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. 2018 Jul 13;9(54):30304–30323. doi: 10.18632/oncotarget.25717

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Copyright: © 2018 Gurushidhappa et al.

This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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(A-F) Detection of the PJLME induced apoptosis using Annexin-V assay. Cells were treated with PJLME (16.8μg/mL) and vehicle control (DMSO 0.1%) for 72h. (A) Vehicle treated MDA-MB-231cells, (B) PJLME treated MDA-MB-231 Cells, (C) Vehicle treated MCF-7 cells, (D) PJLME treated MCF-7 cells, (E) Vehicle treated HaCaT cells, and (F) PJLME treated HaCaT cells. (G). Bar diagram showing percentage of apoptotic population after the treatment of PJLME. ^*values that were significantly different (^*p < 0.05) from the control.