Harnessing copper-palladium alloy tetrapod nanoparticle-induced pro-survival autophagy for optimized photothermal therapy of drug-resistant cancer

Nat Commun. 2018 Oct 12;9(1):4236. doi: 10.1038/s41467-018-06529-y.

Abstract

Chemo-PTT, which combines chemotherapy with photothermal therapy, offers a viable approach for the complete tumor eradication but would likely fail in drug-resistant situations if conventional chemotherapeutic agents are used. Here we show that a type of copper (Cu)-palladium (Pd) alloy tetrapod nanoparticles (TNP-1) presents an ideal solution to the chemo-PTT challenges. TNP-1 exhibit superior near-infrared photothermal conversion efficiency, thanks to their special sharp-tip structure, and induce pro-survival autophagy in a shape- and composition-dependent manner. Inhibition of autophagy with 3-methyl adenine or chloroquine has a remarkable synergistic effect on TNP-1-mediated PTT in triple-negative (4T1), drug-resistant (MCF7/MDR) and patient-derived breast cancer models, achieving a level of efficacy unattainable with TNP-2, the identically-shaped CuPd nanoparticles that have a higher photothermal conversion efficiency but no autophagy-inducing activity. Our results provide a proof-of-concept for a chemo-PTT strategy, which utilizes autophagy inhibitors instead of traditional chemotherapeutic agents and is particularly useful for eradicating drug-resistant cancer.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alloys / chemistry*
  • Alloys / pharmacology*
  • Alloys / therapeutic use
  • Animals
  • Apoptosis / drug effects
  • Autophagy / drug effects*
  • Blotting, Western
  • Breast Neoplasms / drug therapy
  • Breast Neoplasms / metabolism
  • Cell Survival / drug effects
  • Copper / chemistry*
  • Drug Resistance, Neoplasm
  • Female
  • HeLa Cells
  • Humans
  • In Situ Nick-End Labeling
  • MCF-7 Cells
  • Mice
  • Mice, Inbred BALB C
  • Mice, SCID
  • Nanoparticles / chemistry*
  • Nanoparticles / therapeutic use*
  • Palladium / chemistry*
  • Phototherapy / methods*
  • Reactive Oxygen Species / metabolism

Substances

  • Alloys
  • Reactive Oxygen Species
  • Palladium
  • Copper