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Jingwu Bu,Xudong Chen,Liangpeng Hu,Hanqing Yang,Saisai Liu 한국콘크리트학회 2020 International Journal of Concrete Structures and M Vol.14 No.3
The quantificational exploration of the propagation law of fracture process zone (FPZ) is of great importance to the research on concrete fracture. This paper performed fracture experiments on pre-cracked concrete beams under various loading rates. Digital image correlation (DIC) method was applied to obtain the whole field displacement of concrete in the fracture test. The crack opening displacement (COD) and the evolution of FPZ were determined based on the whole field displacement. The results show that the length of FPZ first increases and then decreases with the development of the effective crack length and the maximum length of FPZ is about 60 mm. It can be found that the length of FPZ corresponding to the peak load decreases with the increase of loading rates. Based on the fictitious crack model, a bilinear softening model was established. According to the proposed model, the mechanical behavior and the propagation law of FPZ were analyzed. The bilinear softening model can reflect the microcrack development and the aggregate interlocking in the FPZ.
Inhibition of glutathione metabolism attenuates esophageal cancer progression
Liang Peng,Ruixia Linghu,Demeng Chen,Jing Yang,Xiaoxue Kou,Xiang-Zhen Wang,Yi Hu,Yi-Zhou Jiang,Junlan Yang 생화학분자생물학회 2017 Experimental and molecular medicine Vol.49 No.-
Esophageal squamous cell carcinoma (ESCC) is a deadly malignancy with regard to mortality and prognosis, and the 5-year survival rate for all patients diagnosed with ESCC remains poor. A better understanding of the biological mechanisms of ESCC tumorigenesis and progression is of great importance to improve treatment of this disease. In this study, we demonstrated that the glutathione metabolism pathway is highly enriched in ESCC cells compared with normal esophageal epithelial cells in an in vivo mouse model. In addition, treatment with L-buthionine-sulfoximine (BSO) to deplete glutathione decreased the ESCC tumor burden in mice, thus demonstrating the critical role of glutathione metabolism in ESCC progression. BSO treatment also led to decreased cell proliferation and activation of cell apoptosis in ESCC. Finally, BSO treatment blocked NF-kB pathway activation in ESCC. Our study reveals a new pathway that regulates ESCC progression and suggests that inhibition of glutathione metabolism may be a potential strategy for ESCC treatment