Re-evaluation of the anticarcinogenic effect of metformin in a chemically-induced hepatocellular carcinoma model not associated with diabetes

Fatima A. M. El-Deeb, Y. Mahmoud, N. H. Hassan
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Abstract

ABSTRACT Hepatocellular carcinoma (HCC) is the fourth cause of cancer mortality worldwide. Metformin is an antidiabetic drug that showed a prophylactic effect in the early stages of some cancers. This study aimed to reevaluate the anticarcinogenic effect of metformin in a cancer model not associated with diabetes. Also, to evaluate the effect of pharmacological antidiabetic dose of metformin (used in cancer studies) at the early stages of HCC versus the sub-pharmacological dose. HCC was induced by a single i.p injection of diethylnitrosamine followed by 16 biweekly i.p injections of carbon-tetrachloride. Metformin was i.p injected (25 or 250 mg/kg) post HCC induction for four weeks. The low dose of metformin suppressed HCC by reducing liver biomarkers levels, and the number and size of hepatic nodules. Also, metformin (25 mg/kg) downstaged HCC via activating Bax and suppressing Bcl-2, VEGF, and PCNA. Mice treated with metformin (250 mg/kg) exhibited lactic acidosis, death, and insignificant differences in nodules’ number and size and immunohistochemical markers compared to the HCC group. This study concluded that the pharmacological dose of metformin cannot be used at advanced stages of HCC, while the sub-pharmacological dose of metformin showed a promising anticarcinogenic effect in chemically-induced HCC model not associated with diabetes. .
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二甲双胍在与糖尿病无关的化学诱导肝细胞癌模型中的抗癌作用的再评价
肝细胞癌(HCC)是全球第四大癌症死亡原因。二甲双胍是一种抗糖尿病药物,在某些癌症的早期阶段显示出预防作用。本研究旨在重新评估二甲双胍在与糖尿病无关的癌症模型中的抗癌作用。此外,为了评估在HCC早期使用二甲双胍(用于癌症研究)的药理降糖剂量与亚药理剂量的效果。肝细胞癌的诱导方法是单次静脉注射二乙基亚硝胺,然后每两周静脉注射16次四氯化碳。肝细胞癌诱导后静脉注射二甲双胍(25或250 mg/kg) 4周。低剂量二甲双胍通过降低肝脏生物标志物水平和肝结节的数量和大小来抑制HCC。此外,二甲双胍(25mg /kg)通过激活Bax和抑制Bcl-2、VEGF和PCNA来降低HCC的分期。二甲双胍(250 mg/kg)治疗小鼠出现乳酸酸中毒、死亡,与HCC组相比,结节数量、大小和免疫组织化学标志物差异不显著。本研究认为,二甲双胍的药理剂量不能用于肝癌晚期,而亚药理剂量二甲双胍在与糖尿病无关的化学诱导肝癌模型中显示出良好的抗癌作用。
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