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Original Research

Remarkable inhibitory effects of hybrid liposomes on growth of human colon cancer cells through induction of cell cycle arrest along with apoptosis

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Pages 1913-1920 | Published online: 08 Sep 2011
 

Abstract

Background

Hybrid liposomes can be prepared by simply sonicating a mixture of vesicular and micellar molecules in buffer solutions. In this study, we investigated the effects of hybrid liposomes on the growth of human colon cancer cells in vitro.

Methods

Hybrid liposomes (HL-n, n = 21, 23, 25) composed of L-α-dimyristoylphosphatidylcholine (DMPC) and polyoxyethylene(n) dodecyl ethers (C12(EO)n, n = 21, 23, 25) were prepared by the sonication method and their inhibitory effects on growth of human colon cancer HCT116 cells were examined in vitro.

Results

Significant growth inhibition of HCT116 cells was observed in the presence of HL-n. The fifty percent inhibitory concentration (IC50) of HL-n was less than half that of DMPC liposomes. Furthermore, fluorescence microscopic and flow cytometric analyses indicated that the markedly inhibitory effects of HL-n on the growth of HCT116 cells could be attained through the induction of cell cycle arrest at the G0/G1 phase along with apoptotic cell death.

Conclusion

It was found for the first time that HL-n can induce both cell cycle arrest and apoptosis in colon cancer cells. The findings in this study should contribute to novel chemotherapy for colon cancer.

Supplementary figure

Figure S1 Inhibitory effects of HL-n on the growth of HCT116 cells for 48 hours.

Abbreviation: DMPC, dimyristoylphosphatidylcholine.

Figure S1 Inhibitory effects of HL-n on the growth of HCT116 cells for 48 hours.Abbreviation: DMPC, dimyristoylphosphatidylcholine.

Acknowledgments

The technical assistance of Ms Yoko Tomita and Dr Mamiko Yukihara with this research was appreciated. This work was supported in part by a Grant-in-Aid for Science Research from the Ministry of Education, Science and Culture of Japan.

Disclosure

The authors have no conflicts of interest in this work.