Evidence map›Paper›PMID 37894290›Full record

ArticleCancers2023

Combined Biomarker System Predicts Prognosis in Patients with Metastatic Oral Squamous Cell Carcinoma.

Tatjana Khromov, Lucas Fischer, Andreas Leha, Felix Bremmer, Andreas Fischer, Henning Schliephake, Michal Amit Rahat, Phillipp Brockmeyer

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

6 citing papers in PubMed, 5 citations in OpenAlex.

  1. Beyond the gap: moonlighting functions of connexins in cancer.Cell communication and signaling : CCS · 2026
    Review
  2. Article
  3. CD147/Basigin: From Integrative Molecular Hub to Translational Therapeutic Target.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  4. Article
  5. Article
  6. Review
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

8 authors at 2 institutions in 2 countries.

Tatjana KhromovDepartment of Clinical Chemistry, University Medical Center Goettingen, 37075 Goettingen, Germany.ORCID 0000-0002-5340-9593
Lucas FischerDepartment of Urology, University Medical Center Goettingen, 37075 Goettingen, Germany.
Andreas LehaDepartment of Medical Statistics, University Medical Center Goettingen, 37075 Goettingen, Germany.ORCID 0000-0002-8072-1988
Felix BremmerInstitute of Pathology, University Medical Center Goettingen, 37075 Goettingen, Germany.
Andreas FischerDepartment of Clinical Chemistry, University Medical Center Goettingen, 37075 Goettingen, Germany.ORCID 0000-0002-4889-0909
Henning SchliephakeDepartment of Oral and Maxillofacial Surgery, University Medical Center Goettingen, 37075 Goettingen, Germany.ORCID 0000-0002-2008-7188
Michal Amit RahatImmunotherapy Laboratory, Carmel Medical Center, Haifa 3436212, Israel.ORCID 0000-0002-1881-1173
Phillipp BrockmeyerDepartment of Oral and Maxillofacial Surgery, University Medical Center Goettingen, 37075 Goettingen, Germany.ORCID 0000-0003-3694-2828
University of Göttingen · DETechnion – Israel Institute of Technology · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMetastatic oral squamous cell carcinoma (OSCC) is associated with poor patient prognosis. Metastasis is a complex process involving various proteins, tumor cell alterations, including changes attributable to the epithelial-to-mesenchymal transition (EMT) process, and interactions with the tumor microenvironment (TME). In this study, we investigate a combined protein marker system consisting of connexin 43 (Cx43), EMMPRIN (CD147), E-cadherin, and vimentin, with a focus on their roles in the invasive metastatic progression of OSCC and their potential utility in predicting prognosis.

methodsWe conducted an immunohistochemical analysis to assess the protein expression profiles of Cx43, EMMPRIN, E-cadherin, and vimentin using tissue samples obtained from 24 OSCC patients. The metastatic process was mapped through different regions of interest (ROIs), including adjacent healthy oral mucosa (OM), center of primary OSCC, invasive front (IF), and local cervical lymph node metastases (LNM). The primary clinical endpoints were disease-free survival (DFS) and overall survival (OS).

resultsSubstantial changes in the expression profiles of the different marker proteins were observed among the different ROIs, with all

conclusionsThe combined marker system exhibited a significant ability to predict patient prognosis. An increase in EMMPRIN expression toward the IF showed the strongest effect and could be an interesting new antimetastatic therapy approach.

Indexed as

connexin 43disease-free survivalE-cadherinEMMPRINepithelial-to-mesenchymal transitionmetastasisoral squamous cell carcinomaoverall survivalprognosisvimentin

Identifiers

PMID37894290
PMCPMC10605069
OpenAlexW4387494742

What OpenQuestion holds

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LicenceCC BY
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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.