Abstract
Recombinant human inrerferon ɑA/D (IFNɑA/D) is known to be as active on murine cells as on human cells. We studied the antitumor effect of pure IFNɑA/D on Meth-A sarcoma subcutaneously transplanted into female syngeneic BALB/c mice. When administered systematically (intraperitoneally), IFNɑA/D was only marginally (but significantly, P<0.05) effective in inhibiting tumor growth. With intralesional injection, however, IFNɑA/D strongly suppressed the growth of Meth-A sarcoma, even leading to complete tumor regression and to subsequent immunity to Meth-A sarcoma cells in the host mice when the treatment was started early after tumor transplantation and with a high IFNɑA/D dose. We also found that treatment of mice with IFNɑA/D increased the level of serum ɑ1-acid glycoprotein, one of the acute-phase proteins.
Original language | English |
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Pages (from-to) | 413-418 |
Number of pages | 6 |
Journal | Japanese Journal of Cancer Research GANN |
Volume | 77 |
Issue number | 4 |
Publication status | Published - 1986 Jan 1 |
Keywords
- Antitumor effect
- Interferon
- Meth-A sarcoma— ɑ-Acid glycoprotein
ASJC Scopus subject areas
- Oncology
- Cancer Research