Pulsed-wave Ultrasound Hyperthermia Enhanced Nanodrug Delivery Combined with Chloroquine Exerts Effective Antitumor Response and Postpones Recurrence

Sci Rep. 2019 Aug 28;9(1):12448. doi: 10.1038/s41598-019-47345-8.

Abstract

Autophagy is found to serve as a surviving mechanism for cancer cells. Inhibiting autophagy has been considered as an adjuvant anti-cancer strategy. In this study, we investigated the anti-tumor effect of combining pulsed-wave ultrasound hyperthermia (pUH) enhanced PEGylated liposomal doxorubicin (PLD) delivery with an autophagy inhibitor chloroquine (CQ). BALB/c mice bearing subcutaneous 4T1 tumor received intravenous injection of PLD (10 mg/kg) plus 15-minute on-tumor pUH on Day 5 after tumor implantation and were then fed with CQ (50 mg/kg daily) thereafter. Prolonged suppression of tumor growth was attained with PLD + pUH + CQ treatment, whereas in PLD + pUH group tumors quickly recurred after an initial inhibition. Treatment with CQ monotherapy had no benefit compared to the control group. Immunohistochemical staining and Western blotting showed that autophagy of cancer cells was blocked for the mice receiving CQ. It indicates that PLD + pUH + CQ is a promising strategy to treat cancer for a long-term inhibition.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line, Tumor
  • Chloroquine / pharmacology
  • Doxorubicin* / pharmacology
  • Drug Delivery Systems*
  • Female
  • Hyperthermia, Induced*
  • Mammary Neoplasms, Experimental* / immunology
  • Mammary Neoplasms, Experimental* / pathology
  • Mammary Neoplasms, Experimental* / therapy
  • Mice
  • Mice, Inbred BALB C
  • Nanoparticles / therapeutic use*
  • Ultrasonic Waves*

Substances

  • Doxorubicin
  • Chloroquine