The Indolic Diet-Derivative, 3,3′-Diindolylmethane, Induced Apoptosis in Human Colon Cancer Cells through Upregulation of NDRG1
The Indolic Diet-Derivative, 3,3′-Diindolylmethane, Induced Apoptosis in Human Colon Cancer Cells through Upregulation of NDRG1
N-myc downstream regulated gene-1 participates in carcinogenesis, angiogenesis, metastases, and anticancer drug resistance. In the present study, we analyzed the expression pattern of N-myc downstream regulated gene-1 following treatment of human colonic cancer cell lines; HCT-116 (well differentiated with wild-type p53 gene) and Colo-320 (poorly differentiated with mutant p53 gene), with 3,3′-diindolylmethane, a well-established proapoptotic agent product derived from indole-3-carbinol. Treatment of Colo-320 and HCT-116 with 3,3′-diindolylmethane disclosed inhibition of cell viability in a dose-dependent manner, mediated through apoptosis induction. The increased expression of N-myc downstream regulated gene-1 was detected only in poorly differentiated colon cancer cells, Colo-320 cell line. Our results suggest that N-myc downstream regulated gene-1 expression is enhanced by 3,3′-diindolylmethane in poorly differentiated cells and followed by induction of apoptosis. 3,3′-diindolylmethane induced apoptosis may represent a new regulator of N-myc downstream regulated gene-1 in poorly differentiated colonic cancer cells.
- Technion – Israel Institute of Technology Israel
- University of Haifa Israel
- Technion Israel Institue of Technology Israel
- Carmel Medical Center Israel
Indoles, Cell Survival, Blotting, Western, Intracellular Signaling Peptides and Proteins, Apoptosis, Cell Cycle Proteins, Cell Differentiation, HCT116 Cells, Up-Regulation, Gene Expression Regulation, Neoplastic, Colonic Neoplasms, Anticarcinogenic Agents, Humans, Research Article
Indoles, Cell Survival, Blotting, Western, Intracellular Signaling Peptides and Proteins, Apoptosis, Cell Cycle Proteins, Cell Differentiation, HCT116 Cells, Up-Regulation, Gene Expression Regulation, Neoplastic, Colonic Neoplasms, Anticarcinogenic Agents, Humans, Research Article
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