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Research ArticleExperimental Studies

Glycyrrhetinic Acid and Related Compounds Induce G1 Arrest and Apoptosis in Human Hepatocellular Carcinoma HepG2

YOSHIKO SATOMI, HOYOKU NISHINO and SHOJI SHIBATA
Anticancer Research November 2005, 25 (6B) 4043-4047;
YOSHIKO SATOMI
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  • For correspondence: ysatomi@koto.kpu-m.ac.jp
HOYOKU NISHINO
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SHOJI SHIBATA
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Abstract

Glycyrrhetinic acid (GA) and its related compounds are known to have anti-inflammatory activity and also to inhibit liver carcinogenesis and tumor growth. GA and related compounds inhibited cell proliferation of the human hepatoma cell line, HepG2. Among five compounds tested, ursolic acid and 18β-olean-12-ene-3β, 23, 28-triol (18β-erythrotriol) were comparatively effective, where the 50% inhibitory dose was 20 μM and 25 μM, respectively. Flow-cytometric analysis showed that GA and the related compounds arrested the cell cycle in the G1-phase; in addition, GA-related compounds induced apoptosis at high dose. Western blot analysis indicated that the induction of apoptosis by GA and ursolic acid was accompanied with an activation of caspase-8 and a reduction in the anti-apoptotic proteins, Bcl-2 and Bcl-xL, although the pro-apoptotic proteins, Bax and Bak, remained unaffected. These results suggest that GA and its related compounds may be potent agents in liver cancer treatment.

  • Glycyrrhetinic acid
  • glycyrrhizin
  • G1 arrest
  • apoptosis
  • Bcl-2 family
  • hepatocellular carcinoma

Footnotes

  • Received July 5, 2005.
  • Accepted August 30, 2005.
  • Copyright© 2005 International Institute of Anticancer Research (Dr. John G. Delinassios), All rights reserved
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Anticancer Research: 25 (6B)
Anticancer Research
Vol. 25, Issue 6B
1 Nov 2005
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Glycyrrhetinic Acid and Related Compounds Induce G1 Arrest and Apoptosis in Human Hepatocellular Carcinoma HepG2
YOSHIKO SATOMI, HOYOKU NISHINO, SHOJI SHIBATA
Anticancer Research Nov 2005, 25 (6B) 4043-4047;

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Glycyrrhetinic Acid and Related Compounds Induce G1 Arrest and Apoptosis in Human Hepatocellular Carcinoma HepG2
YOSHIKO SATOMI, HOYOKU NISHINO, SHOJI SHIBATA
Anticancer Research Nov 2005, 25 (6B) 4043-4047;
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