Three to 20 hr after an i.p. injection of 64Cu (half-life, 12.8 hr) into mice bearing Krebs ascites cells, a high amount of the radioisotope was recovered in the ascites cells themselves. In the control group, the radioisotope was mainly present in the liver. Similar amounts of 64Cu were recovered in regenerating as well as in normal liver, whereas in the liver of mice bearing ascites cells, this amount was lower by 40 to 50% regardless of the ascitic volume. Thus, the copper metabolism seems to be disturbed at the hepatic level in mice bearing ascites cells.

The distribution of 64Cu was analyzed in DNA, RNA, and proteins from cellular lysates fractionated by CsCI gradient. There was a uniform pattern of distribution in the macromolecules from ascites cells, while 64Cu was preferentially associated with the protein fraction from liver. Further experiments indicated that, in vivo, 64Cu was bound to the DNA of ascites cells.

1

This article is the first in a series of reports dealing with the possible use of the lethal effect of 64Cu decay in tumor control. This work was supported by the International Atomic Agency, Vienna, Austria (“Research Agreement Contract” 1918/R2/CF); by the financial support of the “Comité de Coordination” of the Institut Curie; by Institut National de la Santé et de la Recherche Médicale (Contract 78-4-042-3); and by the Ligue Nationale Française Contre le Cancer, Paris, France.

This content is only available via PDF.