Abstract

BackgroundMelanoma is the most aggressive form of skin cancer, and the most rapidly expanding cancer in terms of worldwide incidence. Chemotherapeutic approaches to treat melanoma have been uniformly disappointing. A Brazilian complex homeopathic medication (CHM), used as an immune modulator, has been recommended for patients with depressed immune systems. Previous studies in mice have demonstrated that the CHM activates macrophages, induces an increase in the number of leukocytes and improves the murine response against Sarcoma-180.MethodsHere we studied the interaction of mouse lymph node lymphocytes, co-cultured in vitro with macrophages in the presence or absence of the CHM, with B16F10 melanoma cells.ResultsLymphocytes co-cultured with macrophages in the presence of the CHM had greater anti-melanoma activity, reducing melanoma cell density and increasing the number of lysed tumor cells. There was also a higher proportion of activated (CD25+) lymphocytes with increased viability. Overall, lymphocytes activated by treatment destroyed growing cancer cells more effectively than control lymphocytes.ConclusionCo-culture of macrophages with lymphocytes in the presence of the CHM enhanced the anti-cancer performance of lymphocytes against a very aggressive lineage of melanoma cells. These results suggest that non-toxic therapies using CHMs are a promising alternative approach to the treatment of melanomas. In addition, they are attractive combination-therapy candidates, which may enhance the efficacy of conventional medicines by improving the immune response against tumor cells.

Highlights

  • Melanoma is the most aggressive form of skin cancer, and the most rapidly expanding cancer in terms of worldwide incidence

  • Altered melanoma cell morphology An examination of cell cultures by light microscopy showed no morphological differences between B16F10 cells treated with the complex homeopathic medication (CHM) and untreated control cells (Fig 1A and 1B)

  • Lymphocytes previously in contact with macrophages and treated with the CHM were activated in some manner such that they were capable of destroying B16F10 melanoma cells, resulting in a lower density monolayer of

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Summary

Introduction

Melanoma is the most aggressive form of skin cancer, and the most rapidly expanding cancer in terms of worldwide incidence. Chemotherapeutic approaches to treat melanoma have been uniformly disappointing. Melanoma represents a significant worldwide public health risk, and from the standpoint of incidence, constitutes the fastest growing of all cancer types. Malign melanoma is the most aggressive form of skin cancer, with a mortality rate that has risen about 2% annually since 1960. There are few chemotherapeutic agents available for treating metastatic melanoma, and those that have been used have achieved uniformly disappointing results. No single chemotherapeutic agent currently offers a response rate greater than 25%, and treatment is invariably accompanied by significant side effects, including myelosuppression, nausea and emesis [1,2]

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