Evidence map›Paper›PMID 35205828›Full record

ArticleCancers2022

NOTCH1 Intracellular Domain and the Tumor Microenvironment as Prognostic Markers in HNSCC.

Benedikt Schmidl, Michael Siegl, Melanie Boxberg, Fabian Stögbauer, Daniel Jira, Christof Winter, Leonhard Stark, Anja Pickhard, Barbara Wollenberg, Markus Wirth

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.0field-weighted citation impact, top 28% 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

9 citing papers in PubMed, 11 citations in OpenAlex.

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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 1 institution in 1 country.

Benedikt SchmidlDepartment of Otolaryngology Head and Neck Surgery, Technical University Munich, 81675 Munich, Germany.
Michael SieglDepartment of Otolaryngology Head and Neck Surgery, Technical University Munich, 81675 Munich, Germany.
Melanie BoxbergInstitute of Pathology, Technical University Munich, 81675 Munich, Germany.
Fabian StögbauerInstitute of Pathology, Technical University Munich, 81675 Munich, Germany.
Daniel JiraDepartment of Otolaryngology Head and Neck Surgery, Technical University Munich, 81675 Munich, Germany.ORCID 0000-0001-5822-892X
Christof WinterInstitute of Clinical Chemistry and Pathobiochemistry, Technical University Munich, 81675 Munich, Germany.ORCID 0000-0002-0253-9056
Leonhard StarkDepartment of Otolaryngology Head and Neck Surgery, Technical University Munich, 81675 Munich, Germany.
Anja PickhardDepartment of Otolaryngology Head and Neck Surgery, Technical University Munich, 81675 Munich, Germany.
Barbara WollenbergDepartment of Otolaryngology Head and Neck Surgery, Technical University Munich, 81675 Munich, Germany.ORCID 0000-0002-3062-459X
Markus WirthDepartment of Otolaryngology Head and Neck Surgery, Technical University Munich, 81675 Munich, Germany.
Technical University of Munich · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

(1) Background: NOTCH1 is the second most common mutated gene in whole-exome sequencing of HNSCC. The aim of this project was to gain further insight into the relevance of NOTCH1 in HNSCC, potentially establishing NOTCH1 as a prognostic marker or therapeutic target; (2) Methods: NOTCH1 was silenced via RNA interference in six HNSCC cell lines and the impact was evaluated in migration and proliferation assays. Subsequently, the protein expression of NOTCH1 intracellular domain (NICD) and NOTCH1 mRNA expression were examined in 70 oropharyngeal squamous cell cancer tissue samples. Lastly, the NICD expression was compared with the local infiltration of lymphocytes, measured with the immunoscore; (3) Results: Knockdown of NOTCH1 decreased migration and proliferation. A high NICD expression was associated with lower OS. A high immunoscore resulted in significantly better OS. NICD expression was independent of the immunoscore and as a whole differentiated three distinct prognostic groups; (4) Conclusions: These data suggest that NOTCH1 is involved in migration and proliferation of HNSCC cell lines. In vivo, NICD expression was associated with overall survival and could, therefore, be used as a prognostic marker. NICD expression differs from NOTCH1 mRNA levels, potentially explaining the previously suggested bimodal role as an oncogene and tumor suppressor in HNSCC.

Indexed as

HNSCCHPVimmune systemimmunoscoreNICDNOTCH1OPSCC

Identifiers

PMID35205828
PMCPMC8870336
OpenAlexW4213265763

What OpenQuestion holds

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Registered trials

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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.