Evidence map›Paper›PMID 16877360›Full record

ArticleThe American journal of pathology2006

Relaxin enhances the oncogenic potential of human thyroid carcinoma cells.

Sabine Hombach-Klonisch, Joanna Bialek, Bogusz Trojanowicz, Ekkehard Weber, Hans-Jürgen Holzhausen, Josh D Silvertown, Alastair J Summerlee, Henning Dralle, Cuong Hoang-Vu, Thomas Klonisch

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
4.8field-weighted citation impact, top 6% 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

29 citing papers in PubMed, 75 citations in OpenAlex.

  1. Article
  2. Role of Relaxin Signaling in Cancer: A Review.Biochemical pharmacology · 2024
    Review
  3. Article
  4. Review
  5. Article
  6. The dual and multifaceted role of relaxin-2 in cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2023
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. BRAFJournal of cancer research and clinical oncology · 2021
    Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. Relaxin-2 expression in temporal bone carcinoma.European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery · 2015
    Article
  20. 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

10 authors at 5 institutions in 4 countries.

Sabine Hombach-KlonischDepartment of Human Anatomy and Cell Science, Faculty of Medicine, University of Manitoba, 130 Basic Medical Sciences, 730 William Ave., Winnipeg, MB, R3E 0W3, Canada. klonisch@cc.umanitoba.ca
Joanna Bialek
Bogusz Trojanowicz
Ekkehard Weber
Hans-Jürgen Holzhausen
Josh D Silvertown
Alastair J Summerlee
Henning Dralle
Cuong Hoang-Vu
Thomas Klonisch
Physiological Society · GBMartin Luther University Halle-Wittenberg · DEUniversity of Manitoba · CAOntario Institute for Cancer Research · CAUniversity of Guelph · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The role of members of the insulin-like superfamily in human thyroid carcinoma is primarily unknown. Here we demonstrate the presence of RLN2 relaxin and relaxin receptor LGR7 in human papillary, follicular, and undifferentiated anaplastic thyroid carcinoma suggesting a specific involvement of relaxin-LGR7 signaling in thyroid carcinoma. Stable transfectants of the LGR7-positive human follicular thyroid carcinoma cell lines FTC-133 and FTC-238 that secrete bioactive proRLN2 revealed this hormone to act as a multifunctional endocrine factor in thyroid carcinoma cells. Although RLN2 did not act as a mitogen, it acted as an autocrine/paracrine factor and significantly increased anchorage-independent growth and thyroid carcinoma cell motility and invasiveness through elastin matrices. Suppression of LGR7 expression by LGR7-siRNA abolished the RLN2-mediated accelerated tumor cell motility. The increased elastinolytic activity correlated with enhanced production and secretion of the lysosomal proteinases cathepsin-D (cath-D) and cath-L forms hereby identified as new RLN2 target molecules in human neoplastic thyrocytes. We found the intracellular distribution of procath-L specifically altered in RLN2 transfectants, providing first evidence for selective actions of relaxin on the powerful elastinolytic cath-L production, storage, and secretion in thyroid carcinoma cells. Thus, relaxin enhances the oncogenic potential and acts as novel endocrine modulator of invasiveness in human thyroid carcinoma cells.

Indexed as

AdolescentAdultAgedCarcinomaCathepsinsCell Line, TumorCell MovementChildElastinFemaleGene Expression Regulation, NeoplasticHumansMaleMembrane ProteinsMiddle AgedNeoplasm InvasivenessCathepsinsElastinMembrane ProteinsReceptors, G-Protein-CoupledReceptors, PeptideRelaxinRLN2 protein, humanRNA, MessengerRXFP1 protein, human

Identifiers

PMID16877360
PMCPMC1698779
OpenAlexW1964200501

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.