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. 2026 Feb 9;23:36. doi: 10.1186/s12985-026-03083-8

Correction: Hepatitis B virus x protein induces epithelial-mesenchymal transition of hepatocellular carcinoma cells by regulating long non-coding RNA

Yinji Jin 1,#, Di Wu 2,#, Weiwei Yang 1, Mingjiao Weng 1, Yafei Li 1, Xuefei Wang 1, Xiao Zhang 1, Xiaoming Jin 1,✉, Tianzhen Wang 1,✉
PMCID: PMC12884613  PMID: 41664161

Correction: Virology Journal (2017) 14(1):238

10.1186/s12985-017-0903-5

In this article [1], the wrong figure appeared as Fig. 3(b); the figure should have appeared as shown below.

Fig. 3.

Fig. 3

ZEB2-AS1 was an important lncRNA that mediated HBx-induced EMT. a The level of ZEB2-AS1 was verified by a real-time PCR assay. The siRNA can effectively inhibit the level of ZEB2-AS1. b Transwell assay. Knockdown of ZEB2-AS1 inhibited the metastatic ability of HepG2 cells. c. The level of ZEB2-AS1 was verified by a real-time PCR assay. ZEB2-AS1 was up-regulated by 3.79-fold by HBx, but compromised by si-ZEB2-AS1 in HepG2-HBx. d and e The regulating effect of ZEB2-AS1 on EMT was assessed by transwell assay. HBx promoted the metastatic ability of HCC cells; however, siRNA treatment against ZEB2-AS1 rescued the phenotype in these cells. f EMT markers were detected by Western blot. HBx overexpression enhanced vimentin and ZEB2 expression, whereas it inhibited E-cadherin expression. However, knockdown ZEB2-AS1 reversed the above protein expression. *p < 0.05, **p < 0.01

Incorrect version of Fig. 3b

Correct version of Fig. 3b

Fig. 3.

Fig. 3

ZEB2-AS1 was an important lncRNA that mediated HBx-induced EMT. a The level of ZEB2-AS1 was verified by a real-time PCR assay. The siRNA can effectively inhibit the level of ZEB2-AS1. b Transwell assay. Knockdown of ZEB2-AS1 inhibited the metastatic ability of HepG2 cells. c. The level of ZEB2-AS1 was verified by a real-time PCR assay. ZEB2-AS1 was up-regulated by 3.79-fold by HBx, but compromised by si-ZEB2-AS1 in HepG2-HBx. d and e The regulating effect of ZEB2-AS1 on EMT was assessed by transwell assay. HBx promoted the metastatic ability of HCC cells; however, siRNA treatment against ZEB2-AS1 rescued the phenotype in these cells. f EMT markers were detected by Western blot. HBx overexpression enhanced vimentin and ZEB2 expression, whereas it inhibited E-cadherin expression. However, knockdown ZEB2-AS1 reversed the above protein expression. *p < 0.05, **p < 0.01

Footnotes

Publisher’s note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Yinji Jin and Di Wu contributed equally to this work.

Contributor Information

Xiaoming Jin, Email: Jinxm55@163.com.

Tianzhen Wang, Email: wtzpath@163.com.

Reference

  • 1.Jin Yinji, Di Wu, Yang Weiwei, et al. Hepatitis B virus x protein induces epithelial-mesenchymal transition ofhepatocellular carcinoma cells by regulating long non-coding RNA. Virology Journal. 2027;14(1):56. 10.1186/s12985-017-0903-5. [DOI] [PMC free article] [PubMed] [Google Scholar]

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