Alkyl phosphocholines: Toxicity and anticancer properties
- 1 November 1987
- Vol. 22 (11) , 930-934
- https://doi.org/10.1007/bf02535558
Abstract
The study reports on the investigation of acute and subacute toxicity and on antineoplastic activity of hexadecylphosphocholine (HPC), the first compound of a new class of antineoplastic chemotherapeutics. In rats, the LD50 of HPC was 606 μmol/kg; the maximum tolerable dose over four weeks was 39 μmol/kg. Symptoms of toxicity were enteritis, spider cell activation in the liver, hemosiderosis in the spleen and reversible transaminase increase. The best therapeutic effect was observed on methylnitrosourea (MNU)‐induced mammary carcinoma in the rat. Two transplantable mammary carcinomas in the rat and autochthonous benzo(a)pyrene‐induced sarcomas exhibited low‐grade sensitivity to HPC. The MXT mammary carcinoma of the mouse, the Walker 256 carcinosarcoma of the rat, and autochthonous acetoxymethylmethylnitrosamine‐induced colonic tumors of the rat were not chemosensitive to HPC.Keywords
This publication has 8 references indexed in Scilit:
- Therapeutic activity of ET‐18‐OCH3 and hexadecylphosphocholine against mammary tumors in BD‐VI ratsLipids, 1987
- Noncarcinogenic chemotherapy with a combination of vincristine, methotrexate and 5-fluorouracil (VMF) in ratsInternational Journal of Cancer, 1983
- Chemotherapeutic studies on N-nitrosoacetoxymethyl-methylamine-and 1,2-dimethylhydrazine-induced colonic tumors in rats: Monotherapy with 5-fluorouracil, ftorafur, CGP 6809, and CGP 15'720AZeitschrift für Krebsforschung und Klinische Onkologie, 1982
- Preclinical drug development: rationale and methods.1981
- A Distribution-Free Test for Tumor-Growth Curve Analyses with Application to an Animal Tumor Immunotherapy ExperimentBiometrics, 1981
- Chemotherapy studies in autochthonous rat tumors intestinal cancerZeitschrift für Krebsforschung und Klinische Onkologie, 1978
- Einflu von Dosis und Tumorgr e f r das Ansprechen autochthoner Benzpyren-Sarkome bei Ratten und M usen auf chemotherapeutische Behandlung mit EndoxanZeitschrift für Krebsforschung und Klinische Onkologie, 1968