Dokduang Hasaya, Yongvanit Puangrat, Namwat Nisana, Pairojkul Chawalit, Sangkhamanon Sakkarn, Yageta Mika Sakurai, Murakami Yoshinori, Loilome Watcharin
Department of Biochemistry, Faculty of Medicine, Khon Kaen University, Khon Kaen 40002, Thailand.
Department of Pathology, Faculty of Medicine, Khon Kaen University, Khon Kaen 40002, Thailand.
Oncol Rep. 2016 Apr;35(4):2065-72. doi: 10.3892/or.2016.4584. Epub 2016 Jan 21.
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 µM and 50 µM of XN was shown to inhibited, while 20 µM partially inhibited IL-6-induced STAT3 activation. At 50 µM, the inhibition was complete. The reduction in STAT3 activity at 20 and 50 µM was associated with a significant reduction of CCA cell growth and apoptosis. We also found that the administration of 50 µM 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-NFκB signaling pathway. XN should be considered as a possible therapeutic agent against CCA.
信号转导和转录激活因子3(STAT3)在与肝吸虫(华支睾吸虫;Ov)相关的胆管癌(CCA)发展中起重要作用。黄腐酚(XN)是一种从啤酒花中提取的异戊烯基黄酮,具有已知的抗癌活性,并且可能靶向STAT3。本研究确定了XN对STAT3的影响,并确定了其对CCA的有效性。结果显示,20μM和50μM的XN可抑制CCA细胞增殖,而20μM可部分抑制白细胞介素-6诱导的STAT3激活。在50μM时,抑制作用完全。20μM和50μM时STAT3活性的降低与CCA细胞生长和凋亡的显著减少有关。我们还发现,与对照组相比,给接种CCA的裸鼠经饮水口服50μM XN可导致肿瘤生长减少。此外,尽管没有明显毒性,但癌细胞的凋亡增加。本研究表明,XN可通过抑制Akt-NFκB信号通路在体内和体外抑制STAT3激活。XN应被视为一种可能的抗CCA治疗药物。