Abstract

In order to develop melanoma-targeted in situ peptide vaccine immunotherapy, magnetite nanoparticles were conjugated with a melanogenesis substrate, N-propionyl cysteaminylphenol (NPrCAP). Magnetite nanoparticles introduced thermotherapy which caused non-apoptotic cell death and generation of heat shock protein (HSP) upon exposure to alternating magnetic field (AMF). NPrCAP was expected to develop a melanoma-targeted therapeutic drug because of its selective incorporation into melanoma cells and production of highly reactive free radicals, that result in not only oxidative stress but also apoptotic cell death by reacting with tyrosinase.

Highlights

  • Management of metastatic melanoma is extremely difficult challenge for physicians and scientists

  • In order to develop melanoma-targeted in situ peptide vaccine immunotherapy, magnetite nanoparticles were conjugated with a melanogenesis substrate, N-propionyl cysteaminylphenol (NPrCAP)

  • We provide evidence that melanoma-targeted in situ peptide vaccine immunotherapy has been successfully developed by conjugation of magnetite nanoparticles with a chemically modified melanogenesis substrate, and that a novel melanomatargeted chemo-thermo-immunotherapy (CTI Therapy) is provided for patients suffering from advanced metastatic

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Summary

Introduction

Management of metastatic melanoma is extremely difficult challenge for physicians and scientists. N-propionyl and N-acetyl derivatives of 4S-cysteaminylphenol (NPrand NAcCAP) were synthesized, and found to possess cytotoxic effects on in vivo and in vitro melanomas through the oxidative stress that derives from production of cytotoxic free radicals [17,18,19,20,21]. Based upon these rationales, we provide evidence that melanoma-targeted in situ peptide vaccine immunotherapy has been successfully developed by conjugation of magnetite nanoparticles with a chemically modified melanogenesis substrate, and that a novel melanomatargeted chemo-thermo-immunotherapy (CTI Therapy) is provided for patients suffering from advanced metastatic. Conjugation of Magnetite Nanoparticles with Melanogenesis Substrate, NPrCAP Provides Melanoma Targeted, in Situ Peptide Vaccine Immunotherapy through HSP Production by Chemo-Thermotherapy melanoma

Melanogenesis Cascade in Melanoma Cells
In Vivo Chemo-Thermo-Immunotherapy in
Production of Heat Shock Protein by Chemothermo-Immunotherapy Using
Melanocytotoxic and Immunogenic
Discussion
Summary and Conclusion
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