Evidence map›Paper›PMID 24432300›Full record

ArticleAnnals of translational medicine2013

Functional role of microvesicles in gastrointestinal malignancies.

Kelly McDaniel, Robert Correa, Tianhao Zhou, Christopher Johnson, Heather Francis, Shannon Glaser, Julie Venter, Gianfranco Alpini, Fanyin Meng

Open access · greenAbstract read
In one paragraph

Article in Annals of translational medicine, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

10 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Review
  3. Tracking tools of extracellular vesicles for biomedical research.Frontiers in bioengineering and biotechnology · 2022
    Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. RKIP inhibits gastric cancer cell survival and invasion by regulating the expression of HMGA2 and OPN.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2014
    Article
  10. miR-34a regulates cisplatin-induce gastric cancer cell death by modulating PI3K/AKT/survivin pathway.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2014
    Article
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

9 authors at 4 institutions in 2 countries.

Kelly McDanielScott & White Digestive Disease Research Center, Scott & White Healthcare, Temple, Texas 76S04, USA.
Robert CorreaScott & White Digestive Disease Research Center, Scott & White Healthcare, Temple, Texas 76S04, USA.
Tianhao ZhouScott & White Digestive Disease Research Center, Scott & White Healthcare, Temple, Texas 76S04, USA ; School of Chemistry and Chemical Engineering, Shanghai University of Engineering Science, Shanghai 201620, China.
Christopher JohnsonScott & White Digestive Disease Research Center, Scott & White Healthcare, Temple, Texas 76S04, USA ; Research Division, Central Texas Veterans Health Care System, Temple, TX, USA ; Department of Medicine, Division of Gastroenterology, Texas A&M Health Science Center, College of Medicine, Temple, TX 76S04, USA.
Heather FrancisScott & White Digestive Disease Research Center, Scott & White Healthcare, Temple, Texas 76S04, USA ; Research Division, Central Texas Veterans Health Care System, Temple, TX, USA ; Department of Medicine, Division of Gastroenterology, Texas A&M Health Science Center, College of Medicine, Temple, TX 76S04, USA.
Shannon GlaserScott & White Digestive Disease Research Center, Scott & White Healthcare, Temple, Texas 76S04, USA ; Research Division, Central Texas Veterans Health Care System, Temple, TX, USA ; Department of Medicine, Division of Gastroenterology, Texas A&M Health Science Center, College of Medicine, Temple, TX 76S04, USA.
Julie VenterDepartment of Medicine, Division of Gastroenterology, Texas A&M Health Science Center, College of Medicine, Temple, TX 76S04, USA.
Gianfranco AlpiniScott & White Digestive Disease Research Center, Scott & White Healthcare, Temple, Texas 76S04, USA ; Research Division, Central Texas Veterans Health Care System, Temple, TX, USA ; Department of Medicine, Division of Gastroenterology, Texas A&M Health Science Center, College of Medicine, Temple, TX 76S04, USA.
Fanyin MengScott & White Digestive Disease Research Center, Scott & White Healthcare, Temple, Texas 76S04, USA ; Research Division, Central Texas Veterans Health Care System, Temple, TX, USA ; Department of Medicine, Division of Gastroenterology, Texas A&M Health Science Center, College of Medicine, Temple, TX 76S04, USA.
Central Texas Veterans Health Care System · USWhite Clinic · PTBaylor Scott & White Health · USTemple College · US

Funding

Regulation of Bile Duct Growth in Bile Duct Ligated RatsR01DK062975 · NIDDK · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI ALPINI, GIANFRANCO D, GLASER, SHANNON STROUD · 2005 to 2014
$1.9M
Role of Sensory Neuropeptides in the Regulation of Biliary FunctionR01DK076898 · NIDDK · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI ALPINI, GIANFRANCO D, GLASER, SHANNON STROUD · 2008 to 2016
$1.8M
NIDDK NIH HHS R01 DK062975NIDDK NIH HHS R01 DK076898
6 · The paper itself

Abstract

Microvesicles (MVs) are derived from the plasma membrane and are released into the intracellular space by outward budding and fission of the plasma membrane of cells. Various studies have shown high regulation of microvesicles shedding from cells widespread throughout the body, often involving cancerous cells. MVs are originated from the endosomal membrane compartment, and after fusion with the plasma membrane, they are shed from the cell surface of activated cells. Therefore, microvesicles may be secreted by activated malignant and normal cells and play a role in cellular communication during cancer development. Microvesicles are found in many biological fluids in the body and have been demonstrated to receive their functionality from the parent cell from which they are derived. MVs facilitate the transfer of proteins and other molecules, thereby allowing for interaction with cells and tissues far away from the originating cell. This functionality has caused researchers to view microvesicles as a primary component of tumor progression and development. This commentary summarizes recent literature on the properties and biogenesis of microvesicles, and their influence on gastrointestinal tumor progression.

Indexed as

gastrointestinal malignanciesMicrovesicles (MVs)

Identifiers

PMID24432300
PMCPMC3890379
OpenAlexW32222551

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.