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Figure 7: Repressive effect of sh-VPS9D1-AS1 on malignant phenotypes of prostate cancer cells was rescued through upregulating fibroblast growth factor-like-1 (FGFRL1). (a) Quantitative real-time reverse transcription polymerase chain reaction was utilized to examine FGFRL1 level in PC-3 cells of 4 groups (sh-NC + oe-NC, sh-VPS9D1-AS1 + oe-NC, sh-NC + oe-FGFRL1, and sh-VPS9D1-AS1 + oe-FGFRL1). (b) Western blot was employed for measuring FGFRL1 protein level in PC-3 cells of 4 groups. (c) MTT was done to test the proliferative ability of PC-3 cells in 4 groups. (d) Colony formation assay was conducted for evaluating the colony formation property of PC-3 cells in 4 groups. (e) A wound healing assay was introduced for examination of the migratory capacity of PC-3 cells in 4 groups (magnification: ×40). (f) Cell invasion assay was launched for testing the invasive capacity of PC-3 cells in 4 groups (magnification: ×100). *P < 0.05 relative to sh-NC + oe-NC group, #P < 0.05 relative to sh-NC + oe-FGFRL1 group, n = 3. |
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