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. 2018 Mar 16;9(4):419. doi: 10.1038/s41419-018-0449-5

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© The Author(s) 2018

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. 4 — a, b IHC and IF analysis of autophagic protein expression in ovarian cancer samples. c,d Western blot analysis of autophagy proteins expressed in the no-chemotherapy group and chemosensitive group (***p < 0.001, **p < 0.01, *p < 0.05). e Immunofluorescence analysis of the no-chemotherapy group and chemosensitive group with LC3 (green) and LAMP2 (red) staining. Nuclei were counterstained with DAPI (blue). f qRT-PCR analysis of the average relative mRNA expression levels of autophagy-related genes in the no-chemotherapy group and chemosensitive group (**p < 0.01, *p < 0.05).