RETRACTED: Frondoside A Suppressive Effects on Lung Cancer Survival, Tumor Growth, Angiogenesis, Invasion, and Metastasis (Retracted Article)

被引:51
作者
Attoub, Samir [1 ]
Arafat, Kholoud [1 ]
Gelaude, An [2 ]
Al Sultan, Mahmood Ahmed [1 ]
Bracke, Marc [2 ]
Collin, Peter [3 ]
Takahashi, Takashi [4 ]
Adrian, Thomas E. [5 ]
De Wever, Olivier [2 ]
机构
[1] UAE Univ, Fac Med & Hlth Sci, Dept Pharmacol & Therapeut, Al Ain, U Arab Emirates
[2] Univ Hosp, Lab Expt Canc Res, Ghent, Belgium
[3] Coastside Bio Resources, Stonington, ME USA
[4] Nagoya Univ, Grad Sch Med, Div Mol Carcinogenesis, Ctr Neurol Dis & Canc, Nagoya, Aichi 4648601, Japan
[5] UAE Univ, Fac Med & Hlth Sci, Dept Physiol, Al Ain, U Arab Emirates
来源
PLOS ONE | 2013年 / 8卷 / 01期
关键词
CUCUMARIA-FRONDOSA; SEA-CUCUMBER; TRITERPENE GLYCOSIDE; PANCREATIC-CANCER; NATURAL-PRODUCTS; DRUG DEVELOPMENT; EXTRACT;
D O I
10.1371/journal.pone.0053087
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
A major challenge for oncologists and pharmacologists is to develop less toxic drugs that will improve the survival of lung cancer patients. Frondoside A is a triterpenoid glycoside isolated from the sea cucumber, Cucumaria frondosa and was shown to be a highly safe compound. We investigated the impact of Frondoside A on survival, migration and invasion in vitro, and on tumor growth, metastasis and angiogenesis in vivo alone and in combination with cisplatin. Frondoside A caused concentration-dependent reduction in viability of LNM35, A549, NCI-H460-Luc2, MDA-MB-435, MCF-7, and HepG2 over 24 hours through a caspase 3/7-dependent cell death pathway. The IC50 concentrations (producing half-maximal inhibition) at 24 h were between 1.7 and 2.5 mu M of Frondoside A. In addition, Frondoside A induced a time- and concentration-dependent inhibition of cell migration, invasion and angiogenesis in vitro. Frondoside A (0.01 and 1 mg/kg/day i.p. for 25 days) significantly decreased the growth, the angiogenesis and lymph node metastasis of LNM35 tumor xenografts in athymic mice, without obvious toxic side-effects. Frondoside A (0.1-0.5 mu M) also significantly prevented basal and bFGF induced angiogenesis in the CAM angiogenesis assay. Moreover, Frondoside A enhanced the inhibition of lung tumor growth induced by the chemotherapeutic agent cisplatin. These findings identify Frondoside A as a promising novel therapeutic agent for lung cancer.
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页数:10
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