Cargando…

LncRNA NEAT1 Promotes the Malignant Progression of Colorectal Cancer by Targeting ZEB1 via miR-448

Background: Long noncoding RNAs have been associated with various types of malignant tumors; however, the specific role of long noncoding RNAs in tumorigenesis still remains unclear in colorectal cancer. Here, we aim to elucidate the role of long noncoding RNA nuclear paraspeckle assembly transcript...

Descripción completa

Detalles Bibliográficos
Autores principales: Wu, Hanquan, Dong, Dengwen, Wang, Jiwei, Yin, Shiwen, Gong, Yuanxiang, Yang, Chao, Bai, Yihan, Wang, Junyi, Du, Yanhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9201302/
https://www.ncbi.nlm.nih.gov/pubmed/35695254
http://dx.doi.org/10.1177/15330338221085348
_version_ 1784728280299995136
author Wu, Hanquan
Dong, Dengwen
Wang, Jiwei
Yin, Shiwen
Gong, Yuanxiang
Yang, Chao
Bai, Yihan
Wang, Junyi
Du, Yanhong
author_facet Wu, Hanquan
Dong, Dengwen
Wang, Jiwei
Yin, Shiwen
Gong, Yuanxiang
Yang, Chao
Bai, Yihan
Wang, Junyi
Du, Yanhong
author_sort Wu, Hanquan
collection PubMed
description Background: Long noncoding RNAs have been associated with various types of malignant tumors; however, the specific role of long noncoding RNAs in tumorigenesis still remains unclear in colorectal cancer. Here, we aim to elucidate the role of long noncoding RNA nuclear paraspeckle assembly transcript 1 in the malignant progression of colorectal cancer and investigate its underlying mechanisms. Methods: Real-time polymerase chain reaction was used to detect the expression of nuclear paraspeckle assembly transcript 1 in colorectal cancer tissues and cells. Cell Counting Kit-8 assay was used to determine the effect of nuclear paraspeckle assembly transcript 1 in proliferation. Transwell assay was used to explore the role of nuclear paraspeckle assembly transcript 1 in metastasis. Bioinformatics method was used to predict the core nuclear paraspeckle assembly transcript 1 interaction network. Real-time polymerase chain reaction was used to detect nuclear paraspeckle assembly transcript 1 and miR-448 expression levels. Western blotting was used to detect the expression levels of ZEB1. Luciferase assay was used to verify the relationship among nuclear paraspeckle assembly transcript 1, miR-448, and ZEB1. The effect of nuclear paraspeckle assembly transcript 1 on tumor growth was detected by tumorigenesis test in nude mice. Results: Long noncoding RNA–nuclear paraspeckle assembly transcript 1 was up-regulated in colorectal cancer tissues and cells. Knocking down of nuclear paraspeckle assembly transcript 1 can suppress colorectal cancer proliferation and invasion, and caused a reduction of ZEB1 expression and an increase of miR-448 expression. Furthermore, knockdown of nuclear paraspeckle assembly transcript 1 regulated miR-448/ZEB1 axis to inhibit the expression of ZEB1. miR-448 silencing can reverse the effect of nuclear paraspeckle assembly transcript 1 knockdown. Conclusion: Our result demonstrated that long noncoding RNA nuclear paraspeckle assembly transcript 1 promotes proliferation and invasion of colorectal cancer by targeting miR-448 to promote the expression of ZEB1, which may play a significant role in the tumorigenesis of colorectal cancer.
format Online
Article
Text
id pubmed-9201302
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher SAGE Publications
record_format MEDLINE/PubMed
