Please use this identifier to cite or link to this item: https://doi.org/10.2147/CMAR.S207084
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dc.titleLong noncoding RNA Linc00460 promotes breast cancer progression by regulating the miR-489-5p/FGF7/AKT axis
dc.contributor.authorZhu, Y.
dc.contributor.authorYang, L.
dc.contributor.authorChong, Q.-Y.
dc.contributor.authorYan, H.
dc.contributor.authorZhang, W.
dc.contributor.authorQian, W.
dc.contributor.authorTan, S.
dc.contributor.authorWu, Z.
dc.contributor.authorLobie, P.E.
dc.contributor.authorZhu, T.
dc.date.accessioned2022-01-19T04:12:35Z
dc.date.available2022-01-19T04:12:35Z
dc.date.issued2019
dc.identifier.citationZhu, Y., Yang, L., Chong, Q.-Y., Yan, H., Zhang, W., Qian, W., Tan, S., Wu, Z., Lobie, P.E., Zhu, T. (2019). Long noncoding RNA Linc00460 promotes breast cancer progression by regulating the miR-489-5p/FGF7/AKT axis. Cancer Management and Research 11 : 5983-6001. ScholarBank@NUS Repository. https://doi.org/10.2147/CMAR.S207084
dc.identifier.issn11791322
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/214000
dc.description.abstractPurpose: Evidence indicates that long noncoding RNAs (lncRNA) possess important roles in various cellular processes and that dysregulation of lncRNAs promotes tumor progression. However, the expression patterns and biological functions of many specific lncRNAs in breast cancer remain to be determined. Methods: Quantitative real-time polymerase chain reaction was performed to detect Linc00460, miR-489-5p and FGF7 expression. Protein levels were determined using Western blot. MTT and colony formation assay were used to measure cell proliferation. Transwell assays were conducted to determine cell migration and invasion. Luciferase reporter assays were carried out to assess the interaction between miR-489-5p and Linc00460 or FGF7. Biotin pull-down assay was used to detect the direct interaction between miR-489-5p and Linc00460. In vivo experiments were performed to measure tumor formation and lung metastasis. Results: We demonstrated that lncRNA Linc00460 was upregulated in breast cancer, and its expression level was positively associated with lymphatic metastasis and poor overall survival. Forced expression of Linc00460 increased, whereas Linc00460 silencing decreased, breast cancer cell viability, migration and invasion both in vitro and in vivo. Linc00460 was identified as a direct target of miR-489-5p, which further targeted FGF7 and exerted oncogenic functions in breast cancer. Mechanistically, Linc00460 served as a competing endogenous RNA of FGF-7 mRNA by sponging miR-489-5p, resulting in upregulated FGF7 expression and AKT activity. Notably, forced expression of miR-489-5p abrogated Linc00460-mediated oncogenic behavior and activation of the FGF7-AKT pathway in breast cancer cells. Conclusion: We have demonstrated that Linc00460 promotes breast cancer progression partly through the miR-489-5p/FGF7/AKT axis. � 2019 Zhu et al.
dc.publisherDove Medical Press Ltd
dc.rightsAttribution-NonCommercial 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by-nc/4.0/
dc.sourceScopus OA2019
dc.subjectAKT
dc.subjectBreast cancer
dc.subjectFGF7
dc.subjectLinc00460
dc.subjectMiR-489-5p
dc.typeArticle
dc.contributor.departmentCANCER SCIENCE INSTITUTE OF SINGAPORE
dc.description.doi10.2147/CMAR.S207084
dc.description.sourcetitleCancer Management and Research
dc.description.volume11
dc.description.page5983-6001
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