overexpression or knockdown in GC cells. MTT and cloning assay were assayed for the cell proliferation, the flow cytometry for the detection of cell cycle and the wound healing assay (WHA) and transwell invasion assay (TIA) for examining the migration and invasion of cells. The expressions of a set of genes related proliferation and migration were investigated with the Western Blotting (WB). RNA immunoprecipitation (RIP), biotinylated RNA pull-down and dual luciferase reporter tests were used to detect the interactions of RNU12 with miR-575/BLID. The in vivo proliferation and migration ability of RNU12 infected cells were determined in zebrafish system. This study revealed that RNU12 inhibited proliferation, invasion and metastasis by sponging of miR-575 and regulating the downstream BLID and modulated EMT of GC cells. The RNU12/miR-575/BLID axis is likely to be the prognosis biomarkers and drug targets of GC. Nature Publishing Group UK 2023-05-09 /pmc/articles/PMC10169768/ /pubmed/37160927 http://dx.doi.org/10.1038/s41598-023-34539-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Wang, Shaoli
Zou, Changyan
Lin, Xinyi
Hu, Dan
Su, Ying
He, Huocong
Zheng, Xiongwei
Zhang, Lurong
Huang, Tao
Liao, Jin-rong
Lin, Xiandong
RNU12 inhibits gastric cancer progression via sponging miR-575 and targeting BLID
title RNU12 inhibits gastric cancer progression via sponging miR-575 and targeting BLID
title_full RNU12 inhibits gastric cancer progression via sponging miR-575 and targeting BLID
title_fullStr RNU12 inhibits gastric cancer progression via sponging miR-575 and targeting BLID
title_full_unstemmed RNU12 inhibits gastric cancer progression via sponging miR-575 and targeting BLID
title_short RNU12 inhibits gastric cancer progression via sponging miR-575 and targeting BLID
title_sort rnu12 inhibits gastric cancer progression via sponging mir-575 and targeting blid
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10169768/
https://www.ncbi.nlm.nih.gov/pubmed/37160927
http://dx.doi.org/10.1038/s41598-023-34539-4
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