Evidence map›Paper›PMID 24434559›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2014

GRK3 is essential for metastatic cells and promotes prostate tumor progression.

Wenliang Li, Nanping Ai, Suming Wang, Nandita Bhattacharya, Vladimir Vrbanac, Michael Collins, Sabina Signoretti, Yanhui Hu, Frederick M Boyce, Karsten Gravdal and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

32 citing papers in PubMed, 50 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. G protein-coupled receptor signaling: transducers and effectors.American journal of physiology. Cell physiology · 2022
    Review
  11. Article
  12. Article
  13. CRISPR Screen Contributes to Novel Target Discovery in Prostate Cancer.International journal of molecular sciences · 2021
    Review
  14. Article
  15. The GRKs Reactome: Role in Cell Biology and Pathology.International journal of molecular sciences · 2021
    Review
  16. Review
  17. Article
  18. Review
  19. 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

15 authors at 8 institutions in 2 countries.

Wenliang LiBrown Foundation Institute of Molecular Medicine, University of Texas Health Science Center at Houston, Houston, TX 77030.
Nanping Ai
Suming Wang
Nandita Bhattacharya
Vladimir Vrbanac
Michael Collins
Sabina Signoretti
Yanhui Hu
Frederick M Boyce
Karsten Gravdal
Ole J Halvorsen
Hawa Nalwoga
Lars A Akslen
Ed Harlow
Randolph S Watnick
Harvard University · USBoston Children's Hospital · USBrigham and Women's Hospital · USHaukeland University Hospital · NOUniversity of Bergen · NOBrown Foundation · USThe University of Texas Health Science Center at Houston · USTufts University · US

Funding

TUMOR DORMANCY INDUCED BY BLOCKED ANGIOGENESISP01CA045548 · NCI · CHILDREN'S HOSPITAL BOSTON · PI FOLKMAN, JUDAH · 1987 to 2011
$22.6M
Molecular mechanisms of tumor-initiated premetastatic niche formation in lung strR01CA135417 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI MITTAL, VIVEK, WATNICK, RANDOLPH S · 2010 to 2014
$2.6M
Mechanisms regulating prostate epithelium maintenance and regenerationR01DK089975 · NIDDK · BRIGHAM AND WOMEN'S HOSPITAL · PI SIGNORETTI, SABINA · 2010 to 2014
$1.9M
NCI NIH HHS P01 CA045548NCI NIH HHS R01 CA135417NIDDK NIH HHS 1R01DK089975NIDDK NIH HHS R01 DK089975
6 · The paper itself

Abstract

The biochemical mechanisms that regulate the process of cancer metastasis are still poorly understood. Because kinases, and the signaling pathways they comprise, play key roles in regulation of many cellular processes, we used an unbiased RNAi in vitro screen and a focused cDNA in vivo screen against human kinases to identify those with previously undocumented roles in metastasis. We discovered that G-protein-coupled receptor kinase 3 (GRK3; or β-adrenergic receptor kinase 2) was not only necessary for survival and proliferation of metastatic cells, but also sufficient to promote primary prostate tumor growth and metastasis upon exogenous expression in poorly metastatic cells in mouse xenograft models. Mechanistically, we found that GRK3 stimulated angiogenesis, at least in part through down-regulation of thrombospondin-1 and plasminogen activator inhibitor type 2. Furthermore, GRK3 was found to be overexpressed in human prostate cancers, especially in metastatic tumors. Taken together, these data suggest that GRK3 plays an important role in prostate cancer progression and metastasis.

Indexed as

Neoplasm MetastasisCell ProliferationDisease ProgressionG-Protein-Coupled Receptor Kinase 3HumansMalePlasminogen Activator Inhibitor 2Prostatic NeoplasmsThrombospondin 1G-Protein-Coupled Receptor Kinase 3GRK3 protein, humanPlasminogen Activator Inhibitor 2Thrombospondin 1ADRBK2essential kinasesfunctional screensPAI-2TSP-1

Identifiers

PMID24434559
PMCPMC3910602
OpenAlexW2080237382

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.