* p ≤ 0.05, ** p ≤ 0.01, *** p ≤ 0.005 indicated statistical significance. PLX-4720 solubility dmso Data are presented as mean ± standard deviation. Each experiment was repeated at least three times. Multiple group comparison experiments were validated by ANOVA. Results Single cell cloning Four clones were isolated from the pancreatic cell line, MiaPaCa-2 and successfully established as cell lines.

The invasion status of the clones was tested using the Boyden chamber assay with inserts coated with matrigel. Two sub-populations, Clone #3 and Clone #8, showed a significant Selleckchem RGFP966 increase (Clone #3, 2.5-fold increase, p = 0.001) and decrease (Clone #8, 12-fold decrease, p = 0.00001), ANOVA (p < 0.001), (Fig 1A(i-ii) and 1B) in invasion through matrigel, compared to the parental MiaPaCa-2 cells. These two

clonal populations also displayed distinct morphological differences (Fig 1A(iii-iv)). The invasive cell line, Clone #3 displayed an elongated spindled shaped click here morphology, similar to mesenchymal cells. Clone #8, low invasion, was similar to epithelial cells in tight clustered colonies. Figure 1 A. Morphology of the highly invasive (i) Clone #3 with elongated and spindle-like phenotype and low-invasive (ii) Clone #8 with epithelial tight colonies. Cell invasion assay representing (iii) Clone #3 and (iv) Clone #8 invading through ECM coated Boyden chamber, stained with crystal violet. Magnification 200×. Scale bar, 200 μm. B. Total number of invading cells. Results shown are a minimum of three repeats ± standard deviation (n = 3). Invasion and adhesion to ECM proteins Invasion of MiaPaCa-2 and sub-populations, Clone #3 and Clone #8, through a range of ECM proteins was examined (Fig 2A). The selleck invasion

of MiaPaCa-2 and Clone #3 is comparable through laminin and fibronectin whereas Clone #8 showed a significant decrease in invasion, 6.3 and 4.0-fold (p = 0.002, p = 0.008) through laminin and fibronectin, respectively, ANOVA (all p < 0.001). Low invasion was observed for Clone #3 through collagens type I and IV; Clone #8 showed significantly decreased invasion through the collagens (1.6 and 1.6-fold (p = 0.03, p = 0.02)), ANOVA (p = 0.007, p = 0.001). Interestingly, the lowest level of invasion displayed by the cell lines was through the collagens, type IV and I, which is in agreement with previous studies indicating MiaPaCa-2 does not express collagen-binding integrins [23]. The highest level of invasion was observed through fibronectin. Clone #3 also displayed significantly increased motility (p = 0.00005) whereas the motility of Clone #8 was similar to that of MiaPaCa-2, ANOVA (p < 0.001) (Fig 2A). Figure 2 A. Invasion assay of MiaPaCa-2, Clone #3 and Clone #8 through ECM proteins. Motility assay refers to invasion assay without the presence of ECM. Results are displayed as the total mean number of cells invading at 200× magnification (n = 3). B.