Evidence map›Paper›PMID 28604655›Full record

ArticleLaboratory investigation; a journal of technical methods and pathology2017

Brain-derived neurotrophic factor/tropomyosin-related kinase B signaling pathway contributes to the aggressive behavior of lung squamous cell carcinoma.

Keigo Ozono, Yoshihiro Ohishi, Hideya Onishi, Katsuya Nakamura, Junichi Motoshita, Masato Kato, Ryoichi Nakanishi, Masafumi Nakamura, Yoshinao Oda

Open access · hybridAbstract readComparative Study
PubMed Publisher
In one paragraph

Article in Laboratory investigation; a journal of technical methods and pathology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.6field-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

17 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Review
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  7. Article
  8. Epigenetics in psoriasis: perspective of DNA methylation.Molecular genetics and genomics : MGG · 2021
    Review
  9. Novel Emerging Molecular Targets in Non-Small Cell Lung Cancer.International journal of molecular sciences · 2021
    Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. CD271 is a negative prognostic factor and essential for cell proliferation in lung squamous cell carcinoma.Laboratory investigation; a journal of technical methods and pathology · 2019
    Article
  15. Article
  16. Article
  17. New targets bring hope in squamous cell lung cancer: neurotrophic tyrosine kinase gene fusions.Laboratory investigation; a journal of technical methods and pathology · 2017
    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

9 authors at 4 institutions in 1 country.

Keigo OzonoDepartment of Anatomic Pathology, Kyushu University, Fukuoka, Japan.
Yoshihiro OhishiDepartment of Anatomic Pathology, Kyushu University, Fukuoka, Japan.
Hideya OnishiDepartment of Cancer Therapy and Research, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Katsuya NakamuraDepartment of Cancer Therapy and Research, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Junichi MotoshitaDepartment of Diagnostic Pathology, Hamanomachi Hospital, Fukuoka, Japan.
Masato KatoDepartment of Surgery, Hiramatsu Hospital, Saga, Japan.
Ryoichi NakanishiDepartment of Oncology, Immunology and Surgery, Graduate School of Medical Sciences and Medical School, Nagoya City University, Nagoya, Japan.
Masafumi NakamuraDepartment of Surgery and Oncology, Kyushu University, Fukuoka, Japan.
Yoshinao OdaDepartment of Anatomic Pathology, Kyushu University, Fukuoka, Japan.
Kyushu University · JPHamanomachi Hospital · JPKyushu Hospital · JPNagoya City University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The tropomyosin-related kinase (Trk) family consists of TrkA, TrkB, and TrkC, which play essential roles in tumor progression and/or suppression in various cancers. Little is known about the biological significance of the Trk family in human lung squamous cell carcinoma (SCC). Here we investigated the clinical significance of the protein expression of Trk family members in samples from 99 SCC patients, and we explored the relationship between invasion/proliferation activities and Trk expression using lung SCC cell lines to clarify the biological significance of the Trk family in lung SCC. Immunohistochemical high expression of TrkB was significantly correlated with vascular invasion (P=0.004), lymph node metastasis (P<0.001), and advanced stage (P=0.0015). The overall survival of the patients with TrkB-high expression was significantly shorter than those with TrkB-low expression (P=0.0110). TrkA/TrkC expressions were not predictors of poor prognosis. An in vitro assay demonstrated that the inhibition of brain-derived neurotrophic factor (BDNF) (a TrkB ligand) and TrkB by K252a (a Trk inhibitor) or siRNA (BDNF-siRNA, TrkB-siRNA) suppressed the invasion, migration, and proliferative activities of lung SCC cells. The administration of recombinant human BDNF (rhBDNF) enhanced the invasion, migration, and proliferation activities, which were abrogated by K252a. TrkB-siRNA transfection increased the protein expression of E-cadherin and decreased vimentin expressions in lung SCC cells. Matrix metalloproteinase-2 (MMP-2)-mediated gelatin degradations were decreased in lung SCC cells transfected with TrkB-siRNA. Thus, TrkB-high expression is an indicator of poor prognosis in lung SCC, probably due to invasion/proliferation activities promoted by the BDNF/TrkB signaling pathway, which could become a therapeutic target for lung SCC.

Indexed as

Signal TransductionBrain-Derived Neurotrophic FactorCarcinoma, Squamous CellCell Line, TumorCell ProliferationFemaleHumansLungLung NeoplasmsMaleMembrane GlycoproteinsMiddle AgedNeoplasm GradingNeoplasm InvasivenessNeoplasm ProteinsNeoplasm StagingBDNF protein, humanBrain-Derived Neurotrophic FactorMembrane GlycoproteinsNeoplasm ProteinsNTRK1 protein, humanReceptor, trkAReceptor, trkBReceptor, trkCRecombinant Proteinstropomyosin-related kinase-B, human

Identifiers

PMID28604655
OpenAlexW2623953495

What OpenQuestion holds

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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.