Articles you may be interested inSurface templates fabricated using a focused ion beam for lateral positioning of nanoscale islands on Si (001) substrates J. Vac. Sci. Technol. B 29, 04D106 (2011); 10.1116/1.3602112 Thickness effect on the dielectric, ferroelectric, and piezoelectric properties of ferroelectric lead zirconate titanate thin films Lead zirconic titanate ͑PZT͒ microscale island ͑1 m -100 nm͒ was fabricated by focused ion beam before its crystallization, followed by the annealing treatment at the crystallization temperature. Local electrical properties were evaluated by piezoresponse force microscopy technique. Compared to the PZT island fabricated after crystallization, the result shows that there is noticeable enhancement in nanoscale electrical properties of PZT island fabricated before crystallization, especially when the island size decreases. Raman spectra and Kelvin force microscopy result both show that there are little degradations on the PZT surface after this amorphous etching process. The mechanism will be discussed in this paper. These results are very beneficial to the development of the ferroelectric film applications in the dynamic random access memory, ferroelectric random access memory, and micro-electro-mechanical system field.
Cell migration-inducing hyaluronidase 1 (CEMIP), a Wnt-related protein and also known as KIAA1199, is implicated in the process of metastatic colonization in a variety of malignant tumors, including breast cancer (BC), which is one of the most frequently diagnosed tumors in women worldwide. In this study, multiple public databases, online analytical tools, and bioinformatics approaches were applied to explore the expression levels, regulatory mechanisms, and biological functions of CEMIP in BC. We illustrated that CEMIP was highly expressed in various kinds of carcinomas, including BC, especially advanced subtypes, and predicted less favorable prognosis (negatively associated with overall survival) in BC patients, which might be an independent prognostic factor. Then, we revealed that the mutation and high expression of CEMIP might lead to it as an oncogene. We also demonstrated that TP53 mutation, DNA hypo-methylation, and the expression changes of three potential upstream transcription factors (EZH2, EGR1, and JUN) of CEMIP were likely to cause the hyperexpression of CEMIP in BC. Moreover, our findings suggested that CEMIP might exert its carcinogenic roles in the tumor microenvironment via participation in the extracellular matrix formation, increasing cancer-associated fibroblast (CAF), M2 macrophage, and neutrophil infiltration and decreasing CD8+ T cell infiltration. In summary, our study provided more solid evidence for CEMIP as a prognostic and metastatic biomarker and a potential therapeutic target in BC. Of course, these findings also need more confirmations of basic experiments and further clinical trials in the future.
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