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International Journal of Traditional Chinese Medicine ; (6): 666-668, 2017.
Article in Chinese | WPRIM | ID: wpr-620140

ABSTRACT

The study of vitiligo has made a huge progress due to the development of medical technology. Some new treatment idea, methods and integrated therapies have been considered as the trending alternatives. This paper summarized the treatment of different regular treatment combined with fire needling for vitiligo in clinic.

2.
Yonsei Medical Journal ; : 234-240, 2017.
Article in English | WPRIM | ID: wpr-126252

ABSTRACT

PURPOSE: MicroRNAs are small non-coding RNAs that play important roles in vascular smooth muscle cell (VSMC) function. This study investigated the role of miR-379 on proliferation, invasion, and migration of VSMCs and explored underlying mechanisms thereof. MATERIALS AND METHODS: MicroRNA, mRNA, and protein levels were determined by quantitative real-time PCR and western blot. The proliferative, invasive, and migratory abilities of VSMCs were measured by CCK-8, invasion, and wound healing assay, respectively. Luciferase reporter assay was used to confirm the target of miR-379. RESULTS: Platelet-derived growth factor-bb was found to promote cell proliferation and suppress miR-379 expression in VSMCs. Functional assays demonstrated that miR-379 inhibited cell proliferation, cell invasion, and migration. Flow cytometry results further showed that miR-379 induced apoptosis in VSMCs. TargetScan analysis and luciferase report assay confirmed that insulin-like growth factor-1 (IGF-1) 3'UTR is a direct target of miR-379, and mRNA and protein levels of miR-379 and IGF-1 were inversely correlated. Rescue experiments showed that enforced expression of IGF-1 sufficiently overcomes the inhibitory effect of miR-379 on cell proliferation, invasion, and migration in VSMCs. CONCLUSION: Our results suggest that miR-379 plays an important role in regulating VSMCs proliferation, invasion, and migration by targeting IGF-1.


Subject(s)
Humans , Apoptosis , Cell Movement/physiology , Cell Proliferation/physiology , Insulin , Insulin-Like Growth Factor I/physiology , MicroRNAs/physiology , Muscle, Smooth, Vascular/cytology , Proto-Oncogene Proteins c-sis/physiology , RNA, Messenger/metabolism , Real-Time Polymerase Chain Reaction , Sincalide/physiology , Wound Healing/physiology
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