Evidence map›Paper›PMID 41733988›Full record

ArticleeLife2026

Synthetic gene circuits that selectively target RAS-driven cancers.

Gabriel Valentin Senn, Leon Nissen, Yaakov Benenson

Abstract read
In one paragraph

Article in eLife, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

3 authors.

Gabriel Valentin SennDepartment of Biosystems Science and Engineering, ETH Zurich, Basel, Switzerland.ORCID https://orcid.org/0009-0002-7123-2899
Leon NissenDepartment of Biosystems Science and Engineering, ETH Zurich, Basel, Switzerland.ORCID https://orcid.org/0009-0009-3272-834X
Yaakov BenensonDepartment of Biosystems Science and Engineering, ETH Zurich, Basel, Switzerland.ORCID https://orcid.org/0000-0003-1880-6507

Funding

ETH Zurich Core Funding
6 · The paper itself

Abstract

Therapies targeting mutated rat sarcoma (RAS), the most frequently mutated oncogene in human cancers, could benefit millions of patients. Recently approved RAS inhibitors represent a breakthrough but are limited to a specific KRAS

Indexed as

Gene Regulatory NetworksGenes, SyntheticNeoplasmsras ProteinsAnimalsCell Line, TumorHumansMutationRatsSynthetic Biologyras Proteinsbiochemistrycancer biologycancer-targeted protein expressionchemical biologyhumanmulti-input logic circuitsRAS sensorsrat sarcoma oncogenesynthetic biologysynthetic gene circuits

Identifiers

PMID41733988
PMCPMC12931925

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.