Evidence map›Paper›PMID 30125801›Full record

ArticleTranslational oncology2018

Aminopeptidase N (CD13): Expression, Prognostic Impact, and Use as Therapeutic Target for Tissue Factor Induced Tumor Vascular Infarction in Soft Tissue Sarcoma.

Torsten Kessler, Ariane Baumeier, Caroline Brand, Michael Grau, Linus Angenendt, Saliha Harrach, Ursula Stalmann, Lars Henning Schmidt, Georg Gosheger, Jendrik Hardes and 9 more

Open access · goldAbstract read
In one paragraph

Article in Translational oncology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.5field-weighted citation impact, top 14% 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

16 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Biomaterials-Mediated Tumor Infarction Therapy.Frontiers in bioengineering and biotechnology · 2022
    Review
  7. Peptide-Based Drug Delivery Systems.Medicina (Kaunas, Lithuania) · 2021
    Review
  8. Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. 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

19 authors at 2 institutions in 1 country.

Torsten KesslerDepartment of Medicine A, Hematology, Oncology, University Hospital Muenster, Muenster, Germany. Electronic address: torstenkessler@uni-muenster.de.
Ariane BaumeierDepartment of Medicine A, Hematology, Oncology, University Hospital Muenster, Muenster, Germany.
Caroline BrandDepartment of Medicine A, Hematology, Oncology, University Hospital Muenster, Muenster, Germany.
Michael GrauDepartment of Medicine A, Hematology, Oncology, University Hospital Muenster, Muenster, Germany.
Linus AngenendtDepartment of Medicine A, Hematology, Oncology, University Hospital Muenster, Muenster, Germany.
Saliha HarrachDepartment of Medicine A, Hematology, Oncology, University Hospital Muenster, Muenster, Germany.
Ursula StalmannDepartment of Medicine A, Hematology, Oncology, University Hospital Muenster, Muenster, Germany.
Lars Henning SchmidtDepartment of Medicine A, Hematology, Oncology, University Hospital Muenster, Muenster, Germany.
Georg GoshegerDepartment of Orthopedics and Tumor-Orthopedics, University Hospital Muenster, Germany.
Jendrik HardesDepartment of Orthopedics and Tumor-Orthopedics, University Hospital Muenster, Germany.
Dimosthenis AndreouDepartment of Orthopedics and Tumor-Orthopedics, University Hospital Muenster, Germany.
Johannes DreischalückDepartment of Orthopedics and Trauma Surgery, Sankt Elisabeth Hospital Guetersloh, Guetersloh.
Georg LenzDepartment of Medicine A, Hematology, Oncology, University Hospital Muenster, Muenster, Germany; Translational Oncology, University Hospital Muenster, Muenster, Germany; Cluster of Excellence EXC 1003, Cells in Motion, Muenster, Germany.
Eva WardelmannGerhard-Domagk-Institute of Pathology, University of Muenster, Muenster, Germany.
Rolf M MestersDepartment of Medicine A, Hematology, Oncology, University Hospital Muenster, Muenster, Germany.
Christian SchwöppeDepartment of Medicine A, Hematology, Oncology, University Hospital Muenster, Muenster, Germany.
Wolfgang E BerdelDepartment of Medicine A, Hematology, Oncology, University Hospital Muenster, Muenster, Germany; Cluster of Excellence EXC 1003, Cells in Motion, Muenster, Germany. Electronic address: berdel@uni-muenster.de.
Wolfgang HartmannGerhard-Domagk-Institute of Pathology, University of Muenster, Muenster, Germany.
Christoph SchliemannDepartment of Medicine A, Hematology, Oncology, University Hospital Muenster, Muenster, Germany.
University Hospital Münster · DEAugenstern · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aminopeptidase N (CD13) is expressed on tumor vasculature and tumor cells. It represents a candidate for targeted therapy, e.g., by truncated tissue factor (tTF)-NGR, binding to CD13, and causing tumor vascular thrombosis. We analyzed CD13 expression by immunohistochemistry in 97 patients with STS who were treated by wide resection and uniform chemo-radio-chemotherapy. Using a semiquantitative score with four intensity levels, CD13 was expressed by tumor vasculature, or tumor cells, or both (composite value, intensity scores 1-3) in 93.9% of the STS. In 49.5% tumor cells, in 48.5% vascular/perivascular cells, and in 58.8%, composite value showed strong intensity score 3 staining. Leiomyosarcoma and synovial sarcoma showed low expression; fibrosarcoma and undifferentiated pleomorphic sarcoma showed high expression. We found a significant prognostic impact of CD13, as high expression in tumor cells or vascular/perivascular cells correlated with better relapse-free survival and overall survival. CD13 retained prognostic significance in multivariable analyses. Systemic tTF-NGR resulted in significant growth reduction of CD13-positive human HT1080 sarcoma cell line xenografts. Our results recommend further investigation of tTF-NGR in STS patients. CD13 might be a suitable predictive biomarker for patient selection.

Identifiers

PMID30125801
PMCPMC6113655
OpenAlexW2887709269

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.