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. 2021 Dec 20;13(1):15. doi: 10.1038/s41419-021-04387-z

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© The Author(s) 2021

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 3 — a The qPCR-based expression levels of MYEOV in four types of stable PANC-1 cell lines. PANC-1 cells were infected with lentiviruses harboring a MYEOV overexpression vector [PANC-1 (MYEOV)] or its negative control blank vector [PANC-1 (NEG)] or with a MYEOV shRNA knockdown vector [PANC-1 (shMYEOV)] or its control negative blank vector [PANC-1 (shNEG)]. b, c Tumor volume (b) and tumor growth curves (c) after four types of stable cell lines were injected into NOD/SCID mice. All n ≥ 3; bar, SEM; *P < 0.05, **P < 0.01 and ***P < 0.001 compared with NC; Student’s t-test.