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Wang J, Li H, Xia C, et al. Onco Targets Ther. 2019;12:869–882.
The authors have suggested Determine 2E on web page 874 is inaccurate. As a result of an error on the time of determine meeting NC (24 h) and shCENPK (48 h) within the SMMC-7721 row had been inadvertently duplicated. The right Determine 2 is as follows.
Determine 2 Silencing of CENPK inhibits HCC cell development, migration, and invasion in vitro.
Abbreviations: qRT-PCR, quantitative real-time PCR; CCK-8, Cell Counting Package-8; NC, adverse management.
Notes: (A) Expression of CENPK in BEL-7404 and SMMC-7721 cells was confirmed by qRT-PCR and Western blotting after transfection with shCENPK lentivirus or shNC. (B) Proliferation fee of BEL-7404 and SMMC-7721 cells was measured over 4 days by the CCK-8 assay. (C and D) Consultant photographs (C) and quantification (D) of the colony formation assays are proven for BEL-7404 and SMMC-7721 cells. (E) Evaluation of migration in BEL-7404 and SMMC-7721 cells as measured by wound therapeutic assays (×200). (F and G) Evaluation of invasion in BEL-7404 and SMMC-7721 cells as measured by transwell assays. (F) Consultant images (×200). (G) Variety of invaded cells was counted in 5 randomly chosen areas. Scale bar =100 μm. NC represents adverse management group (shNC), and shCENPK represents downregulation of CENPK group. *P<0.05, **P<0.01, ***P<0.001.
The authors apologize for this error and advise it doesn’t have an effect on the outcomes of the paper.
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