Evidence map›Paper›PMID 20620173›Full record

ArticleBiochimica et biophysica acta2010

Posttranslational regulation of membrane type 1-matrix metalloproteinase (MT1-MMP) in mouse PTEN null prostate cancer cells: Enhanced surface expression and differential O-glycosylation of MT1-MMP.

Seaho Kim, Wei Huang, Emilio P Mottillo, Anjum Sohail, Yoon-Ah Ham, M Katie Conley-Lacomb, Chong Jai Kim, Guri Tzivion, Hyeong-Reh Choi Kim, Shihua Wang and 2 more

Open access · greenAbstract read
In one paragraph

Article in Biochimica et biophysica acta, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

16 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Review
  6. MicroRNA-29a activates a multi-component growth and invasion program in glioblastoma.Journal of experimental & clinical cancer research : CR · 2019
    Article
  7. PI3K: A Crucial Piece in the RAS Signaling Puzzle.Cold Spring Harbor perspectives in medicine · 2018
    Review
  8. Review
  9. Article
  10. Article
  11. Novel therapeutic targets for pancreatic cancer.World journal of gastroenterology · 2014
    Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. 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

12 authors at 2 institutions in 1 country.

Seaho KimDepartment of Pathology, School of Medicine, Wayne State University, Detroit, MI 48201, USA.
Wei Huang
Emilio P Mottillo
Anjum Sohail
Yoon-Ah Ham
M Katie Conley-Lacomb
Chong Jai Kim
Guri Tzivion
Hyeong-Reh Choi Kim
Shihua Wang
Yong Q Chen
Rafael Fridman
Wayne State University · USWake Forest University · US

Funding

Phospholipid Signaling in Fish oil-induced Growth Inhibition of Prostate CancerP01CA106742 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI CHEN, YONG Q · 2006 to 2010
$5.0M
REGULATION OF MATRIX METALLOPROTEINASE ACTIVATIONR01CA061986 · NCI · WAYNE STATE UNIVERSITY · PI FRIDMAN, RAFAEL A. · 1995 to 2015
$3.9M
Mechanisms of Fish Oil Supplement in Prevention of Pros*R01CA107668 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI CHEN, YONG Q · 2004 to 2014
$2.9M
NCI NIH HHS CA61986NCI NIH HHS P01 CA106742NCI NIH HHS P01CA106742NCI NIH HHS R01 CA061986NCI NIH HHS R01 CA107668NCI NIH HHS R01CA107668
6 · The paper itself

Abstract

Membrane type 1 (MT1)-matrix metalloproteinase (MT1-MMP) is a membrane-tethered MMP that has been shown to play a key role in promoting cancer cell invasion. MT1-MMP is highly expressed in bone metastasis of prostate cancer (PC) patients and promotes intraosseous tumor growth of PC cells in mice. The majority of metastatic prostate cancers harbor loss-of-function mutations or deletions of the tumor suppressor PTEN (phosphatase and tensin homologue deleted on chromosome ten). However, the role of PTEN inactivation in MT1-MMP expression in PC cells has not been examined. In this study, prostate epithelial cell lines derived from mice that are either heterozygous (PTEN(+/-)) or homozygous (PTEN(-/-)) for PTEN deletion or harboring a wild-type PTEN (PTEN(+/+)) were used to investigate the expression of MT1-MMP. We found that biallelic loss of PTEN is associated with posttranslational regulation of MT1-MMP protein in mouse PC cells. PTEN(-/-) PC cells display higher levels of MT1-MMP at the cell surface when compared to PTEN(+/+) and PTEN(+/-) cells and consequently exhibited enhanced migratory and collagen-invasive activities. MT1-MMP displayed by PTEN(-/-) cells is differentially O-glycosylated and exhibits a slow rate of turnover. MT1-MMP expression in PTEN(-/-) cells is under control of the PI3K/AKT signaling pathway, as determined using pharmacological inhibitors. Interestingly, rapamycin, an mTOR inhibitor, upregulates MT1-MMP expression in PTEN(+/+) cells via PI3K activity. Collectively, these data in a mouse prostate cell system uncover for the first time a novel and complex relationship between PTEN loss-mediated PI3K/AKT activation and posttranslational regulation of MT1-MMP, which may play a role in PC progression.

Indexed as

Protein Processing, Post-TranslationalAnimalsCell Line, TumorCell MembraneCell MovementEnzyme ActivationEnzyme PrecursorsEpithelial CellsGelatinasesGene Expression ProfilingGenotypeGlycosylationHumansImmunoblottingMaleMatrix Metalloproteinase 14Enzyme PrecursorsGelatinasesMatrix Metalloproteinase 14Phosphatidylinositol 3-KinasesprogelatinaseProto-Oncogene Proteins c-aktPTEN PhosphohydrolaseSirolimus

Identifiers

PMID20620173
PMCPMC2939279
OpenAlexW2104915842

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.