Figure - PMC

Skip to main content

An official website of the United States government

Here's how you know

Here's how you know

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.

View full-text article in PMC

. 2022 Jul 19;15(14):5028. doi: 10.3390/ma15145028

Search in PMC
Search in PubMed
View in NLM Catalog
Add to search

© 2022 by the authors.

Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).

PMC Copyright notice

Inhibition of cellular proliferation and promotion of autophagy without induction of caspase-dependent apoptosis in B16F10 melanoma cell culture determined using Ann/PI (a), ApoStat (b), AO (c) and CFSE (e) staining, all performed after 48 h of treatment with SBA-15|XN3 and subsequently analyzed by flow cytometry. Dot plots and histograms are representative ones selected from three repeated experiments. The induction of autophagic cell death exposed to MC₅₀ dose SBA-15|XN3 and 3-MA (in final concentration of 1 mM) for 48 h (d). Cell viability was determined by CV assay and expressed as a percentage of control values (untreated cells). The data are presented as mean ± SD obtained from three independent experiments. * p < 0.05 refers to untreated cultures; # p < 0.05 refers to SBA-15|XN3 treated cultures.

Inhibition of cellular proliferation and promotion of autophagy without induction of caspase-dependent apoptosis in B16F10 melanoma cell culture determined using Ann/PI (a), ApoStat (b), AO (c) and CFSE (e) staining, all performed after 48 h of treatment with SBA-15|XN3 and subsequently analyzed by flow cytometry. Dot plots and histograms are representative ones selected from three repeated experiments. The induction of autophagic cell death exposed to MC₅₀ dose SBA-15|XN3 and 3-MA (in final concentration of 1 mM) for 48 h (d). Cell viability was determined by CV assay and expressed as a percentage of control values (untreated cells). The data are presented as mean ± SD obtained from three independent experiments. * p < 0.05 refers to untreated cultures; # p < 0.05 refers to SBA-15|XN3 treated cultures.