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J.Jpn. Surg. Soc.. 92(6): 734-739, 1991


Original article

EFFECTS OF SYNGENEIC PRESERVED BLOOD CELLS ON METASTATIC GROWTH OF THE LEWIS LUNG CARCINOMA

Department of Surgery I, National Defense Medical College, Tokorozawa, Japan
*) Naval Blood Research Laboratory, Boston University School of Medicine, Boston, U.S.A.

Takashi Ichikura, Shoetsu Tamakuma, Hideto Ito, Soichi Tomimatsu, C.Robert Valeri*)

Each of B6C3HF1 mice was infused with stored syngeneic blood cells, fresh syngeneic blood cells, or saline, and then was injected intravenously with 1×106 Lewis lung carcinoma cells. Survival rate of each group declined in order of the saline group, the fresh-cell group, and the stored-cell group with a significant difference between all paired groups (P<0.001). When the number of metastases and 125I-Iododeoxyuridine uptake in the lungs and livers were compared between these groups, there were significant differences with greater number and uptake in the stored-cell group than the fresh-cell group or the saline group on day 15 through 17, and greater in the fresh-cell group than the saline group on day 23 and 24. In the second experiment, each mouse was inoculated sptbcutaneously with 1×105 tumor cells. Twenty-one days later, the subcutaneous tumors were removed, and the mice were infused with blood cells or saline immediately. The number of lung metastases of the stored-cell group was significantly larger than that of the fresh-cell group or the saline group on 9 and 11 days following tumor removal. In conclusion, the transfusion of the preserved syngeneic blood cells was considered to enhance both artificial and spontaneous metastasis of the Lewis lung carcinoma.


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