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. 2020 Oct 28;10:18515. doi: 10.1038/s41598-020-75598-1

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© The Author(s) 2020

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 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/.

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Increase of autophagic markers in Sal-treated cells. (a) Samples from DMSO-treated control and Sal-treated (1.0 μM) cells immunoblotted for LC3B (*p < 0.05; **p < 0.01; n = 3). (b) Samples from DMSO-treated control and Sal-treated (1.0 μM) cells immunoblotted for Beclin-1 (n = 3). (c) SK-MEL-19-GFP-LC3B cells were treated with 1.0 μM Sal for the indicated period. (d) TEM images of SK-Mel-19 cells treated with or without 1.0 μM Sal for 24 h. Individual portraits of autophagosomes and lysosomes were represented in the subpanel along with the images showing autophagosome, lysosome fusion and autophagolysosome.