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Icariin potentiates the antitumor activity of gemcitabine in gallbladder cancer by suppressing NF-κB

  
@article{APS6849,
	author = {Dian-cai Zhang and Jin-long Liu and Yong-bin Ding and Jian-guo Xia and Guo-yu Chen},
	title = {Icariin potentiates the antitumor activity of gemcitabine in gallbladder cancer by suppressing NF-κB},
	journal = {Acta Pharmacologica Sinica},
	volume = {34},
	number = {2},
	year = {2016},
	keywords = {},
	abstract = {Dian-cai ZHANG, Jin-long LIU, Yong-bin DING, Jian-guo XIA*, Guo-yu CHEN*
Department of General Surgery, The First Affiliated Hospital, Nanjing Medical University, Nanjing 210029, China

 
Aim: Gemcitabine has been increasingly prescribed for the treatment of gallbladder cancer.  However, the response rate is low.  The aim of this study is to determine whether icariin, a flavonoid isolated from Epimedi herba, could potentiate the antitumor activity of gemcitabine in gallbladder cancer.

Methods: Human gallbladder carcinoma cell lines GBC-SD and SGC-996 were tested.  Cell proliferation and apoptosis were analyzed using MTT assay and flow cytometry, respectively.  The expression of apoptosis- and proliferation-related molecules was detected with Western blotting.  Caspase-3 activity was analyzed using colorimetric assay, and NF-κB activity was measured with ELISA.  A gallbladder cancer xenograft model was established in female BALB/c (nu/nu) mice.  The mice were intraperitoneally administered gemcitabine (125 mg/kg) in combination with icariin (40 mg/kg) for 2 weeks.

Results: Icariin (40–160 µg/mL) dose-dependently suppressed cell proliferation and induced apoptosis in both GBC-SD and SGC-996 cells, with SGC-996 cells being less sensitive to the drug.  Icariin (40 µg/mL) significantly enhanced the antitumor activity of gemcitabine (0.5 µmol/L) in both GBC-SD and SGC-996 cells.  The mice bearing gallbladder cancer xenograft treated with gemcitabine in combination with icariin exhibited significantly smaller tumor size than the mice treated with either drug alone.  In GBC-SD cells, icariin significantly inhibited both the constitutive and gemcitabine-induced NF-κB activity, enhanced caspase-3 activity, induced G0-G1 phase arrest, and suppressed the expression of Bcl-2, Bcl-xL and surviving proteins.

Conclusion: Icariin, by suppressing NF-κB activity, exerts antitumor activity, and potentiates the antitumor activity of gemcitabine in gallbladder cancer.  Combined administration of gemcitabine and icariin may offer a better therapeutic option for the patients with gallbladder cancer.

 
Keywords: gallbladder cancer; GBC-SD cell; SGC-996 cell; cancer xenograft model; icariin; gemcitabine; NF-κB; cell cycle arrest; apoptosis; synergistic effect
 
This work was supported by grants from National Natural Science Foundation of China ( No 30901443) and from the Opening Project of Medical Key Disciplines in Jiangsu Province (No XK03 200904).
* To whom correspondence should be addressed. 
E-mail drjianguox@gmail.com (Jian-guo XIA); aroony@gmail.com (Guo-yu CHEN)
Received 2012-08-10    Accepted 2012-10-22},
	issn = {1745-7254},	url = {http://www.chinaphar.com/article/view/6849}
}