Evidence map›Paper›PMID 37563300›Full record

ArticleNature biotechnology2024

Generation of precision preclinical cancer models using regulated in vivo base editing.

Alyna Katti, Adrián Vega-Pérez, Miguel Foronda, Jill Zimmerman, Maria Paz Zafra, Elizabeth Granowsky, Sukanya Goswami, Eric E Gardner, Bianca J Diaz, Janelle M Simon and 9 more

Open access · greenAbstract read
In one paragraph

Article in Nature biotechnology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
4.3field-weighted citation impact, top 5% 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

24 citing papers in PubMed, 28 citations in OpenAlex.

  1. Trial
  2. Article
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  8. Genetic mechanisms of resistance to targeted KRAS inhibition.bioRxiv : the preprint server for biology · 2025
    Article
  9. Review
  10. Review
  11. The roles of arginases and arginine in immunity.Nature reviews. Immunology · 2025
    Review
  12. Article
  13. Article
  14. Review
  15. Review
  16. Review
  17. Article
  18. Review
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  20. Deconstructing cancer with precision genome editing.Biochemical Society transactions · 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

19 authors at 3 institutions in 2 countries.

Alyna Katti *Sandra and Edward Meyer Cancer Center, Weill Cornell Medicine, New York, NY, USA.
Adrián Vega-Pérez *Sandra and Edward Meyer Cancer Center, Weill Cornell Medicine, New York, NY, USA.
Miguel ForondaSandra and Edward Meyer Cancer Center, Weill Cornell Medicine, New York, NY, USA.ORCID http://orcid.org/0000-0001-9590-9281
Jill ZimmermanSandra and Edward Meyer Cancer Center, Weill Cornell Medicine, New York, NY, USA.
Maria Paz ZafraSandra and Edward Meyer Cancer Center, Weill Cornell Medicine, New York, NY, USA.
Elizabeth GranowskySandra and Edward Meyer Cancer Center, Weill Cornell Medicine, New York, NY, USA.
Sukanya GoswamiSandra and Edward Meyer Cancer Center, Weill Cornell Medicine, New York, NY, USA.
Eric E GardnerSandra and Edward Meyer Cancer Center, Weill Cornell Medicine, New York, NY, USA.ORCID http://orcid.org/0000-0002-1552-2675
Bianca J DiazSandra and Edward Meyer Cancer Center, Weill Cornell Medicine, New York, NY, USA.ORCID http://orcid.org/0000-0002-5309-1300
Janelle M SimonCancer Biology and Genetics, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Alexandra WuestCancer Biology and Genetics, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Wei LuanCancer Biology and Genetics, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Maria Teresa Calvo FernandezSandra and Edward Meyer Cancer Center, Weill Cornell Medicine, New York, NY, USA.
Anastasia P KadinaSynthego Corporation, Redwood City, CA, USA.
John A WalkerSynthego Corporation, Redwood City, CA, USA.
Kevin HoldenSynthego Corporation, Redwood City, CA, USA.ORCID http://orcid.org/0000-0002-3091-4124
Scott W LoweCancer Biology and Genetics, Memorial Sloan Kettering Cancer Center, New York, NY, USA.ORCID http://orcid.org/0000-0002-5284-9650
Francisco J Sánchez RiveraCancer Biology and Genetics, Memorial Sloan Kettering Cancer Center, New York, NY, USA.ORCID http://orcid.org/0000-0002-8466-8563
Lukas E DowSandra and Edward Meyer Cancer Center, Weill Cornell Medicine, New York, NY, USA. lud2005@med.cornell.edu.ORCID http://orcid.org/0000-0001-7048-1418
Cornell University · USMemorial Sloan Kettering Cancer Center · USSynthego (United States) · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Scientific ReagentsP01CA087497 · NCI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI CORDON-CARDO, CARLOS · 2000 to 2021
$35.4M
In Vivo Base Editing for Precision Oncology ModelsR01CA229773 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI DOW, LUKAS EDWARD · 2019 to 2023
$3.1M
Rapid and flexible precision oncology mouse models of epithelial malignancies epithelial malignanciesR01CA233944 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI LOWE, SCOTT W. · 2020 to 2024
$2.4M
Translational Research in Oncology Training ProgramT32CA160001 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI SAWYERS, CHARLES L. · 2011 to 2020
$2.0M
Interrogating the role of mutant KRAS allelic imbalance and co-mutated genes in targeted therapy response of NSCLCF31CA261061 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI DIAZ, BIANCA · 2021 to 2024
$189k
Sensitizing Colorectal Cancer to Checkpoint Inhibitors by WNT Pathway SuppressionF31CA247351 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI KATTI, ALYNA · 2020 to 2022
$127k
NCI NIH HHS F31 CA247351NCI NIH HHS F31 CA261061NCI NIH HHS P01 CA087497NCI NIH HHS P30 CA008748NCI NIH HHS R01 CA229773NCI NIH HHS R01 CA233944NCI NIH HHS T32 CA160001
6 · The paper itself

Abstract

Although single-nucleotide variants (SNVs) make up the majority of cancer-associated genetic changes and have been comprehensively catalogued, little is known about their impact on tumor initiation and progression. To enable the functional interrogation of cancer-associated SNVs, we developed a mouse system for temporal and regulatable in vivo base editing. The inducible base editing (iBE) mouse carries a single expression-optimized cytosine base editor transgene under the control of a tetracycline response element and enables robust, doxycycline-dependent expression across a broad range of tissues in vivo. Combined with plasmid-based or synthetic guide RNAs, iBE drives efficient engineering of individual or multiple SNVs in intestinal, lung and pancreatic organoids. Temporal regulation of base editor activity allows controlled sequential genome editing ex vivo and in vivo, and delivery of sgRNAs directly to target tissues facilitates generation of in situ preclinical cancer models.

Indexed as

Gene EditingNeoplasmsAnimalsCRISPR-Cas SystemsLungMiceRNA, Guide, CRISPR-Cas SystemsRNA, Guide, CRISPR-Cas Systems

Identifiers

PMID37563300
PMCPMC11295146
OpenAlexW4385741654

What OpenQuestion holds

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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.