Evidence map›Paper›PMID 41918356›Full record

ArticleCancer discovery2026

The Moving Target: Cis-Mutation-Driven Resistance to p53-Y220C Reactivator.

Yanqing Liu, Wei Gu

Abstract readComment
PubMed Publisher
In one paragraph

Article in Cancer discovery, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors.

Yanqing LiuInstitute for Cancer Genetics, Herbert Irving Comprehensive Cancer Center, Columbia University, New York, New York.ORCID 0000-0002-3520-1887
Wei GuInstitute for Cancer Genetics, Herbert Irving Comprehensive Cancer Center, Columbia University, New York, New York.ORCID 0000-0002-1480-2368

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The study by Fece de la Cruz, Varkaris, and colleagues uncovered a critical mechanism underlying resistance to the p53-Y220C reactivator rezatapopt in the PYNNACLE clinical trial. Specifically, rezatapopt treatment was shown to select for secondary mutations in the TP53 gene on the Y220C-mutant background, thereby abrogating its therapeutic efficacy. See related article by Fece de la Cruz et al., p. 677.

Indexed as

Antineoplastic AgentsDrug Resistance, NeoplasmNeoplasmsTumor Suppressor Protein p53Clinical Trials as TopicHumansMutation, MissenseAntineoplastic AgentsTumor Suppressor Protein p53

Identifiers

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.