Evidence map›Paper›PMID 30510853›Full record

ArticleOncoimmunology

Targeting phosphorylated p53 to elicit tumor-reactive T helper responses against head and neck squamous cell carcinoma.

Kenzo Ohara, Takayuki Ohkuri, Takumi Kumai, Toshihiro Nagato, Yui Nozaki, Kei Ishibashi, Akemi Kosaka, Marino Nagata, Shohei Harabuchi, Mizuho Ohara and 5 more

Open access · goldAbstract read
In one paragraph

Article in Oncoimmunology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.8field-weighted citation impact, top 23% 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

14 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
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  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Chemokine-Cytokine Networks in the Head and Neck Tumor Microenvironment.International journal of molecular sciences · 2021
    Review
  11. Article
  12. Review
  13. Article
  14. Article
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

15 authors at 2 institutions in 2 countries.

Kenzo OharaDepartment of Pathology, Asahikawa Medical University, Asahikawa, Japan.
Takayuki OhkuriDepartment of Pathology, Asahikawa Medical University, Asahikawa, Japan.
Takumi KumaiDepartment of Pathology, Asahikawa Medical University, Asahikawa, Japan.
Toshihiro NagatoDepartment of Pathology, Asahikawa Medical University, Asahikawa, Japan.
Yui NozakiDepartment of Pathology, Asahikawa Medical University, Asahikawa, Japan.
Kei IshibashiDepartment of Pathology, Asahikawa Medical University, Asahikawa, Japan.
Akemi KosakaDepartment of Pathology, Asahikawa Medical University, Asahikawa, Japan.
Marino NagataDepartment of Pathology, Asahikawa Medical University, Asahikawa, Japan.
Shohei HarabuchiDepartment of Pathology, Asahikawa Medical University, Asahikawa, Japan.
Mizuho OharaDepartment of Pathology, Asahikawa Medical University, Asahikawa, Japan.
Kensuke OikawaDepartment of Pathology, Asahikawa Medical University, Asahikawa, Japan.
Naoko AokiDepartment of Pathology, Asahikawa Medical University, Asahikawa, Japan.
Yasuaki HarabuchiDepartment of Otolaryngology-Head and Neck surgery, Asahikawa Medical University, Asahikawa, Japan.
Esteban CelisCancer Immunology, Inflammation and Tolerance Program, Augusta University, Georgia Cancer Center, Augusta, GA.
Hiroya KobayashiDepartment of Pathology, Asahikawa Medical University, Asahikawa, Japan.
Asahikawa Medical University · JPAugusta University Health · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The human T cell receptor is capable of distinguishing between normal and post-translationally modified peptides. Because aberrant phosphorylation of cellular proteins is a hallmark of malignant transformation, the expression of the phosphorylated epitope could be an ideal antigen to combat cancer without damaging normal tissues. p53 activates transcription factors to suppress tumors by upregulating growth arrest and apoptosis-related genes. In response to DNA damage, p53 is phosphorylated at multiple sites including Ser33 and Ser37. Here, we identified phosphorylated peptide epitopes from p53 that could elicit effective T helper responses. These epitope peptides, p53

Indexed as

CD4 T cellepitopehead and neck squamous cell carcinomaimmunotherapyp53phosphorylationpost-translational modification

Identifiers

PMID30510853
PMCPMC6259824
OpenAlexW2806834780

What OpenQuestion holds

Textmetadata
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.