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Herbal melanin inhibits colorectal cancer cell proliferation by altering redox balance, inducing apoptosis, and modulating MAPK signaling.

Authors :
Al-Obeed O
El-Obeid AS
Matou-Nasri S
Vaali-Mohammed MA
AlHaidan Y
Elwatidy M
Al Dosary H
Alehaideb Z
Alkhayal K
Haseeb A
McKerrow J
Ahmad R
Abdulla MH
Source :
Cancer cell international [Cancer Cell Int] 2020 Apr 16; Vol. 20, pp. 126. Date of Electronic Publication: 2020 Apr 16 (Print Publication: 2020).
Publication Year :
2020

Abstract

Background: Colorectal carcinoma is one of the most deadly cancers that requests effective and safe chemotherapy. Evaluation of natural product-based anticancer drugs as adjuvant treatment with fewer side effects is largely unexplored research fields. Herbal melanin (HM) is an extract of the seed coats of Nigella sativa that modulates an inflammatory response through toll-like receptor 4 (TLR4). This TLR4 receptor is also involved in the modulation of apoptosis. We therefore explored the anticancer potential of HM and specifically its effect on the molecular mechanisms underlying adenocarcinoma and metastatic colorectal cancer (mCRC) cell death in vitro.<br />Methods: Cell viability was evaluated using the MTT assay. Cellular reactive oxygen species (ROS), glutathione levels, and apoptotic status were assessed using fluorometric and colorimetric detection methods. HM-induced apoptotic and other signaling pathways were investigated using Western blot technology and mitochondrial transition pore assay kit. TLR4 receptor downregulation and blockade were performed using siRNA technology and neutralizing antibody, respectively.<br />Results: Our results showed that HM inhibited the proliferation of the colorectal adenocarcinoma HT29 and mCRC SW620 cell lines. Furthermore, HM enhanced ROS production and decreased glutathione levels. HM-induced apoptosis was associated with mitochondrial outer membrane permeability and cytochrome c release, inhibition of the Bcl2 family proteins, and activation of caspase-3/-7. In addition, HM modulated MAPK pathways by activating the JNK pathway and by inhibiting ERK phosphorylation. TLR4 receptor downregulation enhanced HM-induced apoptosis while TLR4 receptor blockade partially alleviated HM-inhibited ERK phosphorylation.<br />Conclusion: Altogether, these findings indicate that HM exerts pro-apoptotic effects and inhibits MAPK pathway through TLR4 in mCRC and colorectal adenocarcinoma cells, suggesting HM as a promising natural-based drug for the treatment of colorectal cancer.<br />Competing Interests: Competing interestsThe authors declare no potential conflict of interest.<br /> (© The Author(s) 2020.)

Details

Language :
English
ISSN :
1475-2867
Volume :
20
Database :
MEDLINE
Journal :
Cancer cell international
Publication Type :
Academic Journal
Accession number :
32322173
Full Text :
https://doi.org/10.1186/s12935-020-01206-x