Sonogenetics-controlled synthetic designer cells for cancer therapy in tumor mouse models

  • Tian Gao
  • , Lingxue Niu
  • , Xin Wu
  • , Di Dai
  • , Yang Zhou
  • , Mengyao Liu
  • , Ke Wu
  • , Yuanhuan Yu
  • , Ningzi Guan*
  • , Haifeng Ye*
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

31 Scopus citations

Abstract

Bacteria-based therapies are powerful strategies for cancer therapy, yet their clinical application is limited by a lack of tunable genetic switches to safely regulate the local expression and release of therapeutic cargoes. Rapid advances in remote-control technologies have enabled precise control of biological processes in time and space. We developed therapeutically active engineered bacteria mediated by a sono-activatable integrated gene circuit based on the thermosensitive transcriptional repressor TlpA39. Through promoter engineering and ribosome binding site screening, we achieved ultrasound (US)-induced protein expression and secretion in engineered bacteria with minimal noise and high induction efficiency. Specifically, delivered either intratumorally or intravenously, engineered bacteria colonizing tumors suppressed tumor growth through US-irradiation-induced release of the apoptotic protein azurin and an immune checkpoint inhibitor, a nanobody targeting programmed death-ligand 1, in different tumor mouse models. Beyond developing safe and high-performance designer bacteria for tumor therapy, our study illustrates a sonogenetics-controlled therapeutic platform that can be harnessed for bacteria-based precision medicine.

Original languageEnglish
Article number101513
JournalCell Reports Medicine
Volume5
Issue number5
DOIs
StatePublished - 21 May 2024

Keywords

  • PD-L1 nb
  • TlpA39
  • VNP20009
  • azurin
  • bacteria-based therapy
  • cancer therapy
  • sonogenetics
  • synthetic designer cells
  • synthetic gene circuit
  • ultrasound

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