Evidence map›Paper›PMID 27888795›Full record

ArticleOncotarget2017

Targeting tachykinin receptors in neuroblastoma.

Anton G Henssen, Andrea Odersky, Annabell Szymansky, Marleen Seiler, Kristina Althoff, Anneleen Beckers, Frank Speleman, Simon Schäfers, Katleen De Preter, Kathy Astrahanseff and 5 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 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
2.2field-weighted citation impact, top 12% 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, 29 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Peptidergic Systems and Neuroblastoma.International journal of molecular sciences · 2025
    Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Review
  17. 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

15 authors at 5 institutions in 3 countries.

Anton G HenssenMolecular Pharmacology Program, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, USA.
Andrea OderskyDepartment of Pediatric Oncology and Hematology, University Children's Hospital Essen, Germany.
Annabell SzymanskyDepartment of Pediatric Oncology/Hematology, Charité- Universitätsmedizin Berlin, Germany.
Marleen SeilerSphingotec GmbH, Hennigsdorf, Germany.
Kristina AlthoffDepartment of Pediatric Oncology and Hematology, University Children's Hospital Essen, Germany.
Anneleen BeckersCenter of Medical Genetics Ghent (CMGG), Ghent University Hospital, Belgium.
Frank SpelemanCenter of Medical Genetics Ghent (CMGG), Ghent University Hospital, Belgium.
Simon SchäfersDepartment of Pediatric Oncology and Hematology, University Children's Hospital Essen, Germany.
Katleen De PreterCenter of Medical Genetics Ghent (CMGG), Ghent University Hospital, Belgium.
Kathy AstrahanseffDepartment of Pediatric Oncology/Hematology, Charité- Universitätsmedizin Berlin, Germany.
Joachim StruckSphingotec GmbH, Hennigsdorf, Germany.
Alexander SchrammDepartment of Pediatric Oncology and Hematology, University Children's Hospital Essen, Germany.
Angelika EggertDepartment of Pediatric Oncology/Hematology, Charité- Universitätsmedizin Berlin, Germany.
Andreas BergmannSphingotec GmbH, Hennigsdorf, Germany.
Johannes H SchulteDepartment of Pediatric Oncology/Hematology, Charité- Universitätsmedizin Berlin, Germany.
Essen University Hospital · DECharité - Universitätsmedizin Berlin · DEGhent University Hospital · BEGerman Cancer Society · DEMemorial Sloan Kettering Cancer Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neuroblastoma is the most common extracranial tumor in children. Despite aggressive multimodal treatment, high-risk neuroblastoma remains a clinical challenge with survival rates below 50%. Adding targeted drugs to first-line therapy regimens is a promising approach to improve survival in these patients. TACR1 activation by substance P has been reported to be mitogenic in cancer cell lines. Tachykinin receptor (TACR1) antagonists are approved for clinical use as an antiemetic remedy since 2003. Tachykinin receptor inhibition has recently been shown to effectively reduce growth of several tumor types. Here, we report that neuroblastoma cell lines express TACR1, and that targeting TACR1 activity significantly reduced cell viability and induced apoptosis in neuroblastoma cell lines. Gene expression profiling revealed that TACR1 inhibition repressed E2F2 and induced TP53 signaling. Treating mice harboring established neuroblastoma xenograft tumors with Aprepitant also significantly reduced tumor burden. Thus, we provide evidence that the targeted inhibition of tachykinin receptor signaling shows therapeutic efficacy in preclinical models for high-risk neuroblastoma.

Indexed as

AnimalsAntineoplastic AgentsApoptosisAprepitantCell Line, TumorCell ProliferationCell SurvivalDrug Evaluation, PreclinicalE2F2 Transcription FactorEnzyme-Linked Immunosorbent AssayFemaleFlow CytometryGene Expression ProfilingHumansMiceMice, NudeAntineoplastic AgentsAprepitantE2F2 protein, humanE2F2 Transcription FactorfosaprepitantMorpholinesNeurokinin-1 Receptor AntagonistsProdrugsReceptors, Neurokinin-1TP53 protein, humanTumor Suppressor Protein p53aprepitantfosaprepitantneuroblastomaNK1Rtargeted therapy

Identifiers

PMID27888795
PMCPMC5352132
OpenAlexW2552323466

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.