Evidence map›Paper›PMID 14762710›Full record

ArticleJournal of cancer research and clinical oncology2004

Tyrosine kinase receptor expression in thymomas.

John D Henley, Oscar W Cummings, Patrick J Loehrer

Open access · greenAbstract read
In one paragraph

Article in Journal of cancer research and clinical oncology, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 2 pooled it
4.0field-weighted citation impact, top 7% 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

24 citing papers in PubMed, 2 syntheses or guidelines pooled it, 85 citations in OpenAlex.

  1. Pooled it
  2. [Policies and reporting guidelines for small biopsy specimens of mediastinal masses].Zhongguo fei ai za zhi = Chinese journal of lung cancer · 2014
    Guideline
  3. Imatinib mesylate in patients with WHO B3 thymomas and thymic carcinomas.Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer · 2009
    Trial
  4. Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Thymic epithelial tumours: from basic principles to individualised treatment strategies.European respiratory review : an official journal of the European Respiratory Society · 2013
    Review
  14. Article
  15. Article
  16. Thymic malignancies: from clinical management to targeted therapies.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2011
    Review
  17. Targeted therapy for advanced thymic tumors.Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer · 2010
    Review
  18. Expression and mutational status of c-kit in thymic epithelial tumors.Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer · 2010
    Article
  19. Article
  20. Comprehensive genomic analysis reveals clinically relevant molecular distinctions between thymic carcinomas and thymomas.Clinical cancer research : an official journal of the American Association for Cancer Research · 2009
    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

3 authors at 2 institutions in 1 country.

John D HenleyDepartment of Pathology, Indiana University School of Medicine, Clarian Health Partners, 550 North University Blvd, Rm 3465, Indianapolis 46202, USA. jhenley@iupui.edu
Oscar W Cummings
Patrick J Loehrer
Indiana University – Purdue University Indianapolis · USIndiana University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposePromising new therapies for neoplasia include tyrosine kinase receptor antagonists. Tyrosine kinase oncogenes present an appealing anti-tumor drug target since they play an integral role in a variety of cellular responses including cell proliferation and differentiation. We previously demonstrated a high rate of epidermal growth factor receptor (EGFR) expression in advanced-stage thymic epithelial tumors. More recently, we have examined c-KIT (CD117) expression in a similar series of tumors.

methodsTumor from 35 patients seen at our institution for treatment of advanced-stage thymoma was available. Twenty thymomas and 15 thymic carcinomas were assessed for c-KIT expression. Tissue sections of tumor were stained immunohistochemically with anti-c-KIT (Oncogene). Either cytoplasmic or membrane staining was considered positive. Appropriate controls were performed. Positive staining for c-KIT was present in 12 tumors (11 thymic carcinomas and 1 thymoma).

resultsIn distinction to EGFR, c-KIT is expressed more commonly in thymic carcinomas (73% of carcinomas) than in thymoma (5% of thymomas).

conclusionsAn EGFR negative/c-KIT positive staining pattern is typical of thymic carcinoma, whereas thymomas are generally EGFR positive/c-KIT negative. Possible therapeutic implications of these observations remain to be determined.

Indexed as

CarcinomaGene Expression Regulation, NeoplasticHumansImmunohistochemistryProto-Oncogene Proteins c-kitReceptor Protein-Tyrosine KinasesThymomaThymus NeoplasmsProto-Oncogene Proteins c-kitReceptor Protein-Tyrosine Kinases

Identifiers

PMID14762710
PMCPMC12161833
OpenAlexW2056129513

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.