Metformin Induces Cell Cycle Arrest, Reduced Proliferation, Wound Healing Impairment In Vivo and Is Associated to Clinical Outcomes in Diabetic Foot Ulcer Patients

二甲双胍 医学 伤口愈合 哈卡特 细胞周期 细胞生长 药理学 流式细胞术 活力测定 安普克 内科学 糖尿病 细胞 内分泌学 癌症 外科 免疫学 生物 体外 细胞生物学 磷酸化 遗传学 蛋白激酶A 生物化学
作者
Fatima Ochoa-Gonzalez,Alberto R. Cervantes-Villagrana,Julio C. Fernández-Ruiz,Hilda S. Nava-Ramirez,Adriana C. Hernandez-Correa,José Antonio Enciso‐Moreno,Julio Enrique Castañeda‐Delgado
出处
期刊:PLOS ONE [Public Library of Science]
卷期号:11 (3): e0150900-e0150900 被引量:54
标识
DOI:10.1371/journal.pone.0150900
摘要

Background Several epidemiological studies in diabetic patients have demonstrated a protective effect of metformin to the development of several types of cancer. The underlying mechanisms of such phenomenon is related to the effect of metformin on cell proliferation among which, mTOR, AMPK and other targets have been identified. However, little is known about the role that metformin treatment have on other cell types such as keratinocytes and whether exposure to metformin of these cells might have serious repercussions in wound healing delay and in the development of complications in diabetic patients with foot ulcers or in their exacerbation. Material and Methods HaCaT Cells were exposed to various concentrations of metformin and cell viability was evaluated by a Resazurin assay; Proliferation was also evaluated with a colony formation assay and with CFSE dilution assay by flow cytometry. Cell cycle was also evaluated by flow cytometry by PI staining. An animal model of wound healing was used to evaluate the effect of metformin in wound closure. Also, an analysis of patients receiving metformin treatment was performed to determine the effect of metformin treatment on the outcome and wound area. Statistical analysis was performed on SPSS v. 18 and GraphPad software v.5. Results Metformin treatment significantly reduces cell proliferation; colony formation and alterations of the cell cycle are observed also in the metformin treated cells, particularly in the S phase. There is a significant increase in the area of the wound of the metformin treated animals at different time points (P<0.05). There is also a significant increase in the size and wound area of the patients with diabetic foot ulcers at the time of hospitalization. A protective effect of metformin was observed for amputation, probably associated with the anti inflammatory effects reported of metformin. Conclusions Metformin treatment reduces cell proliferation and reduces wound healing in an animal model and affects clinical outcomes in diabetic foot ulcer patients. Chronic use of this drug should be further investigated to provide evidence of their security in association with DFU.

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