International Journal of Molecular Sciences (Feb 2022)

Modulatory Effects of Biosynthesized Gold Nanoparticles Conjugated with Curcumin and Paclitaxel on Tumorigenesis and Metastatic Pathways—In Vitro and In Vivo Studies

  • Satish Kumar Vemuri,
  • Satyajit Halder,
  • Rajkiran Reddy Banala,
  • Hari Krishnreddy Rachamalla,
  • Vijaya Madhuri Devraj,
  • Chandra Shekar Mallarpu,
  • Uttam Kumar Neerudu,
  • Ravikiran Bodlapati,
  • Sudip Mukherjee,
  • Subbaiah Goli Peda Venkata,
  • Gurava Reddy Annapareddy Venkata,
  • Malarvilli Thakkumalai,
  • Kuladip Jana

DOI
https://doi.org/10.3390/ijms23042150
Journal volume & issue
Vol. 23, no. 4
p. 2150

Abstract

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Background: Breast cancer is the most common cancer in women globally, and diagnosing it early and finding potential drug candidates against multi-drug resistant metastatic breast cancers provide the possibilities of better treatment and extending life. Methods: The current study aimed to evaluate the synergistic anti-metastatic activity of Curcumin (Cur) and Paclitaxel (Pacli) individually, the combination of Curcumin–Paclitaxel (CP), and also in conjugation with gold nanoparticles (AuNP–Curcumin (Au-C), AuNP–Paclitaxel (Au-P), and AuNP–Curcumin–Paclitaxel (Au-CP)) in various in vitro and in vivo models. Results: The results from combination treatments of CP and Au-CP demonstrated excellent synergistic cytotoxic effects in triple-negative breast cancer cell lines (MDA MB 231 and 4T1) in in vitro and in vivo mouse models. Detailed mechanistic studies were performed that reveal that the anti-cancer effects were associated with the downregulation of the expression of VEGF, CYCLIN-D1, and STAT-3 genes and upregulation of the apoptotic Caspase-9 gene. The group of mice that received CP combination therapy (with and without gold nanoparticles) showed a significant reduction in the size of tumor when compared to the Pacli alone treatment and control groups. Conclusions: Together, the results suggest that the delivery of gold conjugated Au-CP formulations may help in modulating the outcomes of chemotherapy. The present study is well supported with observations from cell-based assays, molecular and histopathological analyses.

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