
==== Front
Int J Oncol
Int J Oncol
IJO
International Journal of Oncology
1019-6439
1791-2423
D.A. Spandidos

10.3892/ijo.2024.5683
ijo-65-04-05683
Corrigendum
[Corrigendum] (-)-Epigallocatechingallate induces apoptosis in B lymphoma cells via caspase-dependent pathway and Bcl-2 family protein modulation
Wang Jiangyan
Xie Yu'an
Feng Yan
Zhang Litu
Huang Xinping
Shen Xiaoyun
Luo Xiaoling
10 2024
28 8 2024
28 8 2024
65 4 95Copyright: © 2024 Wang et al.
2024
https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
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pmcInt J Oncol 46: 1507-1515, 2015; DOI: 10.3892/ijo.2015.2869

Subsequently to the publication of the above article, an interested reader drew to the authors' attention that, in Fig. 3 on p. 1510, the western blot images selected to portray the caspase 7 and PARP/cleaved PARP experiments were remarkably similar.

After having referred to their original data, the authors realized that the PARP/cleaved PARP blots had been inadvertently duplicated in the figure. The revised version of Fig. 3, showing the correct data for the caspase-7 experiment, is shown below. The authors confirm that the errors made during the assembly of Fig. 3 did not adversely affect the major conclusions presented in this paper, and are grateful to the Editor of International Journal of Oncology for allowing them this opportunity to publish a corrigendum. They also apologize to the readership for any inconvenience caused.

Figure 3 EGCG increases the activation of caspase-3, -7 and PARP. (A) Jeko-1 or Raji cells were treated with EGCG at different concentrations (0, 20, 40 and 60 μg/ml) for 24 h. Equal amounts of total protein were examined by western blot analysis with indicated antibodies. β-actin was used as a loading control. Representative data from three independent experiments are shown. (B) Relative intensity of cleaved caspase-3, -7 and PARP, normalized by uncleaved caspase-3, -7 and PARP. Values represent mean ± SD from three independent experiments. *p<0.05, compared with control cells (0 μg/ml).
