Open Access

(-)-Epigallocatechingallate induces apoptosis in B lymphoma cells via caspase-dependent pathway and Bcl-2 family protein modulation

Corrigendum in: /10.3892/ijo.2024.5683

  • Authors:
    • Jiangyan Wang
    • Yu'an Xie
    • Yan Feng
    • Litu Zhang
    • Xinping Huang
    • Xiaoyun Shen
    • Xiaoling Luo
  • View Affiliations

  • Published online on: February 3, 2015     https://doi.org/10.3892/ijo.2015.2869
  • Pages: 1507-1515
  • Copyright: © Wang et al. This is an open access article distributed under the terms of Creative Commons Attribution License [CC BY_NC 3.0].

Metrics: Total Views: 0 (Spandidos Publications: | PMC Statistics: )
Total PDF Downloads: 0 (Spandidos Publications: | PMC Statistics: )


Abstract

(-)-Epigallocatechingallate (EGCG) as a representative polyphenol has attracted increasing attention due to its diversified effects, especially its potential as an agent for the prevention or treatment of certain cancers. However, the molecular mechanisms of EGCG-induced apoptosis in B lymphoma cells are unclear. The aim of this study was to investigate the effect of EGCG on proliferation and apoptosis in the B lymphoma cell lines Jeko-1 and Raji, and determine the underlying mechanisms. Cell proliferation and cytotoxicity were determined by the cell counting kit (CCK-8) assay; apoptosis was assessed by flow cytometry using the Annexin V-PE/7AAD double staining; Fas, Bcl-2 and Bax mRNA expression levels were determined by real-time PCR; caspase activity was measured by the caspase activity assay kit; the expression levels of apoptosis-associated proteins were determined by western blot analysis. We demonstrated that EGCG induced growth inhibition and apoptosis in a dose- and time-dependent manner. In agreement, EGCG upregulated the mRNA expression of Fas and Bax while downregulating Bcl-2. Protein expression levels of Bax, activated caspase-3, -7, -8, and -9, and PARP were increased, while Bcl-2 protein levels were reduced by EGCG treatment. Taken together, EGCG induces B lymphoma cell apoptosis by triggering caspase-dependent intrinsic (mitochondrial) and extrinsic (death receptor) pathways. These findings suggest that EGCG may be a potential agent for the treatment of B lymphoma.
View Figures
View References

Related Articles

Journal Cover

April-2015
Volume 46 Issue 4

Print ISSN: 1019-6439
Online ISSN:1791-2423

Sign up for eToc alerts

Recommend to Library

Copy and paste a formatted citation
x
Spandidos Publications style
Wang J, Xie Y, Feng Y, Zhang L, Huang X, Shen X and Luo X: (-)-Epigallocatechingallate induces apoptosis in B lymphoma cells via caspase-dependent pathway and Bcl-2 family protein modulation Corrigendum in /10.3892/ijo.2024.5683. Int J Oncol 46: 1507-1515, 2015.
APA
Wang, J., Xie, Y., Feng, Y., Zhang, L., Huang, X., Shen, X., & Luo, X. (2015). (-)-Epigallocatechingallate induces apoptosis in B lymphoma cells via caspase-dependent pathway and Bcl-2 family protein modulation Corrigendum in /10.3892/ijo.2024.5683. International Journal of Oncology, 46, 1507-1515. https://doi.org/10.3892/ijo.2015.2869
MLA
Wang, J., Xie, Y., Feng, Y., Zhang, L., Huang, X., Shen, X., Luo, X."(-)-Epigallocatechingallate induces apoptosis in B lymphoma cells via caspase-dependent pathway and Bcl-2 family protein modulation Corrigendum in /10.3892/ijo.2024.5683". International Journal of Oncology 46.4 (2015): 1507-1515.
Chicago
Wang, J., Xie, Y., Feng, Y., Zhang, L., Huang, X., Shen, X., Luo, X."(-)-Epigallocatechingallate induces apoptosis in B lymphoma cells via caspase-dependent pathway and Bcl-2 family protein modulation Corrigendum in /10.3892/ijo.2024.5683". International Journal of Oncology 46, no. 4 (2015): 1507-1515. https://doi.org/10.3892/ijo.2015.2869