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The different effects of recombinant human tumor necrosis factor on rat fibrosarcoma sublines
Authors:Junichi Ishihara  Nagahiro Saijo  Yasutsuna Sasaki  Hidehiko Nakano  Akira Ozaki  Hidenobu Takahashi  Masanori Sakurai  Kazuhiko Nakagawa  Masaaki Iigo  Fumihiko Kanzawa  Akio Hoshi  Weon Seon Hong  James R. Jett  Terumi Takahashi
Affiliation:(1) Pharmacology Division, National Cancer Center Research Institute, and Department of Internal Medicine, National Cancer Center Hospital, Tsukiji 5-1-1, Chuo-Ku, 104 Tokyo, Japan;(2) Department of Internal Medicine, Korea Cancer Center Hospital, 215-4, Gongneuny-dong, Dobong-ku, Seoul, Korea;(3) Department of Medicine, Mayo Medical School, 200 First Street, SW, 55906 Rochester, MN, USA;(4) Department of 1st Internal Medicine, Showa University, Hatanodai 1-5-8, Shinagawa-ku, 142 Tokyo, Japan
Abstract:Summary The antitumor effect of recombinant human tumor necrosis factor (rH-TNF) on two clones of rat fibrosarcoma with different metastatic potential to lymph nodes was examined. The colony formation of clone A, which has high metastatic potential, was completely inhibited by continuous exposure to rH-TNF at 50 U/ml. In contrast, colony formation of clone G, which has low metastatic potential, was not inhibited by high concentrations of rH-TNF (10,000 U/ml). The inhibitory effect of rH-TNF on colony formation by clone A was also observed with a 1-h exposure to rH-TNF. This effect was time and concentration dependent, as determined by the colony assay, 3H-thymidine uptake assay, and 51Cr-release assay. 3H-thymidine and 3H-uridine uptake per cell of clone A exposed to rH-TNF was not decreased. This suggests that the mechanisms of the antitumor effect of rH-TNF were not due to inhibition of DNA and RNA synthesis of tumor cells. In vivo growth and lymph node metastases of clone A inoculated i.p. to Donryu strain rats were completely suppressed by 14 consecutive i.p. injections of 105 or 106 U/kg per day of rH-TNF. On the other hand the growth of clone G was not influenced by rH-TNF administration.
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