Research Article

Long Noncoding RNA TUG1 Promotes the Function in ox-LDL-Treated HA-VSMCs via miR-141-3p/ROR2 Axis

Figure 2

Knockdown of TUG1 suppressed proliferation, migration, invasion, and the expression of metastasis-associated proteins in ox-LDL-stimulated HA-VSMCs in vitro. The HA-VSMCs were transfected with sh-NC or sh-TUG1. (a) Identification in knockdown efficiency of TUG1 was analyzed by qRT-PCR. (b) The cell viability at determined times (24 h, 48 h, and 72 h) was analyzed by MTT assay in ox-LDL-stimulated HA-VSMCs. (c) The levels of proliferation-related proteins Ki-67 and CyclinD1 were confirmed by western blot. (d, e) The cell migration and invasion were evaluated by transwell assay. (f) The western blot assay was used to detect the expression of metastasis-associated proteins, β-catenin, and Vimentin .
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