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Antioxidant-enzyme interaction in cancer Antioxidant-enzyme interactions are important in cancer progression and development

Mechanism of protection by S-(1,2-dicarboxyethyl)glutathione triester against acetaminophen-induced hepatotoxicity in rat hepatocytes

Kuehnelt et al., 2006

However, contrary to the tumor-promoting potential of many angiogenic agents, BPC-157 has been shown to inhibit uncontrolled cell proliferation, downregulate VEGF expression, and counteract VEGF-driven tumorigenesis, including suppression of Ki-67 and VEGF pathway activation [31, 73]

2,2-di-pyridylketone hydrazone dithiocarbamate s-butyric acid (DpdtbA) exhibits interesting antitumor activities against esophageal and gastric cancer