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. 2018 May 23;18(1):779–788. doi: 10.3892/mmr.2018.9058

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Copyright: © Qu et al.

This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.

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Figure 4. — Proliferation, migration and invasion of MG63 cells are suppressed following transfection with pcDNA WWOX-AS1 (magnification, ×200). (A) Proliferation of MG63 cells transfected pcDNA WWOX-AS1 was significantly decreased compared with the pcDNA control group. (B) Scratch wound healing assays revealed that migration of MG63 cells transfected with pcDNA WWOX-AS1 was significantly suppressed compared with the pcDNA control group. (C) Matrigel invasion assays revealed that the invasion of MG63 cells transfected with pcDNA WWOX-AS1 was significantly suppressed compared with the pcDNA control group. *P<0.05 vs. the pcDNA control group. WWOX, WW domain-containing oxidoreductase; WWOX-AS1, WWOX antisense RNA 1; pcDNA, plasmid complementary DNA.

Figure 4. — Proliferation, migration and invasion of MG63 cells are suppressed following transfection with pcDNA WWOX-AS1 (magnification, ×200). (A) Proliferation of MG63 cells transfected pcDNA WWOX-AS1 was significantly decreased compared with the pcDNA control group. (B) Scratch wound healing assays revealed that migration of MG63 cells transfected with pcDNA WWOX-AS1 was significantly suppressed compared with the pcDNA control group. (C) Matrigel invasion assays revealed that the invasion of MG63 cells transfected with pcDNA WWOX-AS1 was significantly suppressed compared with the pcDNA control group. *P<0.05 vs. the pcDNA control group. WWOX, WW domain-containing oxidoreductase; WWOX-AS1, WWOX antisense RNA 1; pcDNA, plasmid complementary DNA.