Evidence map›Paper›PMID 26959113›Full record

ArticleOncotarget2016

Integrin-linked kinase activity modulates the pro-metastatic behavior of ovarian cancer cells.

Lana Bruney, Yueying Liu, Anne Grisoli, Matthew J Ravosa, M Sharon Stack

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
2.7field-weighted citation impact, top 11% 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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 33 citations in OpenAlex.

  1. Pooled it
  2. Review
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  7. Cytoplasmic Tail of MT1-MMP: A Hub of MT1-MMP Regulation and Function.International journal of molecular sciences · 2023
    Review
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  17. LncRNA MEG3 impacts proliferation, invasion, and migration of ovarian cancer cells through regulating PTEN.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2018
    Article
  18. Article
  19. Review
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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

5 authors at 3 institutions in 1 country.

Lana BruneyDepartment of Medical Physiology & Pharmacology, University of Missouri School of Medicine, Columbia, MO, USA.
Yueying LiuHarper Cancer Research Institute, University of Notre Dame, South Bend, IN, USA.
Anne GrisoliHarper Cancer Research Institute, University of Notre Dame, South Bend, IN, USA.
Matthew J RavosaBiological Sciences, University of Notre Dame, Notre Dame, IN, USA.
M Sharon StackDepartment of Medical Physiology & Pharmacology, University of Missouri School of Medicine, Columbia, MO, USA.
Cancer Research Institute · USUniversity of Notre Dame · USUniversity of Missouri · US

Funding

Receptor Cross-Talk in Early Metastatic DisseminationR01CA109545 · NCI · UNIVERSITY OF NOTRE DAME · PI STACK, MARY SHARON · 2006 to 2022
$4.3M
REGULATION OF OVARIAN CARCINOMA PROTEINASESR01CA086984 · NCI · UNIVERSITY OF NOTRE DAME · PI STACK, MARY SHARON · 2000 to 2014
$3.8M
Integrin Linked Kinase and Ovarian Cancer MetastasisF31CA159804 · NCI · UNIVERSITY OF MISSOURI-COLUMBIA · PI BRUNEY, LANA Y · 2011 to 2013
$86k
NCI NIH HHS F31 CA159804NCI NIH HHS R01 CA086984NCI NIH HHS R01 CA109545
6 · The paper itself

Abstract

Epithelial ovarian cancer (EOC) is the most fatal gynecologic cancer in the U.S., resulting in >14,000 deaths/year. Most women are diagnosed at late stage with widely disseminated intra-peritoneal metastatic disease, resulting in a 5-year survival rate of <30%. EOCs spread via direct extension and exfoliation into the peritoneal cavity, adhesion to peritoneal mesothelial cells, mesothelial cell retraction to expose sub-mseothelial matrix and anchoring in the type I collagen-rich matrix to generate secondary lesions. As a molecular-level understanding of EOC metastasis may identify novel therapeutic targets, the current study evaluated the expression and activity of integrin-linked kinase (ILK), a Ser/Thr protein kinase activated upon integrin-mediated adhesion. Results show that ILK is co-expressed in EOC with the pro-metastatic enzyme membrane type 1 matrix metalloproteinase (MT1-MMP) and catalyzed phosphorylation of the cytoplasmic tail of the proteinase. Downregulation of ILK expression or activity reduced adhesion to and invasion of collagen gels and organotypic meso-mimetic cultures. As an initial early event in EOC metastasis is integrin-mediated adhesion, these results suggest that further evaluation of ILK inhibitors as anti-metastatic agents in EOC is warranted.

Indexed as

Carcinoma, Ovarian EpithelialCell AdhesionCell Line, TumorFemaleHumansMatrix Metalloproteinase 14Neoplasm InvasivenessNeoplasms, Glandular and EpithelialOvarian NeoplasmsProtein Serine-Threonine KinasesScaffold Protein ILKMatrix Metalloproteinase 14MMP14 protein, humanProtein Serine-Threonine KinasesScaffold Protein ILKintegrinintegrin linked kinasemembrane type 1 matrix metalloproteinasemetastasisovarian cancer

Identifiers

PMID26959113
PMCPMC5008337
OpenAlexW2293432961

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.