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Augmenting Tumor-Starvation Therapy by Cancer Cell Autophagy Inhibition

  • Bowen Yang
  • , Li Ding
  • , Yu Chen*
  • , Jianlin Shi
  • *Corresponding author for this work
  • CAS - Shanghai Institute of Ceramics
  • University of Chinese Academy of Sciences

Research output: Contribution to journalArticlepeer-review

Abstract

It was recently recognized that cancer therapeutic efficacy may be greatly compromised by an intrinsic protective mechanism called autophagy, by which cancer cells survive in harsh conditions such as starvation. Here, a synergetic strategy is described for cancer treatment by suppressing such a protective mechanism for augmenting tumor-starvation therapy. The synergetic therapy is achieved by restraining glucose metabolism using an antiglycolytic agent to predispose cancer cells to severe energy deprivation; concurrently the downstream autophagic flux and compensatory energy supplies are blocked by the autophagy inhibitor black phosphorus nanosheet. Cancer cells fail to extract their own nutrient to feed themselves, finally succumbing to therapeutic interventions and starving to death. Both in vitro and in vivo results evidence the cooperative effect between the autophagy inhibitor and antiglycolytic agent, which leads to remarkable synergetic antineoplastic outcome. It is expected that such a combinational approach by concurrently blocking exogenous and endogenous nutrition supplies will be beneficial to the design of effective tumor-specific cancer therapies in the future.

Original languageEnglish
Article number1902847
JournalAdvanced Science
Volume7
Issue number6
DOIs
StatePublished - 1 Mar 2020
Externally publishedYes

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

  • autophagy
  • black phosphorus
  • glycolysis
  • nanomedicine
  • tumor-starvation therapy

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