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Japanese Journal of Cancer Research : Gann logoLink to Japanese Journal of Cancer Research : Gann
. 2002 Aug;93(8):874–882. doi: 10.1111/j.1349-7006.2002.tb01332.x

Induction of Apoptosis in Hepatocellular Carcinoma Cell Lines by Emodin

Xubin Jing 1,2, Noboru Ueki 1, Jidong Cheng 1,2, Hiroyasu Imanishi 1, Toshikazu Hada 1,✉
PMCID: PMC5927105  PMID: 12716464

Abstract

Previous experiments have shown that emodin is highly active in suppressing the proliferation of several tumor cell lines. However, it is not clear that emodin can induce growth inhibition of hepatoma cells. We have found that emodin induces apoptotic responses in the human hepatocellular carcinoma cell lines (HCC) Mahlavu, PLC/PRF/5 and HepG2. The addition of emodin to these three cell lines led to inhibition of growth in a time‐and dose‐dependent manner. Emodin generated reactive oxygen species (ROS) in these cells which brought about a reduction of the intracellular mitochondrial transmembrane potential (ΔΨm), followed by the activation of caspase–9 and caspase–3, leading to DNA fragmentation and apoptosis. Our findings demonstrate that ROS and the resulting oxidative stress play a pivotal role in apoptosis. Preincubation of hepatoma cell lines with the hydrogen peroxide‐scavenging enzyme, catalase (CAT) and cyclosporin A (CsA), partially inhibited apoptosis. These results demonstrate that enhancement of generation of ROS, ΔΨmdisruption and caspase activation may be involved in the apoptotic pathway induced by emodin.

Keywords: Emodin, Apoptosis, Reactive oxygen species, Mitochondrial transmembrane potential, Caspase

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