Browsing by Author "Wang, Hsiao-Wei"
Now showing 1 - 2 of 2
- Results Per Page
- Sort Options
Item type:Item, MicroRNA-30a inhibits cell migration and invasion by downregulating vimentin expression and is a potential prognostic marker in breast cancer(2012-08-01) ;Cheng, Chun-Wen ;Wang, Hsiao-Wei ;Chang, Chia-Wei ;Chu, Hou-WeiChen, Cheng-You"Tumor recurrence and metastasis result in an unfavorable prognosis for cancer patients. Recent studies have suggested that specific microRNAs (miRNAs) may play important roles in the development of cancer cells. However, prognostic markers and the outcome prediction of the miRNA signature in breast cancer patients have not been comprehensively assessed. The aim of this study was to identify miRNA biomarkers relating to clinicopathological features and outcome of breast cancer. A miRNA microarray analysis was performed on breast tumors of different lymph node metastasis status and with different progression signatures, indicated by overexpression of cyclin D1 and beta-catenin genes, to identify miRNAs showing a significant difference in expression. The functional interaction between the candidate miRNA, miR-30a, and the target gene, Vim, which codes for vimentin, a protein involved in epithelial-mesenchymal transition, was examined using the luciferase reporter assay, western blotting, and migration and invasion assays. The association between the decreased miR-30a levels and breast cancer progression was examined in a survival analysis. miR-30a negatively regulated vimentin expression by binding to the 3'-untranslated region of Vim. Overexpression of miR-30a suppressed the migration and invasiveness phenotypes of breast cancer cell lines. Moreover, reduced tumor expression of miR-30a in breast cancer patients was associated with an unfavorable outcome, including late tumor stage, lymph node metastasis, and worse progression (mortality and recurrence) (p < 0.05). In conclusion, these findings suggest a role for miR-30a in inhibiting breast tumor invasiveness and metastasis. The finding that miR-30a downmodulates vimentin expression might provide a therapeutic target for the treatment of breast cancer."Item type:Item, Mobile charging information management for smart grid networks(2013-04-01) ;Yang, Shun-Neng ;Wang, Hsiao-Wei ;Gan, Chai-Hien ;Lin, Yi-Bing資訊工程學系With today's electric charging technology, charging time of an electric vehicle (EV) is much longer than that for a gasoline vehicle, and therefore the queueing effect at an EV charging station (CS) may be serious. That is, when an EV arrives at an overloaded CS, it is likely that the EV will wait for a long time before it is charged. This paper investigates the waiting problem for EV charging. We propose a Mobile CS (MCS) management system to dynamically distribute charging pole support that reduces the waiting times of EVs incurred in a fixed CS. A Mobile Charging Information Management System (MC-IMS) is presented to describe the execution flow of the MCS service. Simulation experiments are conducted to investigate the waiting time performance for the proposed mechanism. Our study indicates that the MCS-based MC-IMS provides effective EV charging with short waiting times. (C) 2012 Elsevier Ltd. All rights reserved.