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. 2019 Mar 22;9:28. doi: 10.1186/s13578-019-0290-2

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© The Author(s) 2019

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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Fig. 2 — SNHG7 knockdown suppressed PC cell proliferation, migration and invasion in vitro. After transfection with siRNA of SNHG7 or negative control (NC) into PANC-1 and PaCa-2 cell lines, a the expression level of SNHG7 was measured by RT-qPCR; b cell viability was determined by CCK-8 assay; c the apoptotic rate was measured by flow cytometric; d cell migration rate was analyzed by wound healing assay; e cell invasion was determined by transwell assay. *P < 0.1, **P < 0.01, compared with si-NC group