Evidence map›Paper›PMID 27443788›Full record

ReviewBritish journal of pharmacology2017

Structural commonality of C1q TNF-related proteins and their potential to activate relaxin/insulin-like family peptide receptor 1 signalling pathways in cancer cells.

Thomas Klonisch, Aleksandra Glogowska, Thatchawan Thanasupawat, Maxwell Burg, Jerry Krcek, Marshall Pitz, Appalaraju Jaggupilli, Prashen Chelikani, G William Wong, Sabine Hombach-Klonisch

Abstract readReview
In one paragraph

Review in British journal of pharmacology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
–field-weighted citation impact
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

21 citing papers in PubMed.

  1. Description of a Large Family with Periodic Fever Carrying a Variant inInternational journal of molecular sciences · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. C1q and central nervous system disorders.Frontiers in immunology · 2023
    Review
  9. Review
  10. Article
  11. Review
  12. Review
  13. Complement's favourite organelle-Mitochondria?British journal of pharmacology · 2021
    Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  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

10 authors.

Thomas KlonischDepartment of Human Anatomy and Cell Science, University of Manitoba, Winnipeg, MB, Canada.
Aleksandra GlogowskaDepartment of Human Anatomy and Cell Science, University of Manitoba, Winnipeg, MB, Canada.
Thatchawan ThanasupawatDepartment of Human Anatomy and Cell Science, University of Manitoba, Winnipeg, MB, Canada.
Maxwell BurgDepartment of Human Anatomy and Cell Science, University of Manitoba, Winnipeg, MB, Canada.
Jerry KrcekDepartment of Human Anatomy and Cell Science, University of Manitoba, Winnipeg, MB, Canada.
Marshall PitzDepartment of Internal Medicine, University of Manitoba, Winnipeg, MB, Canada.
Appalaraju JaggupilliDepartment of Oral Biology, University of Manitoba, Winnipeg, MB, Canada.
Prashen ChelikaniDepartment of Oral Biology, University of Manitoba, Winnipeg, MB, Canada.
G William WongDepartment of Physiology and Center for Metabolism and Obesity Research, Johns Hopkins School of Medicine, Baltimore, MD, USA.
Sabine Hombach-KlonischDepartment of Human Anatomy and Cell Science, University of Manitoba, Winnipeg, MB, Canada.

Funding

CTRP and Metabolic ControlR01DK084171 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI Guang William Wong · 2010 to 2026
$8.0M
NIDDK NIH HHS R01 DK084171
6 · The paper itself

Abstract

We established the role of the GPCR relaxin/insulin-like family peptide receptor 1 (RXFP1 receptor) as a novel active receptor in human glioblastoma (GB), a fatal brain tumour. We identified C1q/TNF-related protein 8 (CTRP8) as a novel agonist of the RXFP1 receptor. CTRP8 enhanced the motility and matrix invasion of GB, and this involved PKC-mediated up-regulation of cathepsin B, a marker for poor prognosis in GB patients. We conclude that the absence of relaxin isoforms does not preclude the activation of the RXFP1 receptor, as the least known member of the CTRP family, CTRP8, can effectively target and activate RXFP1 receptors. LINKED ARTICLES: This article is part of a themed section on Recent Progress in the Understanding of Relaxin Family Peptides and their Receptors. To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v174.10/issuetoc.

Indexed as

Signal TransductionAdiponectinHumansNeoplasmsProtein ConformationReceptors, G-Protein-CoupledReceptors, PeptideRelaxinAdiponectinC1QTNF8 protein, humanReceptors, G-Protein-CoupledReceptors, PeptideRelaxinRXFP1 protein, human

Identifiers

PMID27443788
PMCPMC5406291

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.