Evidence map›Paper›PMID 26538233›Full record

ArticleScientific reports2015

Targeting HER-3 to elicit antitumor helper T cells against head and neck squamous cell carcinoma.

Takumi Kumai, Takayuki Ohkuri, Toshihiro Nagato, Yoshinari Matsuda, Kensuke Oikawa, Naoko Aoki, Shoji Kimura, Esteban Celis, Yasuaki Harabuchi, Hiroya Kobayashi

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.0field-weighted citation impact, top 21% 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

19 citing papers in PubMed, 29 citations in OpenAlex.

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  11. Targeting the ERβ/HER Oncogenic Network inInternational journal of molecular sciences · 2021
    Article
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  13. Thirty Years of HER3: From Basic Biology to Therapeutic Interventions.Clinical cancer research : an official journal of the American Association for Cancer Research · 2021
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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

10 authors at 2 institutions in 2 countries.

Takumi KumaiDepartment of Pathology, Asahikawa Medical University, Asahikawa, Japan.
Takayuki OhkuriDepartment of Pathology, Asahikawa Medical University, Asahikawa, Japan.
Toshihiro NagatoDepartment of Otolaryngology, Head and Neck Surgery, Asahikawa Medical University, Asahikawa, Japan.
Yoshinari MatsudaDepartment 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.
Shoji KimuraDepartment of Pathology, Asahikawa Medical University, Asahikawa, Japan.
Esteban CelisCancer Immunology, Inflammation and Tolerance Program, Georgia Regents University Cancer Center, Augusta, GA.
Yasuaki HarabuchiDepartment of Otolaryngology, Head and Neck Surgery, Asahikawa Medical University, Asahikawa, Japan.
Hiroya KobayashiDepartment of Pathology, Asahikawa Medical University, Asahikawa, Japan.
Asahikawa Medical University · JPGeorgia Regents Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

HER-3 expression has been reported to act as an important oncoprotein in head and neck squamous cell carcinoma. This protein is known to control tumor proliferation and acquisition of resistance by tumor cells towards EGFR inhibitors, therefore, development of a HER-3-targeted therapy is desirable. In this study, we found that HER-3 expression on tumor cells was increased after EGFR inhibition. To establish a novel therapeutic approach for HER-3-positive head and neck carcinoma, we identified a HER-3 helper epitope that could elicit effective helper T cell responses to the naturally processed HER-3-derived epitope presented in a HER-3 expressing tumors. This epitope induced potent cytolytic activity of CD4 T cells against such tumor cells. Moreover, pan HER-family tyrosine kinase inhibitor augmented the responses of HER-3-reactive CD4 T cells via upregulation of HLA-DR protein on the surface of tumor cells. Our results supports the validity of CD4 T cell-dependent HER-3-targeted therapy combined with a broad inhibitor of HER-family.

Indexed as

AnimalsCarcinoma, Squamous CellCD4-Positive T-LymphocytesCell LineCell Line, TumorEpitopes, T-LymphocyteErbB ReceptorsHead and Neck NeoplasmsHLA-DR AntigensHumansJurkat CellsLymphocyte ActivationMiceProtein Kinase InhibitorsReceptor, ErbB-3T-Lymphocytes, Helper-InducerEpitopes, T-LymphocyteErbB ReceptorsHLA-DR AntigensProtein Kinase InhibitorsReceptor, ErbB-3

Identifiers

PMID26538233
PMCPMC4633732
OpenAlexW2256596092

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.