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Middle East Journal of Cancer، جلد ۱۳، شماره ۱، صفحات ۴۳-۵۵
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عنوان انگلیسی Safe Combination of Cisplatin and Metformin Reverts the Malignant Ascites in a Mouse Model to a Solid Tumor by Downregulation of ΔNp63 and Induces Tumor Dormancy via mTOR/ p21 Mechanism
چکیده انگلیسی مقاله Background: Currently, combination therapy has become the cornerstone of cancer treatment. The combination of different anticancer mechanisms can induce tumor cell quiescence. However, toxicity to normal tissue is the major limitation of existing combined drugs. Method: In this experimental study, Ehrlich ascites carcinoma (EAC) inoculated into mice was targeted with just one dose of cisplatin and later doses of metformin, a safe antidiabetic drug with an anticancer effect, to maintain EAC cells in the quiescent state and secure a longer survival time without tumor recurrence. Results: The group that underwent dual therapy developed a delayed solid tumor instead of a malignant ascites. The induction of chemo-quiescence in the EAC cells was proven by the downregulation of mechanistic target of rapamycin and the upregulation of cyclin-dependent kinase inhibitor 1 (p21) expressions. Intriguingly, the conversion of free neoplastic cells into a solid tumor was associated with a significant decrease in ΔNp63 immunostaining in EAC cells. Conclusion: Taken together, a single dose of cisplatin followed by metformin doses could overcome the aggressiveness of malignant ascites by the conversion into a solid tumor, induction of chemo-quiescence, and the extension of survival time.
کلیدواژه‌های انگلیسی مقاله Chemo-quiescence, Ehrlich ascites carcinoma, Mechanistic target of rapamycin (mTOR), Metformin, Cisplatin, ΔNp63
نویسندگان مقاله Sara Gebril |
Division of Biochemistry, Department of Chemistry, Faculty of Science, Mansoura University, Mansoura, Egypt

Om-Ali Elkhawaga |
Division of Biochemistry, Department of Chemistry, Faculty of Science, Mansoura University, Mansoura, Egypt

نشانی اینترنتی https://mejc.sums.ac.ir/article_47606_5f848f8303c6fb99ec199eeae5a45764.pdf
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