Abstract |
The antineoplastic efficacy of human interleukin-2 (IL-2) in autochthonous methylnitrosourea-induced mammary carcinoma and in acetoxymethyl-methyl-nitrosamine-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 less than 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.
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Authors | M R Berger, M Salas, F Garzon, E Petru, U Schwulera, D Schmähl |
Journal | Cancer immunology, immunotherapy : CII
(Cancer Immunol Immunother)
Vol. 33
Issue 5
Pg. 346-9
( 1991)
ISSN: 0340-7004 [Print] Germany |
PMID | 1868493
(Publication Type: Journal Article)
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Chemical References |
- Antineoplastic Agents
- Carcinogens
- Interleukin-2
- methyl(acetoxymethyl)nitrosamine
- mafosfamide
- Methylnitrosourea
- Cyclophosphamide
- Dimethylnitrosamine
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Topics |
- Animals
- Antineoplastic Agents
(administration & dosage)
- Antineoplastic Combined Chemotherapy Protocols
(pharmacology)
- Carcinogens
- Colorectal Neoplasms
(chemically induced, drug therapy)
- Cyclophosphamide
(administration & dosage, analogs & derivatives)
- Dimethylnitrosamine
(analogs & derivatives)
- Female
- Interleukin-2
(administration & dosage, pharmacology)
- Male
- Mammary Neoplasms, Experimental
(chemically induced, drug therapy)
- Methylnitrosourea
- Neoplasm Transplantation
- Rats
- Rats, Inbred Strains
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