1.The Therapeutic Potential of Stem Cells and Progenitor Cells for the Treatment of Parkinson's Disease.
Mooi Tiong LIAU ; Farahnaz AMINI ; Thamil Selvee RAMASAMY
Tissue Engineering and Regenerative Medicine 2016;13(5):455-464
Parkinson's disease (PD) is the second most common neurodegenerative disorder. It is usually seen in those above 50 years old. Current medical treatments only provide symptomatic relief but cannot cure the disease. There are claims that PD can be cured by stem cell transplant. The present study is aimed to assess the clinical potency and safety of stem cell in treating PD. A total of eleven articles were included for analysis, with four randomised control trials (RCTs), five non-RCTs and 2 follow up studies. All the four non-RCTs showed improvement of Unified Parkinson's Disease Rating Scale with no adverse events. However, results from RCTs showed no significant differences in the rating score among the transplant group and the Sham surgery group. The secondary analysis of one study showed a significant improvement of the rating score in those patients aged 60 and younger. Transplant group also associated with an overall higher incidence of adverse events. In conclusion, the RCTs and non-RCTs produced opposite results. When the studies were performed as non-RCTs in small number of patients, they showed promising result in the patients. It could say that currently the use of stem cell/progenitor cells in treating PD need much research despite having the implanted stem cell to be able to survive and integrated. The survival of implanted dopamine neurons in the striatum, however, does not indicate a success in correcting PD symptoms. Further investigations will shed light on the application and mechanism of action of stem cells in treating PD.
Cell- and Tissue-Based Therapy
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Dopaminergic Neurons
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Follow-Up Studies
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Humans
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Incidence
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Neurodegenerative Diseases
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Parkinson Disease*
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Stem Cell Transplantation
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Stem Cells*
2.Phytoestrogen (Daidzein) Promotes Chondrogenic Phenotype of Human Chondrocytes in 2D and 3D Culture Systems.
Suhaeb A MAHMOD ; Simmrat SNIGH ; Ivan DJORDJEVIC ; Yong Mei YEE ; Rohana YUSOF ; Thamil Selvee RAMASAMY ; Hussin A ROTHAN
Tissue Engineering and Regenerative Medicine 2017;14(2):103-112
Clinical investigations have shown a significant relationship between osteoarthritis (OA) and estrogens levels in menopausalwomen. Therefore, treatment with exogenous estrogens has been shownto decrease the risk ofOA.However, the effect estrogen has not been clearly demonstrated in the chondrocytes using phytoestrogens, which lack the specific side-effects of estrogens, may provide an alternative therapy. This study was designed to examine the possible effects of phytoestrogen (daidzein) on human chondrocyte phenotype and extracellular matrix formation. Phytoestrogens which lack the specific side-effects of estrogens may provide beneficial effect without causing hormone based side effect. Human chondrocytes cells were cultured in 2D (flask) and 3D (PCL-CA scaffold) systems. Daidzein cytotoxic effect was determined by MTT assay. Chondrocyte cellular content of glycosaminoglycans (GAGs), total collagen and chondrogenic gene expression were determined in both culture systems after treatment with daidzein.Daidzein showedtime-dependent and dose-independent effects on chondrocyte bioactivity.Thecompound at low doses showed significant (p<0.05) increase in total collagen andGAGsproduction at similar levels in 2Dand 3Dculture environment. The mRNA levels of Collagen II and Sox9 were increased significantly (p<0.01) after the treatment while the upregulation in COMP expression was statistically insignificant (p>0.05). The expression levels of Fibronectin, Laminin and Integrin b1were significantly increased especially in3Dculture system. This studywas illustrated the potential positive effects of daidzein onmaintenance of human chondrocyte phenotype and extracellular matrix formation suggesting an attractive and viable alternative therapy for OA.
Chondrocytes*
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Collagen
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Estrogens
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Extracellular Matrix
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Fibronectins
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Gene Expression
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Glycosaminoglycans
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Humans*
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Laminin
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Osteoarthritis
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Phenotype*
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Phytoestrogens*
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RNA, Messenger
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Up-Regulation