| Literature DB >> 30404655 |
Wuhua Zhou1,2,3,4,5, Li Gong6, Qinchuan Wu1,2,3,4,5, Chunyang Xing1, Bajin Wei2,3,4, Tianchi Chen1,2,3,4,5, Yuan Zhou1,2,3,4,5, Shengyong Yin2,3,4, Bin Jiang7, Haiyang Xie2,3,4,5, Lin Zhou8,9,10,11,12, Shusen Zheng13,14,15,16,17.
Abstract
In the publication of this article [1], there are two inadvertent errors.Entities:
Year: 2018 PMID: 30404655 PMCID: PMC6220448 DOI: 10.1186/s13046-018-0944-7
Source DB: PubMed Journal: J Exp Clin Cancer Res ISSN: 0392-9078
Fig. 2PHF8 knockdown significantly suppresses proliferation, migration, invasion and autophagy of HCC cells in vitro. a Determination of transfection efficiency of shRNAs targeting PHF8 in SMMC-7721 and Huh7 by qRT-PCR and western-blot assay. Scramble shRNA (shCtrl) was used for negative control. b Inhibited proliferation of SMMC-7721 and Huh7 cells in PHF8 knockdown group by CCK8 assasy (n = 6). c, d) Representative images and quantification of migrated and invasive cells by transwell assay in SMMC-7721 and Huh7 cells (n = 3, magnification, × 100). e Representative immunoblot results of autophagy markers, LC3B and p62 in SMMC-7721 and Huh7 cells with PHF8 knockdown. Both cell lines transfected with indicated shRNAs were cultured in complete medium with 10% FBS or EBSS starvation condition with or without CQ (100 μmol) for 8-h. The ratio of LC3-II to LC3-I and p62 to β-actin were shown at the bottom of each band (n = 3). f Representative fluorescence images of autophagosomes and autolysosomes in SMMC-7721 and Huh7 cells with PHF8 knockdown by tandem mCherry-GFP-LC3 fusion protein assay (magnification, × 400). g Quantification of autophagosomes and autolysosomes from random 5 high-power fields of the merged images of each group. * P < 0.05, ** P < 0.01, *** P < 0.001. Data were presented by mean ± SD