Evidence map›Paper›PMID 31772160›Full record

ArticleNature communications2019

Targeting mutant p53-expressing tumours with a T cell receptor-like antibody specific for a wild-type antigen.

Lionel Low, Angeline Goh, Joanna Koh, Samantha Lim, Cheng-I Wang

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.2field-weighted citation impact, top 10% 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

36 citing papers in PubMed, 49 citations in OpenAlex.

  1. Revisiting tumor immunogenicity through the lens of mutant p53: Implications for cancer immunotherapy.Apoptosis : an international journal on programmed cell death · 2026
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  17. Heliyon · 2023
    Review
  18. Neoantigens: promising targets for cancer therapy.Signal transduction and targeted therapy · 2023
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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

5 authors at 2 institutions in 1 country.

Lionel LowSingapore Immunology Network, Agency for Science, Technology and Research, 8A Biomedical Grove, Singapore, 138648, Singapore.
Angeline GohSingapore Immunology Network, Agency for Science, Technology and Research, 8A Biomedical Grove, Singapore, 138648, Singapore.
Joanna KohSchool of Life Sciences and Chemical Technology, Ngee Ann Polytechnic, 535 Clementi Road, Singapore, 599489, Singapore.
Samantha LimSchool of Life Sciences and Chemical Technology, Ngee Ann Polytechnic, 535 Clementi Road, Singapore, 599489, Singapore.
Cheng-I WangSingapore Immunology Network, Agency for Science, Technology and Research, 8A Biomedical Grove, Singapore, 138648, Singapore. Wang_ChengI@immunol.a-star.edu.sg.
Agency for Science, Technology and Research · SGNgee Ann Polytechnic · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Accumulation of mutant p53 proteins is frequently found in a wide range of cancers. While conventional antibodies fail to target intracellular proteins, proteosomal degradation results in the presentation of p53-derived peptides on the tumour cell surface by class I molecules of the major histocompatibility complex (MHC). Elevated levels of such p53-derived peptide-MHCs on tumour cells potentially differentiate them from healthy tissues. Here, we report the engineering of an affinity-matured human antibody, P1C1TM, specific for the unmutated p53

Indexed as

AnimalsAntibodiesAntibody-Dependent Cell CytotoxicityAntineoplastic Agents, ImmunologicalCell Line, TumorCross ReactionsCytotoxicity, ImmunologicEpitopesHLA-A24 AntigenHumansMice, TransgenicMolecular Targeted TherapyMutationReceptors, Antigen, T-CellTumor Suppressor Protein p53Xenograft Model Antitumor AssaysAntibodiesAntineoplastic Agents, ImmunologicalEpitopesHLA-A24 AntigenReceptors, Antigen, T-CellTP53 protein, humanTumor Suppressor Protein p53

Identifiers

PMID31772160
PMCPMC6879612
OpenAlexW2990193820

What OpenQuestion 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 OpenQuestion graph.