4.8 Article

SYNTHETIC BIOLOGY A compact synthetic pathway rewires cancer signaling to therapeutic effector release

Journal

SCIENCE
Volume 364, Issue 6439, Pages 451-+

Publisher

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/science.aat6982

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Funding

  1. Stanford Graduate Fellowship
  2. Ilju Foundation Predoctoral Scholarship
  3. NIH/NIGMS EUREKA grant [5R01GM098734]
  4. Burroughs Wellcome Foundation Career Award for Medical Scientists
  5. Alliance for Cancer Gene Therapy Young Investigator Award
  6. NIH/NIGMS center grant [P50GM107615]
  7. Damon Runyon-Rachleff Innovation award

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An important goal in synthetic biology is to engineer biochemical pathways to address unsolved biomedical problems. One long-standing problem in molecular medicine is the specific identification and ablation of cancer cells. Here, we describe a method, named Rewiring of Aberrant Signaling to Effector Release (RASER), in which oncogenic ErbB receptor activity, instead of being targeted for inhibition as in existing treatments, is co-opted to trigger therapeutic programs. RASER integrates ErbB activity to specifically link oncogenic states to the execution of desired outputs. A complete mathematical model of RASER and modularity in design enable rational optimization and output programming. Using RASER, we induced apoptosis and CRISPR-Cas9-mediated transcription of endogenous genes specifically in ErbB-hyperactive cancer cells. Delivery of apoptotic RASER by adeno-associated virus selectively ablated ErbB-hyperactive cancer cells while sparing ErbB-normal cells. RASER thus provides a new strategy for oncogene-specific cancer detection and treatment.

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