Liu et al (2008) screened for HCC cell lines (hepatocellular car

Liu et al. (2008) screened for HCC cell lines (hepatocellular carcinoma) with high expression levels of Rac1 (Ras-related C3 botulinum toxin substrate 1) to study the relationship between the inhibitory effect of melittin on HCC metastasis and the Rac1-mediated signaling pathway both in vitro and in vivo. They found that Rac1 plays a crucial role in the control of HCC cell motility and metastasis. Melittin prevents HCC metastasis via inhibition of Rac1. Melittin inhibited cell motility accompanied by a decrease in Rac1, ERK (extracellular signal-regulated kinase), and JNK (c-Jun N-terminal kinases) activity, suggesting that melittin acts through the suppression of Rac1-dependent pathways. In addition,

the lung metastasis rate was significantly

decreased in the melittin-treated nude mouse model LCID20. However, the authors showed that administration of high doses of melittin find more in vivo has its side effects, particularly liver injury and hemolysis. Considering that HCC usually develops in a background of chronic liver injury and impaired liver function, caution will be required in the clinical application of melittin. Finally, the authors commented that a mutation of Val 5 to Arg, Ala15 to Arg, and deletion of Leu15 in melittin significantly GDC-0068 in vivo reduces its adverse side effect of hemolysis, but retains its antibacterial effect ( Liu et al., 2008), showing that there are ways to overcome the toxic effects of melittin in the organism in order

to perform future clinical trials. Moon et al. (2008) elucidated the effect of melittin in human leukemic U937 cells and the underlying intracellular signal transduction pathways involved in regulating apoptosis. Melittin induced a dose-dependent inhibition of the proliferation in U937 cells. After 48 h of treatment with more than 2 mg/ml melittin, U937 cells exhibited morphological characteristics of apoptosis, including cell shrinkage and nuclear condensation. These results suggest that melittin-induced apoptosis contributes to the decreased proliferation of U937 cells. This apoptotic response was associated most with the upregulation of Bax and caspase-3 activation and downregulation of Bcl-2 and IAP (inhibitor of apoptosis) family members. Moreover, the inactivation of Akt displayed by cells treated with melittin also has an important role in the apoptosis process observed in these cells. In contrast, Tu et al. (2008) showed that melittin-induced apoptotic death in human melanoma A2058 cells was by a caspase-independent manner, through generation of ROS and subsequent disruption of mitochondrial membrane potential transition, followed by the release of AIF (Apoptosis Inducing Factor) and EndoG (Endonuclease G) into the nucleus. Besides that, the role of Ca2+ in cell death promoted by melittin was well established, once incubation of cells under calcium-free conditions effectively diminished BV-induced apoptosis.

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