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British Journal of Cancer logoLink to British Journal of Cancer
. 1990 Dec;62(6):919–922. doi: 10.1038/bjc.1990.409

A chelating derivative of alpha-melanocyte stimulating hormone as a potential imaging agent for malignant melanoma.

D R Bard 1, C G Knight 1, D P Page-Thomas 1
PMCID: PMC1971552  PMID: 2257220

Abstract

A chelating derivative of alpha-melanocyte stimulating hormone (MSH) has been synthesised, in which two molecules of the hormone are cross-linked by diethylenetriamine pentaacetic acid (DTPA). This compound, bisMSH-DTPA, was equipotent with MSH in an in vitro tyrosinase assay with Cloudman S91 melanoma cells. When DBA/2 mice bearing the same tumour were injected with bisMSH-DTPA labelled with the gamma-emitting isotope indium-111 (111In), the radioactivity became rapidly associated with the melanoma tissue. By 24 h post-injection, radioactivity in tumour tissue was significantly higher (P less than 0.001) than in spleen, lung, brain, eye and skin. Uptake of radioactivity by the tumours was inhibited by a 200-fold molar excess of MSH, whereas uptake by liver, kidney, spleen, lung, brain, eye and skin was unaffected. We conclude that bisMSH-DTPA may offer an alternative to antibody targeting in the imaging of malignant melanoma.

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Selected References

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