Selective inhibition of liver cancer growth realized by the intrinsic toxicity of a quantum dot–lipid complex
Dan Shao,1,* Jing Li,1,* Fengying Guan,1 Yue Pan,1 Xuanang Xiao,1 Ming Zhang,1 Hong Zhang,2 Li Chen1,3 1Department of Pharmacology, College of Basic Medical Sciences, Jilin University, Changchun, People’s Republic of China; 2Van’t Hoff Institute for Molecular Sciences,...
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| Autores principales: | , , , , , , , |
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| Formato: | article |
| Lenguaje: | EN |
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Dove Medical Press
2014
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| Acceso en línea: | https://doaj.org/article/f78d0f4d01494ba2b949f14fa9080347 |
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| Sumario: | Dan Shao,1,* Jing Li,1,* Fengying Guan,1 Yue Pan,1 Xuanang Xiao,1 Ming Zhang,1 Hong Zhang,2 Li Chen1,3 1Department of Pharmacology, College of Basic Medical Sciences, Jilin University, Changchun, People’s Republic of China; 2Van’t Hoff Institute for Molecular Sciences, University of Amsterdam, Amsterdam, the Netherlands; 3School of Nursing, Jilin University, Changchun, People’s Republic of China *These authors contributed equally to this work Abstract: Using the intrinsic toxicity of nanomaterials for anticancer therapy is an emerging concept. In this work, we discovered that CdTe/CdS quantum dots, when coated with lipids (QD-LC) instead of popular liposomes, polymers, or dendrimers, demonstrated extraordinarily high specificity for cancer cells, which was due to the difference in the macropinocytosis uptake pathways of QD-LC between the cancer cells and the normal cells. QD-LC-induced HepG2 cell apoptosis was concomitant with the activation of the JNK/caspase-3 signaling pathway. Moreover, QD-LC treatment resulted in a delay in the latent period for microtumor formation of mouse hepatocarcinoma H22 cells and inhibited tumor growth, with a reduction of 53.2% in tumor volume without toxicity in major organs after intratumoral administrations to tumor-bearing mice. Our results demonstrate that QD-LC could be a very promising theranostic agent against liver cancer. Keywords: CdTe/CdS quantum dot–lipid complex, intrinsic nanotoxicity, selectivity, liver cancer therapy, macropinocytosis |
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