PMID- 25647308 OWN - NLM STAT- MEDLINE DCOM- 20151201 LR - 20181202 IS - 1791-244X (Electronic) IS - 1107-3756 (Linking) VI - 35 IP - 4 DP - 2015 Apr TI - Transplantation of human umbilical cord-derived mesenchymal stems cells for the treatment of Becker muscular dystrophy in affected pedigree members. PG - 1051-7 LID - 10.3892/ijmm.2015.2084 [doi] AB - The regeneration of muscle tissue has been achieved using multipotent mesenchymal stem cells in mouse models of injured skeletal muscle. In the present study, the utility of multipotent human umbilical cord-derived mesenchymal stem cells (hUC-MSCs) in the treatment of Becker muscular dystrophy (BMD), a genetic disease where muscle tissue fails to regenerate, was examined in members from a pedigree affected by BMD. The disease status was evaluated in 4 affected pedigree members (II1, II2, II3 and III2; aged 50, 46, 42 and 6 years, respectively). The transplantation of the hUC‑MSCs (performed on 3 patients, I2, II3 and III2) was performed by infusion with an intravenous drip over a 30‑min period, and the patients were evaluated at 1, 3, 4 and 12 weeks following the procedure. The evaluation was based on physical characteristics, as well as on molecular testing for serum creatine kinase (CK) and lactate dehydrogenase (LDH) levels and a histological examination of muscle biopsies. The patients suffered no adverse reactions in response to the transplantation of the hUC‑MSCs. At 1 week following transplantation all 3 patients showed improvement in the muscle force of the limbs, muscle size and daily activity. The walking gait of patient III2 had improved by 1 week post-transplantation and reached a normal status by 12 weeks. Serum CK and LDH levels were decreased relative to the baseline levels. A histological examination of muscle biopsies displayed no obvious tissue regeneration. In conclusion, the treatment of patients with BMD using hUC-MSCs was safe and of therapeutic benefit that lasted for up to 12 weeks. hUC-MSCs are, therefore, a potential cell therapy-based treatment option for patients with muscular dystrophies. FAU - Li, Pang AU - Li P AD - Department of Hepatobiliary Surgery, Shandong Cancer Hospital, Jinan, Shandong 250011, P.R. China. FAU - Cui, Kai AU - Cui K AD - Department of Hepatobiliary Surgery, Shandong Cancer Hospital, Jinan, Shandong 250011, P.R. China. FAU - Zhang, Bo AU - Zhang B AD - Department of Hepatobiliary Surgery, Shandong Cancer Hospital, Jinan, Shandong 250011, P.R. China. FAU - Wang, Zhendan AU - Wang Z AD - Department of Hepatobiliary Surgery, Shandong Cancer Hospital, Jinan, Shandong 250011, P.R. China. FAU - Shen, Yangyang AU - Shen Y AD - Department of Hepatobiliary Surgery, Shandong Cancer Hospital, Jinan, Shandong 250011, P.R. China. FAU - Wang, Xiangyu AU - Wang X AD - Department of Hepatobiliary Surgery, Shandong Cancer Hospital, Jinan, Shandong 250011, P.R. China. FAU - Zhang, Jianbo AU - Zhang J AD - Department of Pathology, Shandong Cancer Hospital, Jinan, Shandong 250011, P.R. China. FAU - Tong, Feng AU - Tong F AD - The Dean's Office, Shandong Cancer Hospital, Jinan, Shandong 250011, P.R. China. FAU - Li, Sheng AU - Li S AD - Department of Hepatobiliary Surgery, Shandong Cancer Hospital, Jinan, Shandong 250011, P.R. China. LA - eng PT - Journal Article DEP - 20150130 PL - Greece TA - Int J Mol Med JT - International journal of molecular medicine JID - 9810955 RN - EC 1.1.1.27 (L-Lactate Dehydrogenase) RN - EC 2.7.3.2 (Creatine Kinase) SB - IM MH - Adolescent MH - Biopsy MH - Child MH - Creatine Kinase/blood MH - Humans MH - L-Lactate Dehydrogenase/blood MH - Male MH - *Mesenchymal Stem Cell Transplantation MH - Mesenchymal Stem Cells/*cytology MH - Muscle Strength MH - Muscle, Skeletal/metabolism/pathology MH - Muscular Dystrophy, Duchenne/blood/diagnosis/metabolism/*therapy MH - *Pedigree MH - Time Factors MH - Treatment Outcome MH - Umbilical Cord/*cytology EDAT- 2015/02/04 06:00 MHDA- 2015/12/15 06:00 CRDT- 2015/02/04 06:00 PHST- 2014/09/12 00:00 [received] PHST- 2015/01/20 00:00 [accepted] PHST- 2015/02/04 06:00 [entrez] PHST- 2015/02/04 06:00 [pubmed] PHST- 2015/12/15 06:00 [medline] AID - 10.3892/ijmm.2015.2084 [doi] PST - ppublish SO - Int J Mol Med. 2015 Apr;35(4):1051-7. doi: 10.3892/ijmm.2015.2084. Epub 2015 Jan 30.