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. 2022 Apr 17;13(4):10112–10123. doi: 10.1080/21655979.2022.2063664

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© 2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Figure 3. — CircDLST served as a sponge for miR-489-3p. (a). The conjoint miRNAs of circDLST were predicted. (B) The miR-489-3p content in GC cells was detected by qRT-PCR. (c and d) The relationship between circDLST and miR-489-3p was assessed. (e and f) RIP assay was utilized to authenticate the link between circDLST and miR-489-3p. (g) RNA pull-down assay was adopted to confirm the link between circDLST and miR-489-3p. (h-j) The content of miR-489-3p in GC cells was uncovered by qRT-PCR. **P < 0.01, ***P < 0.001.