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LncRNA NBR2 suppresses migration and invasion of colorectal cancer cells by downregulating miRNA-21

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Abstract

It has been reported that lncRNA NBR2 regulates cancer metabolism. We investigated the role of NBR2 in colorectal cancer. We found that NBR2 was downregulated in colorectal cancer tissues than in adjacent healthy tissues. Decreased expression levels of NBR2 in tumor tissues were observed with the increase of clinical stages. MiRNA-21 was upregulated in colorectal cancer tissues than in adjacent healthy tissues, and was significantly and inversely correlated with NBR2. NBR2 overexpression downregulated miRNA-21 in colorectal cancer cells, while miRNA-21 overexpression failed to significantly affect NBR2 expression. NBR2 overexpression suppressed migration and invasion of colorectal cancer cells. MiRNA-21 overexpression played an opposite role and attenuated the effects of NBR2 overexpression. NBR2 overexpression did not significantly alter cancer cell proliferation. Therefore, lncRNA NBR2 inhibited colorectal cancer cell migration and invasion possibly by downregulating miRNA-21.

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Acknowledgements

We thank the financial support from the National Natural Science Fund from the National Natural Science Foundation of China (Grant nos. 81672427)

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Rui Zhang analyzed data and drafted manuscript. Jinghui Bai, Jian Xu and Jian Zhao performed experiments and collected data.

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Correspondence to Rui Zhang.

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This research was approved by Ethics Committee of Cancer Hospital of China Medical University, Liaoning Cancer Hospital & Institute.

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Expression levels of miRNA-21 in patients at different clinical stages (JPG 141 kb)

13577_2019_265_MOESM2_ESM.jpg

Luciferase activity assay revealed that the interaction between NBR2 and miRNA-21 is indirect. Luciferase activity assay was performed to analyze the interaction between NBR2 and miRNA-21 in RKO (A) and HT115 (B) cells (JPG 181 kb)

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Bai, J., Xu, J., Zhao, J. et al. LncRNA NBR2 suppresses migration and invasion of colorectal cancer cells by downregulating miRNA-21. Human Cell 33, 98–103 (2020). https://doi.org/10.1007/s13577-019-00265-1

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  • DOI: https://doi.org/10.1007/s13577-019-00265-1

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