spelling pubmed-92013022022-06-17 LncRNA NEAT1 Promotes the Malignant Progression of Colorectal Cancer by Targeting ZEB1 via miR-448 Wu, Hanquan Dong, Dengwen Wang, Jiwei Yin, Shiwen Gong, Yuanxiang Yang, Chao Bai, Yihan Wang, Junyi Du, Yanhong Technol Cancer Res Treat Original Article Background: Long noncoding RNAs have been associated with various types of malignant tumors; however, the specific role of long noncoding RNAs in tumorigenesis still remains unclear in colorectal cancer. Here, we aim to elucidate the role of long noncoding RNA nuclear paraspeckle assembly transcript 1 in the malignant progression of colorectal cancer and investigate its underlying mechanisms. Methods: Real-time polymerase chain reaction was used to detect the expression of nuclear paraspeckle assembly transcript 1 in colorectal cancer tissues and cells. Cell Counting Kit-8 assay was used to determine the effect of nuclear paraspeckle assembly transcript 1 in proliferation. Transwell assay was used to explore the role of nuclear paraspeckle assembly transcript 1 in metastasis. Bioinformatics method was used to predict the core nuclear paraspeckle assembly transcript 1 interaction network. Real-time polymerase chain reaction was used to detect nuclear paraspeckle assembly transcript 1 and miR-448 expression levels. Western blotting was used to detect the expression levels of ZEB1. Luciferase assay was used to verify the relationship among nuclear paraspeckle assembly transcript 1, miR-448, and ZEB1. The effect of nuclear paraspeckle assembly transcript 1 on tumor growth was detected by tumorigenesis test in nude mice. Results: Long noncoding RNA–nuclear paraspeckle assembly transcript 1 was up-regulated in colorectal cancer tissues and cells. Knocking down of nuclear paraspeckle assembly transcript 1 can suppress colorectal cancer proliferation and invasion, and caused a reduction of ZEB1 expression and an increase of miR-448 expression. Furthermore, knockdown of nuclear paraspeckle assembly transcript 1 regulated miR-448/ZEB1 axis to inhibit the expression of ZEB1. miR-448 silencing can reverse the effect of nuclear paraspeckle assembly transcript 1 knockdown. Conclusion: Our result demonstrated that long noncoding RNA nuclear paraspeckle assembly transcript 1 promotes proliferation and invasion of colorectal cancer by targeting miR-448 to promote the expression of ZEB1, which may play a significant role in the tumorigenesis of colorectal cancer. SAGE Publications 2022-06-12 /pmc/articles/PMC9201302/ /pubmed/35695254 http://dx.doi.org/10.1177/15330338221085348 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Article
Wu, Hanquan
Dong, Dengwen
Wang, Jiwei
Yin, Shiwen
Gong, Yuanxiang
Yang, Chao
Bai, Yihan
Wang, Junyi
Du, Yanhong
LncRNA NEAT1 Promotes the Malignant Progression of Colorectal Cancer by Targeting ZEB1 via miR-448
title LncRNA NEAT1 Promotes the Malignant Progression of Colorectal Cancer by Targeting ZEB1 via miR-448
title_full LncRNA NEAT1 Promotes the Malignant Progression of Colorectal Cancer by Targeting ZEB1 via miR-448
title_fullStr LncRNA NEAT1 Promotes the Malignant Progression of Colorectal Cancer by Targeting ZEB1 via miR-448
title_full_unstemmed LncRNA NEAT1 Promotes the Malignant Progression of Colorectal Cancer by Targeting ZEB1 via miR-448
title_short LncRNA NEAT1 Promotes the Malignant Progression of Colorectal Cancer by Targeting ZEB1 via miR-448
title_sort lncrna neat1 promotes the malignant progression of colorectal cancer by targeting zeb1 via mir-448
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9201302/
https://www.ncbi.nlm.nih.gov/pubmed/35695254
http://dx.doi.org/10.1177/15330338221085348
work_keys_str_mv AT wuhanquan lncrnaneat1promotesthemalignantprogressionofcolorectalcancerbytargetingzeb1viamir448
AT dongdengwen lncrnaneat1promotesthemalignantprogressionofcolorectalcancerbytargetingzeb1viamir448
AT wangjiwei lncrnaneat1promotesthemalignantprogressionofcolorectalcancerbytargetingzeb1viamir448
AT yinshiwen lncrnaneat1promotesthemalignantprogressionofcolorectalcancerbytargetingzeb1viamir448
AT gongyuanxiang lncrnaneat1promotesthemalignantprogressionofcolorectalcancerbytargetingzeb1viamir448
AT yangchao lncrnaneat1promotesthemalignantprogressionofcolorectalcancerbytargetingzeb1viamir448
AT baiyihan lncrnaneat1promotesthemalignantprogressionofcolorectalcancerbytargetingzeb1viamir448
AT wangjunyi lncrnaneat1promotesthemalignantprogressionofcolorectalcancerbytargetingzeb1viamir448
AT duyanhong lncrnaneat1promotesthemalignantprogressionofcolorectalcancerbytargetingzeb1viamir448