Junior Recital, Zhiqian Wu, piano

Junior RecitalZhiqian Wu, pianoFriday, March 29, 2019 at 7pmRecital Hall / James W. Black Music CenterThe presentation of this Junior Recital will fulfill in part the requirements for the Bachelor of Music degree in Performance. Zhiqian Wu studies piano with Dr. Sonia Vlahcevic and Dr. Yin Zheng

The impact of Metastasis Suppressor-1, MTSS1, on oesophageal squamous cell carcinoma and its clinical significance

<p>Abstract</p> <p>Background</p> <p>Metastasis suppressor-1 (MTSS1) has been proposed to function as a cytoskeletal protein with a role in cancer metastasis. Recent studies have demonstrated the clinical significance of MTSS1 in certain type of cancers, yet the clinical relevance of MTSS1 in oesophageal squamous cell carcinoma (ESCC) has not been reported.</p> <p>Methods</p> <p>In this study, we assessed the expression levels of MTSS1 in tumours and its matched adjacent non-tumour tissues obtained from 105 ESCC patients. We also used ESCC cells with differing MTSS1 expression and assessed the influence of MTSS1 on ESCC cells.</p> <p>Results</p> <p>Down-regulation of MTSS1 expression was observed both in oesophageal tumour tissues and ESCC cancer cell lines. We also reported that MTSS1 expression was associated with tumour grade (p = 0.024), lymph node metastasis (p = 0.010) and overall survival (p = 0.035). Patients with high levels of MTSS1 transcripts had a favorable prognosis in comparison with those who had reduced or absent expression levels. Using over-expression and knockdown approach, we created sublines from ESCC cells and further demonstrated that MTSS1 expression in ESCC cells significantly influenced the aggressiveness of the oesophageal cancer cells, by reducing their cellular migration and in vitro invasiveness.</p> <p>Conclusion</p> <p>MTSS1 serves as a potential prognostic indicator in human ESCC and may be an important target for cancer therapy.</p

Impact of diagenesis on the pore evolution and sealing capacity of carbonate cap rocks in the Tarim Basin, China

Analyzing the pore structure and sealing efficiency of carbonate cap rocks is essential to assess their ability to retain hydrocarbons in reservoirs and minimize leaking risks. In this contribution, the impact of diagenesis on the cap rocks' sealing capacity is studied in terms of their pore structure by analyzing rock samples from Ordovician carbonate reservoirs (Tarim Basin). Four lithology types are recognized: highly compacted, peloidal packstone-grainstone; highly cemented, intraclastic-oolitic-bioclastic grainstone; peloidal dolomitic limestone; and incipiently dolomitized, peloidal packstone-grainstone. The pore types of cap rocks include microfractures, intercrystalline pores, intergranular pores, and dissolution vugs. The pore structure of these cap rocks was heterogeneously modified by six diagenetic processes, including calcite cementation, dissolution, mechanical and chemical compaction, dolomitization, and calcitization (dedolomitization). Three situations affect the rocks' sealing capacity: (1) grainstone cap rocks present high sealing capacity in cases where compaction preceded cementation; (2) residual microfractures connecting adjacent pores result in low sealing capacity; and (3) increasing grain size in grainstones results in a larger proportion of intergranular pores being cemented. Four classes of cap rocks have been defined according to the lithology, pore structures, diagenetic alterations, and sealing performance. Class I cap rocks present the best sealing capacity because they underwent intense mechanical compaction, abundant chemical compaction, and calcite cementation, which contributed to the heterogeneous pore structures with poor pore connectivity. A four-stage, conceptual model of pore evolution of cap rocks is presented to reveal how the diagenetic evolution of cap rocks determines the heterogeneity of their sealing capacity in carbonate reservoirs.</p

Gene co-expression network analysis identifies BRCC3 as a key regulator in osteogenic differentiation of osteoblasts through a β-catenin signaling dependent pathway

Objective(s): The prognosis of osteoporosis is very poor, and it is very important to identify a biomarker for prevention of osteoporosis. In this study, we aimed to identify candidate markers in osteoporosis and to investigate the role of candidate markers in osteogenic differentiation. Materials and Methods: Using Weighted Gene Co-Expression Network analysis, we identified three hub genes might associate with osteoporosis. The mRNA expression of hub genes in osteoblasts from osteoporosis patients or healthy donor was detected by qRT-PCR. Using siRNA and overexpression, we investigated the role of hub gene BRCC3 in osteogenic differentiation by alkaline phosphatase staining and Alizarin red staining. Moreover, the role of β-catenin signaling in the osteogenic differentiation was detected by using β-catenin signaling inhibitor XAV939.Results: We identified three hub genes that might associate with osteoporosis including BRCC3, UBE2N, and UBE2K. UBE2N mRNA and UBE2K mRNA were not changed in osteoblasts isolated from osteoporosis patients, compared with healthy donors, whereas BRCC3 mRNA was significantly increased. Depletion of BRCC3 promoted the activation of alkaline phosphatase and formation of calcified nodules in osteoblasts isolated from osteoporosis patients and up-regulated β-catenin expression. XAV939 reversed the BRCC3 siRNA-induced osteogenic differentiation. Additionally, inhibited osteogenic differentiation was also observed after BACC3 overexpression, and this was accompanied by decreased β-catenin expression.Conclusion: BRCC3 is an important regulator for osteogenic differentiation of osteoblasts through β-catenin signaling, and it might be a promising target for osteoporosis treatment