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Please use this identifier to cite or link to this item: http://dspace.unitywomenscollege.ac.in/xmlui/handle/123456789/1912
Title: Studies on the mode of action of synthetic diindolylmethane derivatives against triple negative breast cancer cells
Authors: Dr Jamsheena V
Keywords: anticancer drugs, apoptosis, breast cancer, signal transduction
Issue Date: Feb-2022
Publisher: Basic and linical pharmacology and toxicology
Abstract: Diindolylmethane (DIM) is a metabolic product of indole-3-carbinol (I3C), the major phytochemicals present in cruciferous vegetables, which can modulate multiple signalling pathways in cancer. The present study deals with the mechanism of action of two synthetic biaryl conjugates of DIM in triple nega￾tive breast cancer cells. Out of 12 DIM derivatives tested, two compounds, DIM-1 and DIM-4, exhibit cytotoxicity with GI50 values of 9.83 0.2195 μM and 8.726 0.5234 μM, respectively, in 2D culture. In 3D culture, DIM-1 and DIM-4 show GI50 values of 24.000 0.7240 μM and 19.230 0.3754 μM, respectively. The non-toxic nature of the compounds was also established by the toxicity studies using the zebrafish model system. The two compounds induced apoptosis and anoikis in the cancer cells, which was confirmed by morphological analysis, nuclear fragmentation, membrane integrity assay, cas￾pase activity measurements and modulation of pro/anti-apoptotic proteins. The compounds inhibited cell migration and MMP-2 and MMP-9 activities indicating their anti-metastatic property. They also reduced the expression of active Ras, phosphorylated forms of PI3K, Akt and mTOR. Immunofluores￾cence studies revealed the reduced expression of EGFR and pEGFR in treated cells. To conclude, DIM-1 and DIM-4 induced anti-breast cancer effects by blocking EGF receptor and subsequently inhibiting Ras-mediated PI3K-Akt– mTOR signalling pathway.
URI: http://dspace.unitywomenscollege.ac.in/xmlui/handle/123456789/1912
ISSN: 1742-7843
Appears in Collections:Journal Articles

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