Evidence map›Paper›PMID 24174371›Full record

ArticleThe Prostate2014

Src-dependent Tks5 phosphorylation regulates invadopodia-associated invasion in prostate cancer cells.

Karen L Burger, Brian S Learman, Amy K Boucherle, S Joseph Sirintrapun, Scott Isom, Begoña Díaz, Sara A Courtneidge, Darren F Seals

Open access · greenAbstract read
In one paragraph

Article in The Prostate, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

43 citing papers in PubMed, 76 citations in OpenAlex.

  1. Article
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  3. Review
  4. Article
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  8. Article
  9. The Role of TKS5 in Chromosome Stability and Bladder Cancer Progression.International journal of molecular sciences · 2022
    Article
  10. Article
  11. Review
  12. Review
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  15. Observational
  16. Article
  17. Observational
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  19. Article
  20. The Circular RNA circSKA3 Binds Integrin β1 to Induce Invadopodium Formation Enhancing Breast Cancer Invasion.Molecular therapy : the journal of the American Society of Gene Therapy · 2020
    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

8 authors at 3 institutions in 1 country.

Karen L BurgerDepartment of Cancer Biology, Wake Forest Comprehensive Cancer Center, Wake Forest School of Medicine, Winston-Salem, North Carolina.
Brian S Learman
Amy K Boucherle
S Joseph Sirintrapun
Scott Isom
Begoña Díaz
Sara A Courtneidge
Darren F Seals
Wake Forest University · USSanford Burnham Prebys Medical Discovery Institute · USAppalachian State University · US

Funding

Tumor Microenvironment and Cancer ImmunologyP30CA030199 · NCI · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI Michael Jackson · 1985 to 2026
$107.2M
Tumor Tissue CoreP30CA012197 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Ruben A. Mesa · 1985 to 2026
$55.4M
Training Program in Cancer BiologyT32CA079448 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI KRIDEL, STEVEN J. · 2000 to 2014
$6.5M
Kinases as therapeutic targets for cancer progressionR01CA154002 · NCI · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI COURTNEIDGE, SARA A · 2011 to 2015
$1.9M
Generation and utility of NADPH oxidase inhibitorsR01CA153065 · NCI · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI COURTNEIDGE, SARA A · 2010 to 2012
$1.2M
NCI NIH HHS CA153065NCI NIH HHS CA154002NCI NIH HHS P30 CA012197NCI NIH HHS P30 CA030199NCI NIH HHS R01 CA153065NCI NIH HHS R01 CA154002NCI NIH HHS T32 CA079448NCI NIH HHS T32-CA079448
6 · The paper itself

Abstract

backgroundThe Src tyrosine kinase substrate and adaptor protein Tks5 had previously been implicated in the invasive phenotype of normal and transformed cell types via regulation of cytoskeletal structures called podosomes/invadopodia. The role of Src-Tks5 signaling in invasive prostate cancer, however, had not been previously evaluated.

methodsWe measured the relative expression of Tks5 in normal (n = 20) and cancerous (n = 184, from 92 patients) prostate tissue specimens by immunohistochemistry using a commercially available tumor microarray. We also manipulated the expression and activity of wild-type and mutant Src and Tks5 constructs in the LNCaP and PC-3 prostate cancer cell lines in order to ascertain the role of Src-Tks5 signaling in invadopodia development, matrix-remodeling activity, motility, and invasion.

resultsOur studies demonstrated that Src was activated and Tks5 upregulated in high Gleason score prostate tumor specimens and in invasive prostate cancer cell lines. Remarkably, overexpression of Tks5 in LNCaP cells was sufficient to induce invadopodia formation and associated matrix degradation. This Tks5-dependent increase in invasive behavior further depended on Src tyrosine kinase activity and the phosphorylation of Tks5 at tyrosine residues 557 and 619. In PC-3 cells we demonstrated that Tks5 phosphorylation at these sites was necessary and sufficient for invadopodia-associated matrix degradation and invasion.

conclusionsOur results suggest a general role for Src-Tks5 signaling in prostate tumor progression and the utility of Tks5 as a marker protein for the staging of this disease.

Indexed as

Adaptor Proteins, Vesicular TransportAdenocarcinomaBiomarkers, TumorCase-Control StudiesCell Line, TumorCell MovementCytoskeletonDisease ProgressionHumansImmunohistochemistryMalePhosphorylationProstatic NeoplasmsSignal Transductionsrc-Family KinasesAdaptor Proteins, Vesicular TransportBiomarkers, TumorSH3PXD2A protein, humansrc-Family Kinasesbiomarkercytoskeletonmetastasismotilitypodosome

Identifiers

PMID24174371
PMCPMC4083496
OpenAlexW2100426671

What OpenQuestion holds

Textmetadata
LicenceTDM
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.