Small · 2008 · 95 citations · 44 references
MedicineOncologyPharmacologyCancer ImmunologyCancer PharmacologyTumor ImmunologyCytokines In Tumor ImmunityOncology PharmacologyTumor Microenvironment ModulationAnti-tumor Macrophage ResponsesAnticancer ActivityAnticancer Mechanism Of ActionCancer Cell Proliferation InhibitionHistological ResponseImmunomodulatory EffectsInnate Immunity PathwaysPeritoneal Macrophages
The tumor-inhibitory effect of C60(OH)x was tested on the murine H22 hepatocarcinoma model. Doses of 0.2 and 1.0 mg kg(-1) body weight both showed significant antitumor activity with tumor inhibition rates of 31.9 and 38.4%, respectively, when mice were treated for 17 consecutive days. The damnification of liver was prominently reduced. Furthermore, histological examination indicated that an envelope of fibroblasts and lymphocytes was formed surrounding tumor tissues in the C60(OH)x-treated group, which inhibited the infiltration of tumor to the neighboring normal skeleton muscle tissues. To understand the antitumor mechanism, the immunomodulatory activity of C60(OH)x was investigated. The results indicate that C60(OH)x enhances the phagocytosis of peritoneal macrophages and elevates the activity of arginase and acid phosphatase in vivo. The tumor necrosis factor alpha production of C60(OH)x-treated macrophages also increases in vitro. These results suggest that C60(OH)x can enhance the innate immunity of tumor-bearing mice, and therefore inhibits growth of the tumor.
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Nitric oxide as a secretory product of mammalian cells
Carl Nathan · The FASEB Journal · 1992 · 4.4K citations
Determination of arginase activity in macrophages: a micromethod
Inés Corraliza, María Luisa Campo, Germán Soler et al. · Journal of Immunological Methods · 1994 · 544 citations