Aloe emodin, an anthraquinone of Aloe barbadensis Miller has been shown to have more cytotoxic effect in
different kinds of human cancer cell lines compared to normal. Accordingly, we found it to selectively inhibit
the proliferation of oestrogen-receptor-positive-(ER+)-breast cancer cells, MCF-7; but not controls cells,
MCF-10A. However, its precise mechanism is not well understood. Several studies have shown that there is
evidence of increased intracellular calcium (Ca2+), both at early and late stage of apoptosis which associated
with the down-regulation of ERK1/2 proliferative pathway. Therefore, we aim to elucidate the involvement
of intracellular Ca2+ in aloe emodin induced apoptosis on MCF-7. Apoptotic morphological changes were
observed under fluorescence microscope. The involvement of cytoplasmic Ca2+ and MAPKs were investigated
using Fluo-4 intracellular Ca2+ imaging and QuantiGene 2.0 Plex assay, respectively. IC50 of aloe emodin
(80 μM) at 72 hours incubation was used. Data were evaluated using the one-way or two-way ANOVA tests.
Our results indicated that aloe emodin at IC50 80µM induced apoptosis on MCF-7 through the association of
intracellular Ca2+ signalling. This observation include a significant increased (p