Evidence map›Paper›PMID 31048459›Full record

ArticleScience (New York, N.Y.)2019

A compact synthetic pathway rewires cancer signaling to therapeutic effector release.

Hokyung K Chung, Xinzhi Zou, Bryce T Bajar, Veronica R Brand, Yunwen Huo, Javier F Alcudia, James E Ferrell, Michael Z Lin

Open access · greenAbstract read
In one paragraph

Article in Science (New York, N.Y.), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
2.2field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

35 citing papers in PubMed, 63 citations in OpenAlex.

  1. Article
  2. Programming T cells for intercellular genome editing.bioRxiv : the preprint server for biology · 2026
    Article
  3. Article
  4. Review
  5. Sensing and Reprogramming Surface Receptor Activation With Synthetic Transcriptional Circuits.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  6. Article
  7. Protein engineering: status report.Protein engineering, design & selection : PEDS · 2026
    Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Perspectives on Synthetic Protein Circuits in Mammalian Cells.Current opinion in biomedical engineering · 2024
    Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Synthetic Gene Circuits for Regulation of Next-Generation Cell-Based Therapeutics.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Hokyung K ChungDepartment of Biology, Stanford University, Stanford, CA, USA.ORCID 0000-0002-7028-2432
Xinzhi ZouDepartment of Bioengineering, Stanford University, Stanford, CA, USA.
Bryce T BajarDepartment of Pediatrics, Stanford University, Stanford, CA, USA.
Veronica R BrandDepartment of Pediatrics, Stanford University, Stanford, CA, USA.
Yunwen HuoDepartment of Neurobiology, Stanford University, Stanford, CA, USA.
Javier F AlcudiaNeuroscience Gene Vector and Virus Core, Stanford University, Stanford, CA, USA.
James E FerrellDepartment of Chemical and Systems Biology, Stanford University, Stanford, CA, USA.ORCID 0000-0003-4767-3926
Michael Z LinDepartment of Neurobiology, Stanford University, Stanford, CA, USA. mzlin@stanford.edu.ORCID 0000-0002-0492-1961
Stanford University · US

Funding

TRAINING & OUTREACH COREP50GM107615 · NIGMS · STANFORD UNIVERSITY · PI FERRELL, JAMES E. · 2013 to 2017
$10.9M
Cytoplasmic organization and systems-level function in Xenopus extractsR35GM131792 · NIGMS · STANFORD UNIVERSITY · PI JAMES E. FERRELL · 2019 to 2026
$5.6M
A Molecular Tag for Drug-Regulated Synthesis of Specific ProteinsR01GM098734 · NIGMS · STANFORD UNIVERSITY · PI LIN, MICHAEL Z. · 2011 to 2014
$1.2M
NIGMS NIH HHS P50 GM107615NIGMS NIH HHS R01 GM098734NIGMS NIH HHS R35 GM131792
6 · The paper itself

Abstract

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.

Indexed as

AdenoviridaeApoptosisBioengineeringCell Line, TumorCRISPR-Associated Protein 9CRISPR-Cas SystemsDEAD-box RNA HelicasesEndopeptidasesErb-b2 Receptor Tyrosine KinasesHumansModels, TheoreticalNeoplasmsNucleoside-TriphosphataseProtein StabilityProteolysisSerine EndopeptidasesCRISPR-Associated Protein 9DEAD-box RNA HelicasesEndopeptidasesERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesNS3 protein, hepatitis C virusNucleoside-TriphosphataseSerine EndopeptidasesTEV proteaseViral Nonstructural ProteinsViral Proteases

Identifiers

PMID31048459
PMCPMC7053279
OpenAlexW2942604302

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.