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Antitoxic and chemosensitizing effects of bovine lactoferrin and muramyl dipeptide in Ehrlich solid tumor-bearing mice treated with cisplatin

Authors :
Azza H. Mohamed
Dalia S Morsi
Amany E. Nofal
Gamalat Y. Osman
Hany M. Ibrahim
Mohamed L. Salem
Source :
International Journal of Cancer and Biomedical Research.
Publication Year :
2020
Publisher :
Egypts Presidential Specialized Council for Education and Scientific Research, 2020.

Abstract

Background: Despite the effectiveness of anti-cancer chemotherapy, it is associated with serious adverse side effects and the development of drug-resistance mechanisms. Immune dysfunction is considered one of the most serious adverse effects of anti-cancer chemotherapy, which increases the susceptibility of the patients to infection. Co-administration of immunomodulatory agents as adjuvant therapy with chemotherapy will result in better anti-tumor responses with fewer side effects. Aim: This study was designed to evaluate the ameliorative effects of bovine lactoferrin (bLF) and muramyl dipeptide (MDP) against toxicity induced by cisplatin in tumor-bearing mice. Materials and Methods: In this study, MDP or bLF was co-treated with cisplatin in mice bearing Ehrlich solid tumor (EST). Results: Co- treatment of cisplatin with MDP or bLF enhanced the anti-tumor effects of cisplatin to induce a reduction of the tumor size, proliferative capabilities of tumor cells accompanied by an elevation in the apoptotic profile of tumor cells. Moreover, co- treatments of Cisplatin with bLF or MDP reversed the Cisplatin-induced immune suppression and partially restored splenocyte proliferation, immune organ indices, hematological profile, liver and kidney functions, and histological structure. Conclusion: Both bLF and MDP were able to act as adjuvant therapy with anti-cancer chemotherapy through their abilities to enhance the chemotherapy curative effects, modulate the immune response against tumor cells, and to some extent ameliorate the adverse toxic effects of the chemotherapy.

Details

ISSN :
26822628
Database :
OpenAIRE
Journal :
International Journal of Cancer and Biomedical Research
Accession number :
edsair.doi...........77a2711bb776ab71eebeb1a46e161050
Full Text :
https://doi.org/10.21608/jcbr.2020.32770.1047