Dihydroartemisinin shift the immune response towards Th1, inhibit the tumor growth in vitro and in vivo.

Abstract

Some investigators have been found that Artemisinin and its derivates have inhibitory effect on growth of cancer cells. Among these derivatives, Dihydroartemisinin (DHA) is well known as a semi-synthetic one. In addition, T cells are proved to be essential for the destruction of cancer cells. In this research, we assessed the effects of DHA on tumor cell growth inhibition in vitro by MTT assay and in vivo by intra tumor injection of DHA against breast cancer. The results showed that the IC(50) values of DHA for RIN pancreatic tumor cell line were 30 μM and significant decrease in the tumor size in vivo. Also we evaluate the effect of DHA on the modulation of immune response in tumor bearing animals; these include the splenocyte proliferation using the BrdU kit; measurement of cytokine profile by ELISA, and evaluate the percentage of T regulatory cells in the spleen by flowcytometry. Our results demonstrated that a significant decrease in the level of IL-4 in the animals treated with DHA and significant decreased in the level of splenic CD4(+)CD25(+) Foxp3(+) T regulatory cells.

• Authors: Shokoofe Noori, Zuhair M Hassan
• Journal: Cellular immunology (Cell Immunol) Vol. 271 Issue 1 Pg. 67-72 ( 2011) ISSN: 1090-2163 [Electronic] Netherlands
• PMID: 21820106 (Publication Type: Journal Article)
• Copyright: Published by Elsevier Inc.

Chemical References

• Antimalarials
• Artemisinins
• Interleukin-4
• artenimol
• Interferon-gamma

Topics

• Animals
• Antimalarials (administration & dosage, pharmacology)
• Artemisinins (administration & dosage, pharmacology)
• Cell Line, Tumor
• Cell Proliferation (drug effects)
• Cell Survival (drug effects, immunology)
• Dose-Response Relationship, Drug
• Female
• Hindlimb (drug effects, immunology)
• Hypersensitivity, Delayed (immunology)
• Inhibitory Concentration 50
• Injections, Intraperitoneal
• Interferon-gamma (immunology, metabolism)
• Interleukin-4 (immunology, metabolism)
• Mammary Neoplasms, Experimental (immunology, pathology, prevention & control)
• Mice
• Mice, Inbred BALB C
• Sheep
• T-Lymphocytes (drug effects, immunology, metabolism)
• T-Lymphocytes, Regulatory (drug effects, immunology, metabolism)
• Th1 Cells (drug effects, immunology, metabolism)
• Tumor Burden (drug effects, immunology)