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Comparative Activity of Chlonisol and Temozolomide in Mice After Intracranial Transplantation of Ehrlich Carcinoma and HER2-Positive Breast Cancer

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Pharmaceutical Chemistry Journal Aims and scope

In continuation of a preclinical study of the new alkylating anticancer drug chlonisol {2-[3-(2-chloroethyl)-3-nitrosoureido]-1,3-propanediol} created by us, its activity was assessed after intracranial transplantation of Ehrlich carcinoma and HER2-positive breast cancer into mice. Temozolomide, which is used in the treatment of malignant gliomas, was selected as an alkylating reference drug. Chlonisol significantly increased the median lifespan of tumor-bearing animals, surpassing temozolomide in activity for both tumor models. A comparison of survival curves of mice with HER2-positive breast cancer tumor transplants revealed no therapeutic effect of temozolomide, unlike an obvious increase in the survival of mice in the chlonisol group. Chlonisol can be a potential cytostatic agent in the chemotherapy of neoplastic lesions of the nervous system, which is extremely important in the treatment of HER2-positive breast cancer, which often metastasizes to the brain.

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Correspondence to V. A. Alexandrov.

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Translated from Khimiko-Farmatsevticheskii Zhurnal, Vol. 56, No. 9, pp. 24 – 27, September, 2022.

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Alexandrov, V.A., Stukov, A.N., Zmitrichenko, Y.G. et al. Comparative Activity of Chlonisol and Temozolomide in Mice After Intracranial Transplantation of Ehrlich Carcinoma and HER2-Positive Breast Cancer. Pharm Chem J 56, 1179–1182 (2022). https://doi.org/10.1007/s11094-022-02773-1

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  • DOI: https://doi.org/10.1007/s11094-022-02773-1

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