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lncRNA MNX1-AS1 Promotes Glioblastoma Progression Through Inhibition of miR-4443

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Department of Neurology, Shengjing Hospital, Affiliated Hospital of China Medical University, Shenyang, P.R. China

Oncology Research 2019, 27(3), 341-347. https://doi.org/10.3727/096504018X15228909735079

Abstract

Long noncoding RNAs (lncRNAs) have been acknowledged as important regulators in various human cancers. lncRNA MNX1-AS1 has been shown to be an oncogene in epithelial ovarian cancer. However, the function of MNX1-AS1 in glioblastoma (GBM) remains largely unknown. Here we found that the expression of MNX1-AS1 was significantly upregulated in GBM tissues and cell lines. Knockdown of MNX1-AS1 significantly inhibited the proliferation, migration, and invasion of GBM cells. In terms of mechanism, we found that MNX1-AS1 could bind to miR-4443 in GBM cells. Overexpression of miR-4443 significantly inhibited the expression of MNX1-AS1 and vice versa. Moreover, there was an inverse correlation between the expression levels of MNX1-AS1 and miR-4443 in GBM tissues. We found that overexpression of miR-4443 inhibited the proliferation, migration, and invasion of GBM cells. We also showed that inhibition of miR-4443 reversed the effects of MNX1-AS1 knockdown on GBM cell proliferation, migration, and invasion. Taken together, we found that MNX1-AS1 promoted the proliferation, migration, and invasion of GBM cells through inhibiting miR-4443.

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APA Style
Gao, Y., Xu, Y., Wang, J., Yang, X., Wen, L. et al. (2019). Lncrna MNX1-AS1 promotes glioblastoma progression through inhibition of mir-4443. Oncology Research, 27(3), 341-347. https://doi.org/10.3727/096504018X15228909735079
Vancouver Style
Gao Y, Xu Y, Wang J, Yang X, Wen L, Feng J. Lncrna MNX1-AS1 promotes glioblastoma progression through inhibition of mir-4443. Oncol Res. 2019;27(3):341-347 https://doi.org/10.3727/096504018X15228909735079
IEEE Style
Y. Gao, Y. Xu, J. Wang, X. Yang, L. Wen, and J. Feng, “lncRNA MNX1-AS1 Promotes Glioblastoma Progression Through Inhibition of miR-4443,” Oncol. Res., vol. 27, no. 3, pp. 341-347, 2019. https://doi.org/10.3727/096504018X15228909735079



cc Copyright © 2019 The Author(s). Published by Tech Science Press.
This work is licensed under a Creative Commons Attribution 4.0 International License , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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