Oral squamous cell carcinoma (OSCC) is the most common type of oral malignancy. Numerous therapies have been proposed for its cure. Research is continually being conducted to develop new forms of treatment as current therapies are associated with numerous side-effects. Luteolin, a common dietary flavonoid, has been demonstrated to possess strong anti-cancer activity against various human cancer cell lines. Nevertheless, research into luteolin-based anticancer activity against oral cancer remains scarce. Thus, the objective of this study was to assess the effect of luteolin as an anti-cancer agent. After treatment with luteolin, Ca9-22 and CAL-27 oral cancer cells showed condensed nuclei and enhanced apoptotic rate with evidence of mitochondria-mediated apoptosis. Epithelial-mesenchymal transition (EMT) is closely related to tumor migration and invasion. Luteolin suppressed cancer cell invasion and migration in the current study. Elevated expression of E-cadherin, an adherens junction protein, was evident in both cell lines after luteolin treatment. Luteolin also significantly inhibited transcription factors (i.e., N-cadherin, Slug, Snail, Twist, and ZEB-1) that regulated expression of tumor suppressors such as E-cadherin based on Western blot analysis and quantitative PCR. Thus, luteolin could induce mitochondrial apoptosis and inhibit cancer cell invasion and migration by suppressing EMT-induced transcription factors.

White-backed planthopper, Sogatella furcifera (Horváth) (Hemiptera: Delphacidae), is known as a long-range migratory pest in Asia. Although exact primary source of S. furcifera in Korea remains unknown. We used twelve microsatellite markers (SSR) to analyze the population genetic structure of the pest. We collected S. furcifera from Asia in 2012 (Korea, Laos, Nepal, Thailand, Vietnam and four different sites of Bangladesh), 2013 (China, Nepal, Thailand, two different sites of Bangladesh, and fifteen different sites of Korea), and 2014 (four different sites of China and ten different sites of Korea). To verify the genetic variance, we used STRUCTURE program to obtain structure analysis of K and K showed in three components in genetic clustering. Result in sample 2012, similar genetic structure showed in Korea and Vietnam. In 2013 and 2014, various genetic structure revealed in different sites of Korea and Asian population genetic structure appeared as on large panmictic population. Furthermore, we tested migration pathway to see the probable source and reciplent populations of first generation migrants in S. furcifera. In 2012, Laos, Nepal, Thailand, Vietnam and four different sites of Bangladesh showed the potential source of S. furcifera. In 2013, we observed S. furcifera in Korea was more likely originated from Nepal and Bangladesh. Various migration pathway showed in fifteen different sites of Korea as panmictic population. Lastly in 2014, the migration pathway indicated that S. furcifera migrates from China to Korea. Seemingly, S. furcifera in Asia display as large panmictic population and more study is acquire to verify the origin source.