ABSTRACT
BACKGROUND:In recent years, based on high-throughput molecular imaging, integration of genomics, proteomics and computer aided design and the application of correlative “technical chains” have achieved great achievements in the research of breast cancer, lung cancer, gastric cancer, colon cancer, ovarian cancer and melanin tumor. However, there are few researches on oral squamous cel carcinoma. OBJECTIVE:To detect the gene expression profile of the oral squamous cel carcinoma tissue and normal paracarcinoma tissue using DNA chip-based gene expression profile. METHODS:Two samples of oral squamous cel carcinoma tissue and normal paracarcinoma tissue of patients who received treatment at Stomatological Hospital of Guangdong Province of China in 2013 were included in this study. The gene expression profiles of oral squamous cel carcinoma and normal paracarcinoma tissue were determined by the Roche NimbleGen gene expression microarrays. RESULTS AND CONCLUSION: According to screening criteria of differential genes, 7 872 out of 32 448 detected genes were differentialy expressed genes of oral squamous cel carcinoma, which accounts for 24% of the total number of the screening genes. 3 800 genes were up-regulated, and 4 072 were down-regulated. The results confirm that through detection with the help of gene expression profile clip, 7 872 differentialy expressed genes were obtained through DNA chip-based gene expression profiles according to the screening criteria. Thus it can be concluded that the occurrence and development of the tumors are not a result of single or several genes. Previous experiments based on a single or several genes have great limitations. These findings also suggest that the occurrence of tumor is a result of mutual regulatory effects of many genes forming a network, moreover, the interactions of the network is quite complicated.
ABSTRACT
<p><b>OBJECTIVE</b>To study the influence of ultraviolet (UV) irradiation on physical and chemical properties of sandblasted and acid-etched (SA) titanium surface and their ability to adsorb human fibronectin (HFn).</p><p><b>METHODS</b>SA and UV-SA surfaces were separately prepared. Surface morphology, roughness, elemental composition, wettability and HFn adsorption assay were performed for comparative analysis of these two surfaces.</p><p><b>RESULTS</b>SA and UV-SA surface had a similar morphology with multi-holes, and average roughness. UV-SA surface had a lower C content (22.83%) and higher O content (51.20%) and presented hydrophilicity, while SA surface showed hydrophobicity. But the quantity of adsorbed HFn on SA surface at 10 min assay point [(0.41 ± 0.07) µg] was statistically higher than that on UV-SA surface [(0.26 ± 0.08) µg](P = 0.007).</p><p><b>CONCLUSIONS</b>UV irradiation would not change the morphology and roughness of SA surface. However, it could reduce the hydrocarbon and increase the hydroxyl groups, and the absorption of HFn on UV-SA surface at 10 min assay point was statistically lower than that on SA surface. Therefore, the in-vitro bioactivity of UV-SA surface was not as good as that of SA surface.</p>