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Research Institute for Tuberculosis, Leprosy and Cancer, Sendai
Kobe University School of Medicine, Kobe, Japan
Correspondence: For reprints contact: Shumpei Takeda, Dept. of Radiology and Nuclear Medicine, Research Inst. of Tuberculosis, Leprosy and Cancer, Tohoku University, 4-12 Hirosemachi, Sendai 980, Japan.
ABSTRACT
Intracellular localization of Ga-67 and In-111 was investigated in Morris hepatoma 7316A and in normal Buffalo rat liver cells by a cell fractionation method at 48 hr after an intraperitoneal injection of the nuclides. Lysosomal fractions of the tumor and normal liver cells had the highest relative specific radioactivities of the nuclides (p < 0.001). In a gradual solubilization experiment, the release of the nuclides at the same time as the acid phosphatase from the lysosomal fractions (p < 0.001) was thought to indicate that lysosomes are the site of accumulation for both nuclides whether in tumor or normal liver cells. Fragility of the tumor lysosomes might be inferred from the significantly greater regression coefficient in relation to the lysosomal fraction of tumor cells than that of normal liver cells when labeled with Ga-67 (p < 0.001). The poorer confidence limit for the regression coefficient in relation to the lysosomal fraction of tumor cells labeled with Ga-67 seemed to indicate that Ga-67 determines lysosomal functions of tumor cells more precisely than In-111.
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