Skip to main navigation Skip to search Skip to main content

Potentiation of paclitaxel activity by curcumin in human breast cancer cell by modulating apoptosis and inhibiting EGFR signaling

  • Yingzhuan Zhan
  • , Yinnan Chen
  • , Rui Liu
  • , Han Zhang
  • , Yanmin Zhang

Research output: Contribution to journalArticlepeer-review

104 Scopus citations

Abstract

It has been suggested that combined effect of natural products may improve the treatment effectiveness in combating proliferation of cancer cells. Here, we examined the combined anticancer activities of compounds of three natural origin including baicalein, curcumin, and resveratrol with chemotherapy drug paclitaxel respectively, which showed that combination of paclitaxel with curcumin exhibited synergistic growth inhibition and induced significant apoptosis in MCF-7 cell lines. Treatment of MCF-7 cell lines with paclitaxel and curcumin induced the apoptosis of regulatory protein Bcl-2 but decreased Bax expression. In addition, simultaneous treatment with paclitaxel and curcumin strongly inhibited paclitaxel-induced activities of EGFR signaling. Furthermore, the combination of paclitaxel and curcumin exerted increased anti-tumor efficacy on mouse models. Overall, our data described the promising therapeutic potential and underlying mechanisms of combining paclitaxel with curcumin in treating breast cancer.

Original languageEnglish
Pages (from-to)1086-1095
Number of pages10
JournalArchives of Pharmacal Research
Volume37
Issue number8
DOIs
StatePublished - Aug 2014

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Apoptosis
  • Breast cancer
  • EGFR signaling
  • Natural products
  • Paclitaxel
  • Synergism

Fingerprint

Dive into the research topics of 'Potentiation of paclitaxel activity by curcumin in human breast cancer cell by modulating apoptosis and inhibiting EGFR signaling'. Together they form a unique fingerprint.

Cite this