Skip to main content

Correction: CircZNF215 promotes tumor growth and metastasis through inactivation of the PTEN/AKT pathway in intrahepatic cholangiocarcinoma

The Original Article was published on 18 May 2023

Correction: J Exp Clin Cancer Res 42, 125 (2023)

https://doi.org/10.1186/s13046-023-02699-w

Following the publication of the original article [1], the authors identified errors in the body. Under the Results, the last paragraph of CircZNF215 is considerably increased in iCCA tissues, and high expression of cZNF215 is correlated with metastasis and poor prognosis in iCCA patients section should be corrected. The updated sentence is given below and the error found in original sentence have been highlighted in bold typeface.

There are several statistical data errors in the article due to author's carelessness. Although these errors do not affect the final conclusions, they should be corrected for the sake of the rigor of scientific research.

Original sentence

In multivariate regression analysis, multiple tumor number, poorer tumor diferentiation, larger tumor size, and high cZNF215 expression were independent risk factors for OS, while the presence of MVI, poorer tumor diferentiation, advanced TNM stage and higher cZNF215 expression were regarded as independent risk factors for RFS (Fig.1H, Supporting Table S2).

Incorrect Figure 1

Fig. 1
figure 1

High expression of cZNF215 is correlated with iCCA metastasis and poor patient prognosis. A Clustered heat map of all diferentially expressed circRNAs in 15 iCCA tissues with and without extrahepatic metastasis, respectively. B Volcano plot compared the expression fold changes of circRNAs for iCCA tissues with extrahepatic metastases versus without extrahepatic metastases. C Quantitative real-time PCR analysis showed that the levels of cZNF215 expression were the highest among the 4 upregulated circRNAs in RBE, HuCCT1, and HCCC9810 cell lines. D Schematic illustration of cZNF215 locus with specifc primers and Sanger sequencing result of cZNF215. E qRT-PCR to detect the expression of cZNF215 in 51 iCCA tissues and paired normal tissues. F Relative RNA levels of cZNF215 in iCCA tissues (n = 15) with and without extrahepatic metastasis, respectively. G Kaplan–Meier analysis showing the association of cZNF215 expression with OS or RFS in iCCA tissues. H Multivariate analysis of OS and RFS prognostic indicators. Data represent means ± SD of at least three independent experiments

Updated sentence

In multivariate regression analysis, multiple tumor number, poorer tumor differentiation, larger tumor size, and high cZNF215 expression were independent risk factors for OS, while the poorer tumor differentiation, advanced TNM stage and higher cZNF215 expression were regarded as independent risk factors for RFS (Corrected Fig. 1H, Corrected Table S2).

Furthermore, Fig. 1H and Supplementary Table 2 should also be corrected. The corrected figure is given below. The original article has been corrected.

Corrected Figure 1

Fig. 1
figure 2

High expression of cZNF215 is correlated with iCCA metastasis and poor patient prognosis. A Clustered heat map of all diferentially expressed circRNAs in 15 iCCA tissues with and without extrahepatic metastasis, respectively. B Volcano plot compared the expression fold changes of circRNAs for iCCA tissues with extrahepatic metastases versus without extrahepatic metastases. C Quantitative real-time PCR analysis showed that the levels of cZNF215 expression were the highest among the 4 upregulated circRNAs in RBE, HuCCT1, and HCCC9810 cell lines. D Schematic illustration of cZNF215 locus with specifc primers and Sanger sequencing result of cZNF215. E qRT-PCR to detect the expression of cZNF215 in 51 iCCA tissues and paired normal tissues. F Relative RNA levels of cZNF215 in iCCA tissues (n = 15) with and without extrahepatic metastasis, respectively. G Kaplan–Meier analysis showing the association of cZNF215 expression with OS or RFS in iCCA tissues. H Multivariate analysis of OS and RFS prognostic indicators. Data represent means ± SD of at least three independent experiments

Reference

  1. Liao W, Du J, Li L, et al. CircZNF215 promotes tumor growth and metastasis through inactivation of the PTEN/AKT pathway in intrahepatic cholangiocarcinoma. J Exp Clin Cancer Res. 2023;42:125. https://doi.org/10.1186/s13046-023-02699-w.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding authors

Correspondence to Kefei Yuan or Yong Zeng.

Supplementary Information

Additional file 1:

 Corrected table S2. Multivariate analysis of several variables for OS and RFS.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Liao, W., Du, J., Li, L. et al. Correction: CircZNF215 promotes tumor growth and metastasis through inactivation of the PTEN/AKT pathway in intrahepatic cholangiocarcinoma. J Exp Clin Cancer Res 43, 55 (2024). https://doi.org/10.1186/s13046-024-02977-1

Download citation

  • Published:

  • DOI: https://doi.org/10.1186/s13046-024-02977-1