BMI-1 Autoantibody as a New Potential Biomarker for Cervical Carcinoma

BMI-1 is overexpressed in a variety of cancers, which can elicit an immune response leading to the induction of autoantibodies. However, BMI-1 autoantibody as a biomarker has seldom been studied with the exception of nasopharyngeal carcinoma. Whether BMI-1 autoantibodies can be used as a biomarker for cervical carcinoma is unclear. In this study,BMI-1 proteins were isolated by screening of a T7 phage cDNA library from mixed cervical carcinoma tissues. We analyzed BMI-1 autoantibody levels in serum samples from 67 patients with cervical carcinoma and 65 controls using ELISA and immunoblot. BMI-1 mRNA or protein levels were over-expressed in cervical carcinoma cell lines. Immunoblot results exhibited increased BMI-1 autoantibody levels in patient sera compared to normal sera. Additionally, the results for antibody affinity assay showed that there was no difference between cervical polyps and normal sera of BMI-1 autoantibody levels, but it was significantly greater in patient sera than that in normal controls (patient 0.827±0.043 and normal 0.445±0.023; P<0.001). What's more, the levels of BMI-1 autoantibody increased significantly at stage I (0.672±0.019) compared to normal sera (P<0.001), and levels of BMI-1 autoantibodies were increased gradually during the tumor progression (stage I 0.672±0.019; stage II 0.775 ±0.019; stage III 0.890 ±0.027; stage IV 1.043±0.041), which were significantly correlated with disease progression of cervical carcer (P<0.001). Statistical analyses using logistic regression and receiver operating characteristics (ROC) curves indicated that the BMI-1 autoantibody level can be used as a biomarker for cervical carcinoma (sensitivity 0.78 and specificity 0.76; AUC = 0.922). In conclusion, measuring BMI-1 autoantibody levels of patients with cervical cancer could have clinical prognostic value as well as a non-tissue specific biomarker for neoplasms expressing BMI-1

Loading Rate Effect on Nanohardness of Soda-Lime-Silica Glass

To understand how hardness, the key design parameter for applications of brittle solids such as glass concerning contact deformation, is affected by loading rate variation, nanoindentation with a Berkovich tip was used to measure the nanohardness of a 330-mu m-thick soda-lime-silica glass as a function of loading rate (1 to 1000 mN center dot s(-1)). The results showed for the very first time that, with variations in the loading rate, there was a 6 to 9 pct increase in the nanohardness of glass up to a threshold loading rate (TLR), whereafter it did not appreciably increase with further increase in loading rate. Further, the nanohardness data showed an indentation size effect (ISE) that obeyed the Meyer's law. These observations were explained in terms of a strong shear stress component developed just beneath the nanoindenter and the related shear-induced deformation processes at local microstructural scale weak links. The significant or insignificant presence of shear-induced serrations in load depth plots and corresponding scanning electron microscopic evidence of a strong or mild presence of shear deformation bands in and around the nanoindentation cavity supported such a rationalization. Finally, a qualitative picture was developed for different deformation processes induced at various loading rates in glass