| Literature DB >> 27693706 |
Jun-Won Yun1, Jae Hun Ahn2, Euna Kwon1, Seung-Hyun Kim1, Hanna Kim1, Ja-June Jang3, Woo Ho Kim3, Ji Hyang Kim4, Su-Youne Han4, Jin Tac Kim4, Jong-Hoon Kim5, Wookhwan Kim6, Seung-Yup Ku7, Byung-Rok Do8, Byeong-Cheol Kang9.
Abstract
Umbilical cord-derived mesenchymal stem cells (UC-MSCs) therapy might be an alternative to liver transplantation for acute or chronic liver injury. The aim of this study was to evaluate the efficacy of human UC-MSCs on carbon tetrachloride (CCl4)-induced acute liver injury. In addition, its toxicity, tumorigenicity, and biodistribution were determined. Significant hepatoprotective effects of hUC-MSCs with decreased levels of hepatocellular necrosis and lobular neutrophilic infiltration were found. Regarding the safety of hUC-MSCs, no serious hUC-MSCs-related changes (body weight, food/water consumption, clinical symptom, urinalysis, hematology, clinical chemistry, organ weight, and histopathology) were observed in a 13-week subchronic toxicity study. In a 26-week tumorigenicity study, no mice developed tumor related to hUC-MSCs transplantation up to 1 × 108 cells/kg. In particular, human mitochondrial sequence detection revealed that most hUC-MSCs were cleared from the major organs of the mice at 13 weeks after transplantation. There was no systemic toxicity or neoplastic finding either. Taken together, these results suggested that hUC-MSCs have great potential for future clinical treatment of acute liver disease. Copyright ÂEntities:
Keywords: Biodistribution; Liver injury; Toxicity; Tumorigenicity; Umbilical cord-derived mesenchymal stem cells
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Year: 2016 PMID: 27693706 DOI: 10.1016/j.yrtph.2016.09.029
Source DB: PubMed Journal: Regul Toxicol Pharmacol ISSN: 0273-2300 Impact factor: 3.271