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circNSUN2 promotes the malignant biological behavior of colorectal cancer cells via the miR-181a-5p/ROCK2 axis
Aberrant expression of circular RNAs (circRNAs) has been demonstrated to be related to the development of colorectal cancer (CRC), the third most common cancer worldwide. However, the mechanism of the effect of circRNA NOP2/Sun domain family, member 2 (circNSUN2) on the malignant biological behavior...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8165598/ https://www.ncbi.nlm.nih.gov/pubmed/34080658 http://dx.doi.org/10.3892/or.2021.8093 |
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author | Chi, Junlin Liu, Shuang Wu, Zhizhong Shi, Yanqiang Shi, Chengmin Zhang, Tong Xiong, Binghong Zeng, Yujian Dong, Xiangqian |
author_facet | Chi, Junlin Liu, Shuang Wu, Zhizhong Shi, Yanqiang Shi, Chengmin Zhang, Tong Xiong, Binghong Zeng, Yujian Dong, Xiangqian |
author_sort | Chi, Junlin |
collection | PubMed |
description | Aberrant expression of circular RNAs (circRNAs) has been demonstrated to be related to the development of colorectal cancer (CRC), the third most common cancer worldwide. However, the mechanism of the effect of circRNA NOP2/Sun domain family, member 2 (circNSUN2) on the malignant biological behavior of CRC remains unclear. In the present study, the expression of circNSUN2 and microRNA (miR)-181a-5p was detected by RT-qPCR. The expression of Rho-associated coiled-coil-containing protein kinase 2 (ROCK2) was measured by western blotting. Cell proliferation was detected by CCK-8 assay. The cell apoptosis rate was measured by flow cytometry. Cell migration ability was evaluated by Transwell assay. The interactions between circNSUN2, miR-181a-5p and ROCK2 were verified by dual-luciferase reporter assay. The results revealed that circNSUN2 was highly expressed in CRC tissues and cell lines. Knockdown of circNSUN2 inhibited the malignant biological behavior of CRC in vivo and in vitro. Moreover, miR-181a-5p was revealed to be a target gene of circNSUN2, and the expression of ROCK2 was negatively regulated by miR-181a-5p. Knockdown of circNSUN2 inhibited proliferation and migration, and induced apoptosis of CRC cells and suppressed tumor growth by targeting miR-181a-5p to decrease ROCK2 expression. In conclusion, circNSUN2 promoted the progression of CRC by sponging miR-181a-5p to increase the expression of ROCK2. |
format | Online Article Text |
id | pubmed-8165598 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-81655982021-06-03 circNSUN2 promotes the malignant biological behavior of colorectal cancer cells via the miR-181a-5p/ROCK2 axis Chi, Junlin Liu, Shuang Wu, Zhizhong Shi, Yanqiang Shi, Chengmin Zhang, Tong Xiong, Binghong Zeng, Yujian Dong, Xiangqian Oncol Rep Articles Aberrant expression of circular RNAs (circRNAs) has been demonstrated to be related to the development of colorectal cancer (CRC), the third most common cancer worldwide. However, the mechanism of the effect of circRNA NOP2/Sun domain family, member 2 (circNSUN2) on the malignant biological behavior of CRC remains unclear. In the present study, the expression of circNSUN2 and microRNA (miR)-181a-5p was detected by RT-qPCR. The expression of Rho-associated coiled-coil-containing protein kinase 2 (ROCK2) was measured by western blotting. Cell proliferation was detected by CCK-8 assay. The cell apoptosis rate was measured by flow cytometry. Cell migration ability was evaluated by Transwell assay. The interactions between circNSUN2, miR-181a-5p and ROCK2 were verified by dual-luciferase reporter assay. The results revealed that circNSUN2 was highly expressed in CRC tissues and cell lines. Knockdown of circNSUN2 inhibited the malignant biological behavior of CRC in vivo and in vitro. Moreover, miR-181a-5p was revealed to be a target gene of circNSUN2, and the expression of ROCK2 was negatively regulated by miR-181a-5p. Knockdown of circNSUN2 inhibited proliferation and migration, and induced apoptosis of CRC cells and suppressed tumor growth by targeting miR-181a-5p to decrease ROCK2 expression. In conclusion, circNSUN2 promoted the progression of CRC by sponging miR-181a-5p to increase the expression of ROCK2. D.A. Spandidos 2021-07 2021-05-27 /pmc/articles/PMC8165598/ /pubmed/34080658 http://dx.doi.org/10.3892/or.2021.8093 Text en Copyright: © Chi et al. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Chi, Junlin Liu, Shuang Wu, Zhizhong Shi, Yanqiang Shi, Chengmin Zhang, Tong Xiong, Binghong Zeng, Yujian Dong, Xiangqian circNSUN2 promotes the malignant biological behavior of colorectal cancer cells via the miR-181a-5p/ROCK2 axis |
title | circNSUN2 promotes the malignant biological behavior of colorectal cancer cells via the miR-181a-5p/ROCK2 axis |
title_full | circNSUN2 promotes the malignant biological behavior of colorectal cancer cells via the miR-181a-5p/ROCK2 axis |
title_fullStr | circNSUN2 promotes the malignant biological behavior of colorectal cancer cells via the miR-181a-5p/ROCK2 axis |
title_full_unstemmed | circNSUN2 promotes the malignant biological behavior of colorectal cancer cells via the miR-181a-5p/ROCK2 axis |
title_short | circNSUN2 promotes the malignant biological behavior of colorectal cancer cells via the miR-181a-5p/ROCK2 axis |
title_sort | circnsun2 promotes the malignant biological behavior of colorectal cancer cells via the mir-181a-5p/rock2 axis |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8165598/ https://www.ncbi.nlm.nih.gov/pubmed/34080658 http://dx.doi.org/10.3892/or.2021.8093 |
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