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Cancer Immunology, Immunotherapy : CII logoLink to Cancer Immunology, Immunotherapy : CII
. 1991 Sep;33(5):346–349. doi: 10.1007/BF01756601

Treatment of chemically induced autochthonous rat mammary and colorectal carcinomas with interleukin-2

Martin R Berger 1,, Margaretha Salas 2, Felix Garzon 1, Edgar Petru 1, Udo Schwulera 3, Dietrich Schmähl 1
PMCID: PMC11038629  PMID: 1868493

Abstract

The antineoplastic efficacy of human interleukin-2 (IL-2) in autochthonous methylnitrosourea-induced mammary carcinoma and in acetoxymethly-methylnitrosamine-induced colorectal carcinoma of Sprague Dawley rats has been investigated. Under the conditions applied, IL-2 was non-toxic. In the mammary carcinoma IL-2 was therapeutically inactive. In the colorectal carcinoma, 1200 U IL-2/day exhibited significant antitumour activity in established tumours as well as in tumours treated “prophylactically” before their manifestation (P <0.05). The effect of IL-2 seemed to be more pronounced when given before manifestation of colorectal tumours (T/C = 8.7% vs 17.8% in established tumours). The differential sensitivity of the autochthonous mammary and colorectal carcinoma may be explained by differences in their proliferation rates and differences in volumes at the beginning of IL-2 therapy. IL-2 seems to be preferentially active in small tumours with a low proliferation rate, a feature typical of colon tumours

Key words: Rat mammary carcinomas, Colorectal carcinoma, Interleukin-2

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