Xanthohumol inhibits STAT3 activation pathway leading to growth suppression and apoptosis induction in human cholangiocarcinoma cells

被引:31
|
作者
Dokduang, Hasaya [1 ,3 ]
Yongvanit, Puangrat [1 ,3 ]
Namwat, Nisana [1 ,3 ]
Pairojkul, Chawalit [2 ,3 ]
Sangkhamanon, Sakkarn [2 ,3 ]
Yageta, Mika Sakurai [4 ]
Murakami, Yoshinori [4 ]
Loilome, Watcharin [1 ,3 ]
机构
[1] Khon Kaen Univ, Fac Med, Dept Biochem, Khon Kaen 40002, Thailand
[2] Khon Kaen Univ, Fac Med, Dept Pathol, Khon Kaen 40002, Thailand
[3] Khon Kaen Univ, Fac Med, Liver Fluke & Cholangiocarcinoma Res Ctr, Khon Kaen 40002, Thailand
[4] Univ Tokyo, Inst Med Sci, Dept Canc Biol, Div Mol Pathol, Tokyo 1088639, Japan
基金
日本科学技术振兴机构;
关键词
cholangiocarcinoma; STAT3; xanthohumol; OPISTHORCHIS-VIVERRINI INFECTION; NF-KAPPA-B; CANCER CHEMOPREVENTION; ANGIOGENESIS; MACROPHAGES; PROTEINS; TARGETS; KINASE; FAMILY; SRC;
D O I
10.3892/or.2016.4584
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
STAT3 plays a significant role in the development of cholangiocarcinoma (CCA) associated with the liver fluke (Opisthorchis viverrini; Ov). Xanthohumol (XN), a prenylated flavonoid extracted from hops, has known anticancer activity and could potentially target STAT3. The present study determined the effect of XN on STAT3, as well as ascertained its usefulness against CCA. The CCA cell proliferation at 20 mu M and 50 mu M of XN was shown to inhibited, while 20 mu M partially inhibited IL-6-induced STAT3 activation. At 50 mu M, the inhibition was complete. The reduction in STAT3 activity at 20 and 50 mu M was associated with a significant reduction of CCA cell growth and apoptosis. We also found that the administration of 50 mu M XN orally in drinking water to nude mice inoculated with CCA led to a reduction in tumor growth in comparison with controls. In addition, apoptosis of cancer cells increased although there was no visible toxicity. The present study shows that XN can inhibit STAT3 activation both in vivo and in vitro due to suppression of the Akt-NF kappa B signaling pathway. XN should be considered as a possible therapeutic agent against CCA.
引用
收藏
页码:2065 / 2072
页数:8
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