Evidence map›Paper›PMID 10442635›Full record

ArticleOncogene1999

An invasion-related complex of cortactin, paxillin and PKCmu associates with invadopodia at sites of extracellular matrix degradation.

E T Bowden, M Barth, D Thomas, R I Glazer, S C Mueller

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 154 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
154citing papers in PubMed, 1 pooled it
3.6field-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

154 citing papers in PubMed, 1 synthesis or guideline pooled it, 352 citations in OpenAlex.

  1. Pooled it
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  12. Article
  13. Invadopodia: clearing the way for cancer cell invasion.Annals of translational medicine · 2020
    Review
  14. Article
  15. Article
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94 more citing papers are in PubMed but not listed here.

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 2 institutions in 1 country.

E T BowdenDepartment of Cell Biology, Lombardi Cancer Center, Georgetown University Medical School, Washington, DC 20007, USA.
M Barth
D Thomas
R I Glazer
S C Mueller
Georgetown University · USGeorgetown University Medical Center · US

Funding

MECHANISMS OF HORMONAL MODULATION OF BREAST CANCER CELLR01DK048910 · NIDDK · GEORGETOWN UNIVERSITY · PI MUELLER, SUSETTE C · 1994 to 2004
$1.2M
MEMBRANE PROTEASES IN BREAST CANCER METASTASISR01CA061273 · NCI · GEORGETOWN UNIVERSITY · PI MUELLER, SUSETTE C · 1993 to 1996
–
MECHANISMS OF TUMOR CELL INVASIONR21CA062232 · NCI · GEORGETOWN UNIVERSITY · PI MUELLER, SUSETTE C · 1994 to 1995
–
NCI NIH HHS R01CA61273NCI NIH HHS R21CA62232NIDDK NIH HHS R01DK48910
6 · The paper itself

Abstract

Invasive breast cancer cells have the ability to extend membrane protrusions, invadopodia, into the extracellular matrix (ECM). These structures are associated with sites of active matrix degradation. The amount of matrix degradation associated with the activity of these membrane protrusions has been shown to directly correlate with invasive potential. We demonstrate here that microinjection of polyclonal anti-cortactin antibodies blocks matrix degradation at invadopodia supporting the hypothesis that cortactin has a direct role in invasive behavior. MDA-MB-231, invasive breast cancer cells were sheared from the surface of a gelatin matrix to isolate invadopodia. Cortactin, paxillin and protein kinase C (PKC) mu, a serine kinase, were co-immunoprecipitated as a complex from invadopodia-enriched membranes. We confirmed the subcellular distribution of these proteins by immunolocalization and Western blotting. We also determined that, in contrast to its presence in invasive cells, this complex of proteins was not detected in lysates from non-invasive cells that do not form invadopodia. Taken together, these data suggest that the formation of this cortactin-containing complex correlates with cellular invasiveness. We hypothesize that this complex of molecules has a role in the formation and function of invadopodia during cellular invasion.

Indexed as

Neoplasm InvasivenessActinsBreast NeoplasmsCell Adhesion MoleculesCell MembraneCortactinCytoskeletal ProteinsExtracellular MatrixFemaleGelatinHumansIntegrin beta1Microfilament ProteinsMicroscopy, ElectronModels, BiologicalPaxillinActinsCell Adhesion MoleculesCortactinCTTN protein, humanCytoskeletal ProteinsGelatinIntegrin beta1Microfilament ProteinsPaxillinPhosphoproteinsProtein Kinase Cprotein kinase DPXN protein, human

Identifiers

PMID10442635
OpenAlexW1982036031

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.