Abstract

Melittin, a major component found in bee venom, is produced by the Apis species of the honey bee. In this study, the effect of melittin derived from Apis florea (Mel-AF), which is a wild honey bee species that is indigenous to Thailand, was investigated against human malignant melanoma (A375) cells. In this study, Mel-AF exhibited considerable potential in the anti-proliferative action of A375 cells. Subsequently, the cellular mechanism of Mel-AF that induced cell death was investigated in terms of apoptosis. As a result, gene and protein expression levels, which indicated the activation of cytochrome-c release and caspase-9 expression, eventually triggered the release of the caspase-3 executioner upon Mel-AF. We then determined that apoptosis-mediated cell death was carried out through the intrinsic mitochondrial pathway. Moreover, advanced abilities, including cell motility and invasion, were significantly suppressed. Mel-AF manipulated the actin arrangement via the trapping of stress fibers that were found underneath the membrane, which resulted in the defective actin cytoskeleton organization. Consequently, the expression of EGFR, a binding protein to F-actin, was also found to be suppressed. This outcome strongly supports the effects of Mel-AF in the inhibition of progressive malignant activity through the disruption of actin cytoskeleton-EGFR interaction and the EGFR signaling system. Thus, the findings of our current study indicate the potential usefulness of Mel-AF in cancer treatments as an apoptosis inducer and a potential actin-targeting agent.

Highlights

  • Malignant melanoma is the most serious form of skin cancer and originates from melanocyte.It has been associated with rapid progression and metastatic potential

  • We have demonstrated that synthetic melittin of A. florea (Mel-AF) and A. mellifera (Mel-AM) exhibited an anti-proliferative effect on human malignant melanoma (A375) cells in a dose-dependent manner

  • We have investigated the expression of the epidermal growth factor receptor (EGFR), a transmembrane tyrosine kinase that belongs to the ErbB family and which plays a crucial role in cell proliferation, differentiation and transformation

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Summary

Introduction

Malignant melanoma is the most serious form of skin cancer and originates from melanocyte.It has been associated with rapid progression and metastatic potential. The mortality rate of this disease has been increasing worldwide and conventional treatments such as surgery, chemoand radiation therapy are quite often unsuccessful [1,2] Besides these hindrances, this cancer is difficult to treat when the metastatic stage has developed. Various natural products and bioactive compounds have displayed effective activity in inhibiting the growth of many cancer cells on their own or in combination with other agents [4,5] They can induce cancer cell death via the apoptosis pathway [4], which is the ultimate goal of many chemotherapeutic agents and treatment strategies [6,7]. The development of a new effective bioactive agent that could stimulate the apoptotic cell death pathway would be extremely useful

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