Issue 5, 2018

The dietary compound luteolin inhibits pancreatic cancer growth by targeting BCL-2

Abstract

Overexpression of the prosurvival protein BCL-2 contributes to malignant cell initiation, progression and resistance to treatment. Agents that function as its natural antagonists targeting BCL-2 must provide therapeutic benefit. In SW1990 pancreatic cancer cells, amplified BCL-2 was observed, which was believed to offer advantages for malignant cell survival and lead to poor patient outcome. Using structure-based virtual ligand screening, luteolin was found to be a natural small-molecule inhibitor of BCL-2, which exhibited dose–response proapoptosis activity in a BCL-2 dependent manner in vitro. The cellular thermal shift assay (CETSA) and notably competitive binding assay by the microscale thermophoresis (MST) method provided the evidence that this flavonoid directly bound to BCL-2. Mechanistic studies revealed that luteolin (compound 1) displaced BAX from the hydrophobic cleft of BCL-2, allowing mitochondrial permeabilization, and inducing SW1990 cancer cells to die. Meanwhile, luteolin represented significant tumor growth inhibition in an SW1990 xenograft model. Collectively, luteolin is rationally proved to trigger SW1990 cells to apoptosis by targeting BCL-2, and may serve as a potential agent for this cancer therapy.

Graphical abstract: The dietary compound luteolin inhibits pancreatic cancer growth by targeting BCL-2

Supplementary files

Article information

Article type
Paper
Submitted
05 Jan 2018
Accepted
13 Apr 2018
First published
19 Apr 2018

Food Funct., 2018,9, 3018-3027

The dietary compound luteolin inhibits pancreatic cancer growth by targeting BCL-2

Z. Li, Y. Zhang, L. Chen and H. Li, Food Funct., 2018, 9, 3018 DOI: 10.1039/C8FO00033F

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