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. 2020 Feb 17;53:9. doi: 10.1186/s40659-020-00275-6

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© The Author(s) 2020

Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.

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Fig. 2 — Overexpression of SNHG7 promoted cell proliferation as well as inhibited cell apoptosis and autophagy. a The expression of SNHG7 was detected in OA cells transfected with control, vector and lncRNA SNHG7 by qRT-PCR. b Cell proliferation was measured in OA cells (IL-1β) transfected with control, vector and lncRNA SNHG7 after transfection 24 h, 48 h, 72 h by MTT assay. c Cell apoptosis was detected in OA cells (IL-1β) transfected with control, vector and lncRNA SNHG7 by flow cytometry. d The protein expression of PCNA and cleaved-caspase 3 were measured in OA cells (IL-1β) transfected with control, vector and lncRNA SNHG7 by western blot. e The protein expression of beclin1 and LC3 were measured in OA cells (IL-1β) transfected with control, vector and lncRNA SNHG7 by western blot. *P < 0.05