Evidence map›Paper›PMID 34045312›Full record

ArticleMolecular cancer research : MCR2021

p53 Frameshift Mutations Couple Loss-of-Function with Unique Neomorphic Activities.

David R Tong, Wen Zhou, Chen Katz, Kausik Regunath, Divya Venkatesh, Chinyere Ihuegbu, James J Manfredi, Oleg Laptenko, Carol Prives

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in Molecular cancer research : MCR, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.2field-weighted citation impact, top 19% 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

11 citing papers in PubMed, 17 citations in OpenAlex.

  1. Impact of differentTranslational lung cancer research · 2026
    Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Involvement ofFrontiers in oncology · 2025
    Review
  7. Article
  8. The spectrum of TP53 mutations in Rwandan patients with gastric cancer.Genes and environment : the official journal of the Japanese Environmental Mutagen Society · 2024
    Article
  9. Article
  10. Article
  11. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

David R TongDepartment of Biological Sciences, Columbia University, New York, New York.
Wen ZhouDepartment of Biological Sciences, Columbia University, New York, New York.ORCID 0000-0002-5496-5815
Chen KatzDepartment of Biological Sciences, Columbia University, New York, New York.
Kausik RegunathDepartment of Biological Sciences, Columbia University, New York, New York.ORCID 0000-0002-2437-3851
Divya VenkateshDepartment of Biological Sciences, Columbia University, New York, New York.
Chinyere IhuegbuDepartment of Biological Sciences, Columbia University, New York, New York.
James J ManfrediDepartment of Oncological Sciences, Tisch Cancer Institute, Graduate School of Biomedical Sciences, Icahn School of Medicine at Mount Sinai, New York, New York.ORCID 0000-0003-2234-9097
Oleg LaptenkoDepartment of Biological Sciences, Columbia University, New York, New York. clp3@columbia.edu olaptenkooa@gmail.com.
Carol PrivesDepartment of Biological Sciences, Columbia University, New York, New York. clp3@columbia.edu olaptenkooa@gmail.com.
Columbia University · USTisch Hospital · US

Funding

Functions and Activities of p53 and Mdm2 in Normal and Cancer CellsR35CA220526 · NCI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI PRIVES, CAROL · 2018 to 2024
$6.0M
Role of the p53 C-terminal domain in tissue homeostasis, tumor suppression, and oncogenesisR01CA196234 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI MANFREDI, JAMES J, PRIVES, CAROL · 2016 to 2020
$3.0M
Cell lineage determinants of p53-driven fate outcomes in vivoR01CA257548 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI MANFREDI, JAMES J, PRIVES, CAROL · 2021 to 2025
$3.0M
NCI NIH HHS R01 CA196234NCI NIH HHS R01 CA257548NCI NIH HHS R35 CA220526
6 · The paper itself

Abstract

p53 mutations that result in loss of transcriptional activity are commonly found in numerous types of cancer. While the majority of these are missense mutations that map within the central DNA-binding domain, truncations and/or frameshift mutations can also occur due to various nucleotide substitutions, insertions, or deletions. These changes result in mRNAs containing premature stop codons that are translated into a diverse group of C-terminally truncated proteins. Here we characterized three p53 frameshift mutant proteins expressed from the endogenous

Indexed as

Frameshift MutationGene Expression Regulation, NeoplasticLoss of Function MutationApoptosisBiomarkers, TumorBone NeoplasmsCell CycleCell MovementCell ProliferationColorectal NeoplasmsHumansOsteosarcomaTumor Cells, CulturedTumor Suppressor Protein p53Biomarkers, TumorTP53 protein, humanTumor Suppressor Protein p53

Identifiers

PMID34045312
PMCPMC8419077
OpenAlexW3164832704

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.