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Hydroxyanisole-induced regression of the Harding-Passey melanoma in mice

โœ Scribed by D. L. Dewey; F. W. Butcher; A. R. Galpine


Book ID
104504992
Publisher
John Wiley and Sons
Year
1977
Tongue
English
Weight
523 KB
Volume
122
Category
Article
ISSN
0022-3417

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โœฆ Synopsis


The drug p-hydroxyanisole (OHA) was found to inhibit the incorporation of 3H-thymidine in the Harding-Passey melanoma cells in culture. Because the cultured cells had lost some of their pigment-forming capacity, the enzyme tyrosinase was added to the culture. This greatly increased the sensitivity of the cells to OHA, strongly suggesting that cells producing the enzyme would be preferentially killed by the drug. An in-vivo study of the effect of OHA injected into tumour-bearing mice showed a beneficial effect, including increased survival time, reduction in tumour size and in many cases complete loss of tumour and no recurrence. An experiment with animals immunologically suppressed by radiation suggests that the effect is not an immunological one.


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The subcellular distribution of lysosoma
โœ R. Allan Mufson ๐Ÿ“‚ Article ๐Ÿ“… 1974 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 815 KB

## Abstract Differential centrifugation of homogenates of Hardingโ€Passey melanoma demonstrated that aryl sulfatase A and ฮฒโ€glucuronidase sediment with particles (i.e., lysosomes) distinct from those particles bearing tyrosinase (i.e., melanosomes). The sedimentation curves for the lysosomal enzymes