Abstract |
Interferon-gamma (IFN-gamma) can enhance the experimental metastatic ability of B16 melanoma. The in vitro treatment with IFN-gamma of four clones derived from the murine mammary adenocarcinoma TS/A increased the number of lung colonies observed after intravenous injection in syngeneic mice. The spontaneous metastatic ability of these clones was not altered by the IFN-gamma pretreatment nor by daily intratumor injection of low-dose IFN-gamma. The experimental metastatic ability in nude mice of the human rhabdomyosarcoma cell line RD was decreased by in vitro pretreatment with IFN-gamma. To study the role played by major histocompatibility complex gene products in the IFN-gamma-mediated enhancement of B16 experimental metastasis, a mutant B16 clone, B78H1, was transfected with the H-2Kb gene. B78H1 cells are not capable of expressing H-2b even after treatment with IFN-gamma; IFN-gamma readily induced high levels of H-2Kb in a set of transfected clones, but did not enhance their experimental metastatic ability.
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Authors | P L Lollini, C De Giovanni, G Nicoletti, K Scotlandi, L Landuzzi, P Nanni |
Journal | Tumori
(Tumori)
Vol. 75
Issue 4
Pg. 383-8
(Aug 31 1989)
ISSN: 0300-8916 [Print] United States |
PMID | 2510384
(Publication Type: Journal Article)
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Chemical References |
- H-2 Antigens
- Recombinant Proteins
- Interferon-gamma
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Topics |
- Animals
- H-2 Antigens
(genetics)
- Humans
- Interferon-gamma
(pharmacology)
- Mammary Neoplasms, Animal
(pathology)
- Mice
- Mice, Inbred BALB C
- Mice, Inbred C57BL
- Neoplasm Metastasis
- Recombinant Proteins
- Rhabdomyosarcoma
(pathology)
- Transfection
- Tumor Cells, Cultured
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