Evidence map›Paper›PMID 27392476›Full record

ReviewMolecular diagnosis & therapy2016

Follicle-Stimulating Hormone Receptor (FSHR): A Promising Tool in Oncology?

Konstantinos Papadimitriou, Panteleimon Kountourakis, Anastasia E Kottorou, Anna G Antonacopoulou, Christian Rolfo, Marc Peeters, Haralabos P Kalofonos

Abstract readReview
PubMed Publisher
In one paragraph

Review in Molecular diagnosis & therapy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
5.7field-weighted citation impact, top 4% 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

23 citing papers in PubMed, 45 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Modeling Host-Pathogen Interactions inInternational journal of molecular sciences · 2024
    Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Recent Applications of Retro-Inverso Peptides.International journal of molecular sciences · 2021
    Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Review
  16. Review
  17. Review
  18. FSH receptor binding inhibitor up-regulates ARID1A and PTEN genes associated with ovarian cancers in mice.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2019
    Article
  19. Article
  20. 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

7 authors at 2 institutions in 2 countries.

Konstantinos PapadimitriouDepartment of Medical Oncology, University Hospital of Antwerp, 10 Wilrijksraat, 2650, Edegem, Belgium. padimko@gmail.com.
Panteleimon KountourakisDepartment of Medical Oncology, B.O.C. Oncology Centre, Nicosia, Cyprus.
Anastasia E KottorouDepartment of Medical Oncology, University Hospital of Patra, Rio, Greece.
Anna G AntonacopoulouDepartment of Medical Oncology, University Hospital of Patra, Rio, Greece.
Christian RolfoDepartment of Medical Oncology, University Hospital of Antwerp, 10 Wilrijksraat, 2650, Edegem, Belgium.
Marc PeetersDepartment of Medical Oncology, University Hospital of Antwerp, 10 Wilrijksraat, 2650, Edegem, Belgium.
Haralabos P KalofonosDepartment of Medical Oncology, University Hospital of Patra, Rio, Greece.
Antwerp University Hospital · BEGeneral University Hospital of Patras · GR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The cellular pathway of follicle-stimulating hormone (FSH) and its receptor (FSHR) is typically involved in reproduction in mammals. In humans, the FSHR is normally found in cells of the testis and the ovary, while it is scarcely expressed in other normal tissues. The expression of FSH/FSHR is studied in prostate, thyroid, and ovarian cancer tissues. Recently, the expression of FSHR was uniformly documented in malignant vascular endothelial cells from different tumor types, while in normal or inflammatory tissues its expression was scarce, suggesting a potential role of a pan-receptor in cancer. Subsequent studies have attempted to verify this unique specificity of this molecule and further define its features in malignant microenvironments but have had conflicting results, mostly because of differing techniques and immaturity of antibodies. Still, the lack of FSHR expression in most non-cancerous cells, in contrast to its specific correlation with the malignant tissue microenvironment, implies a potential role as both a diagnostic and a therapeutic tool. FSHR might also have a very specific role in malignancies, such as angiogenic and/or growth factor malignancies, but this is yet to be validated. Moreover, the expression of FSHR in endothelial malignant cells could have a predictive impact on disease progression, especially in relation to therapies targeting the tumor vasculature. In this review we look deep into the physiology of the FSH/FSHR pathway and evaluate the potential of FSHR as a predictive and prognostic tool in oncology.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsCell Line, TumorDisease ProgressionFemaleGenetic TherapyHumansMaleMutationNeoplasmsOvarian NeoplasmsPolymorphism, Single NucleotidePrognosisProstatic NeoplasmsReceptors, FSHThyroid NeoplasmsReceptors, FSH

Identifiers

PMID27392476
OpenAlexW2471488011

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.