Evidence map›Paper›PMID 20445011›Full record

ReviewJournal of cell science2010

Microvesicles: mediators of extracellular communication during cancer progression.

Vandhana Muralidharan-Chari, James W Clancy, Alanna Sedgwick, Crislyn D'Souza-Schorey

Abstract readReview
In one paragraph

Review in Journal of cell science, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 523 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
523citing papers in PubMed, 1 pooled it
20.3field-weighted citation impact, top 1% 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

523 citing papers in PubMed, 1 synthesis or guideline pooled it, 935 citations in OpenAlex.

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463 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

4 authors at 1 institution in 1 country.

Vandhana Muralidharan-ChariDepartment of Biological Sciences, University of Notre Dame, Notre Dame, IN 46556-0369, USA.
James W Clancy
Alanna Sedgwick
Crislyn D'Souza-Schorey
University of Notre Dame · US

Funding

Molecular Mechanisms of Cell InvasionR01CA115316 · NCI · UNIVERSITY OF NOTRE DAME · PI D'SOUZA-SCHOREY, CRISLYN · 2011 to 2016
$1.5M
Molecular Mechanisms of Cell InvasionR56CA115316 · NCI · UNIVERSITY OF NOTRE DAME · PI D'SOUZA-SCHOREY, CRISLYN · 2007 to 2008
$420k
NCI NIH HHS R01 CA115316NCI NIH HHS R56 CA115316
6 · The paper itself

Abstract

Microvesicles are generated by the outward budding and fission of membrane vesicles from the cell surface. Recent studies suggest that microvesicle shedding is a highly regulated process that occurs in a spectrum of cell types and, more frequently, in tumor cells. Microvesicles have been widely detected in various biological fluids including peripheral blood, urine and ascitic fluids, and their function and composition depend on the cells from which they originate. By facilitating the horizontal transfer of bioactive molecules such as proteins, RNAs and microRNAs, they are now thought to have vital roles in tumor invasion and metastases, inflammation, coagulation, and stem-cell renewal and expansion. This Commentary summarizes recent literature on the properties and biogenesis of microvesicles and their potential role in cancer progression.

Indexed as

Cell CommunicationAnimalsBiomarkers, TumorBlood CoagulationCell-Derived MicroparticlesCell Transformation, NeoplasticDisease ProgressionDrug Resistance, NeoplasmHumansLipid MetabolismNeoplasm InvasivenessNeoplasmsNeovascularization, PathologicOncogenesTumor EscapeBiomarkers, Tumor

Identifiers

PMID20445011
PMCPMC2864708
OpenAlexW1969002010

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.