Evidence map›Paper›PMID 23856248›Full record

ArticleCancer research2013

PTK6 activation at the membrane regulates epithelial-mesenchymal transition in prostate cancer.

Yu Zheng, Zebin Wang, Wenjun Bie, Patrick M Brauer, Bethany E Perez White, Jing Li, Veronique Nogueira, Pradip Raychaudhuri, Nissim Hay, Debra A Tonetti and 3 more

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in Cancer research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

36 citing papers in PubMed, 59 citations in OpenAlex.

  1. Novel Functionalized Pyrrolopyridines to Target Brk.Molecules (Basel, Switzerland) · 2026
    Article
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  17. Review
  18. Targeting protein tyrosine kinase 6 in cancer.Biochimica et biophysica acta. Reviews on cancer · 2020
    Review
  19. Article
  20. Protein tyrosine kinase 6 signaling in prostate cancer.American journal of clinical and experimental urology · 2020
    Review
4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

13 authors at 2 institutions in 1 country.

Yu ZhengDepartment of Biochemistry, Biopharmaceutical Sciences, and Pathology, University of Illinois at Chicago, Chicago, IL 60607, USA.
Zebin Wang
Wenjun Bie
Patrick M Brauer
Bethany E Perez White
Jing Li
Veronique Nogueira
Pradip Raychaudhuri
Nissim Hay
Debra A Tonetti
Virgilia Macias
André Kajdacsy-Balla
Angela L Tyner
University of Illinois Chicago · USJesse Brown VA Medical Center · US

Funding

PI3K/PTEN/Akt signaling and the genesis of cancerR01CA090764 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI Nissim Hay · 2001 to 2026
$9.4M
ISOLATION OF GENETIC MARKERS FOR INTESTINAL CRYPT CELLSR01DK044525 · NIDDK · UNIVERSITY OF ILLINOIS AT CHICAGO · PI TYNER, ANGELA L · 1993 to 2016
$4.8M
BRK/Sik Tyrosine Kinase Signaling in the ProstateR01DK068503 · NIDDK · UNIVERSITY OF ILLINOIS AT CHICAGO · PI TYNER, ANGELA L · 2005 to 2009
$1.4M
ISOLATION OF GENETIC MARKERS FOR INTESTINAL CRYPT CELLSR55DK044525 · NIDDK · UNIVERSITY OF ILLINOIS AT CHICAGO · PI TYNER, ANGELA L · 1992 to 1992
–
NCI NIH HHS R01 CA090764NIDDK NIH HHS DK44525NIDDK NIH HHS R01 DK044525NIDDK NIH HHS R01 DK068503
6 · The paper itself

Abstract

The intracellular tyrosine kinase protein tyrosine kinase 6 (PTK6) lacks a membrane-targeting SH4 domain and localizes to the nuclei of normal prostate epithelial cells. However, PTK6 translocates from the nucleus to the cytoplasm in human prostate tumor cells. Here, we show that while PTK6 is located primarily within the cytoplasm, the pool of active PTK6 in prostate cancer cells localizes to membranes. Ectopic expression of membrane-targeted active PTK6 promoted epithelial-mesenchymal transition in part by enhancing activation of AKT, thereby stimulating cancer cell migration and metastases in xenograft models of prostate cancer. Conversely, siRNA-mediated silencing of endogenous PTK6 promoted an epithelial phenotype and impaired tumor xenograft growth. In mice, PTEN deficiency caused endogenous active PTK6 to localize at membranes in association with decreased E-cadherin expression. Active PTK6 was detected at membranes in some high-grade human prostate tumors, and PTK6 and E-cadherin expression levels were inversely correlated in human prostate cancers. In addition, high levels of PTK6 expression predicted poor prognosis in patients with prostate cancer. Our findings reveal novel functions for PTK6 in the pathophysiology of prostate cancer, and they define this kinase as a candidate therapeutic target. Cancer Res; 73(17); 5426-37. ©2013 AACR.

Indexed as

Epithelial-Mesenchymal TransitionAnimalsApoptosisBlotting, WesternCadherinsCell Line, TumorCell MembraneCell MovementCell NucleusCell ProliferationCytoplasmHumansImmunoprecipitationLiver NeoplasmsLung NeoplasmsMaleCadherinsNeoplasm ProteinsProtein-Tyrosine KinasesProto-Oncogene Proteins c-aktPTEN PhosphohydrolasePten protein, mousePTK6 protein, humanRNA, MessengerRNA, Small Interfering

Identifiers

PMID23856248
PMCPMC3766391
OpenAlexW2099473143

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.