Evidence map›Paper›PMID 27440046›Full record

ArticleThe Journal of biological chemistry2016

Microvesicle Cargo and Function Changes upon Induction of Cellular Transformation.

Bridget T Kreger, Andrew L Dougherty, Kai Su Greene, Richard A Cerione, Marc A Antonyak

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
4.2field-weighted citation impact, top 6% 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

35 citing papers in PubMed, 54 citations in OpenAlex.

  1. Biogenesis and functional implications of extracellular vesicles in cancer metastasis.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2025
    Review
  2. Review
  3. Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. Cellular senescence, rejuvenation and potential immortality.Proceedings. Biological sciences · 2022
    Review
  12. Review
  13. Article
  14. Article
  15. The ins and outs of microvesicles.FASEB bioAdvances · 2021
    Review
  16. Article
  17. Extracellular Vesicles and Their Roles in Cancer Progression.Methods in molecular biology (Clifton, N.J.) · 2021
    Article
  18. Through the back door: Unconventional protein secretion.Cell surface (Amsterdam, Netherlands) · 2020
    Review
  19. Article
  20. [Progress in extracellular vesicle imaging methods].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2020
    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

5 authors at 1 institution in 2 countries.

Bridget T KregerFrom the Departments of Molecular Medicine and.
Andrew L DoughertyFrom the Departments of Molecular Medicine and.
Kai Su GreeneFrom the Departments of Molecular Medicine and.
Richard A CerioneFrom the Departments of Molecular Medicine and Chemistry and Chemical Biology, Cornell University, Ithaca, New York 14853 rac1@cornell.edu.
Marc A AntonyakFrom the Departments of Molecular Medicine and.
Laboratory of Molecular Genetics · PL

Funding

Overall (pp. 40-62)P41GM103485 · NIGMS · CORNELL UNIVERSITY · PI CERIONE, RICHARD A. · 2012 to 2018
$15.5M
Roles of Cdc42 and its signaling partners in cell growth and differentiationR01GM047458 · NIGMS · CORNELL UNIVERSITY ITHACA · PI CERIONE, RICHARD A. · 1992 to 2016
$5.6M
RECONSTITUTION OF GROWTH FACTOR RECEPTOR/TYROSINE KINASER01GM040654 · NIGMS · CORNELL UNIVERSITY ITHACA · PI CERIONE, RICHARD A. · 1988 to 2016
$5.6M
The unique roles of the GTP-binding/protein crosslinking enzyme transglutaminase-2 and signaling partners in aggressive cancersR01CA201402 · NCI · CORNELL UNIVERSITY · PI CERIONE, RICHARD A. · 2016 to 2024
$4.3M
New frontiers in extracellular signalingR35GM122575 · NIGMS · CORNELL UNIVERSITY · PI CERIONE, RICHARD A. · 2017 to 2021
$3.0M
NCI NIH HHS R01 CA201402NIGMS NIH HHS P41 GM103485NIGMS NIH HHS R01 GM040654NIGMS NIH HHS R01 GM047458NIGMS NIH HHS R35 GM122575
6 · The paper itself

Abstract

Extracellular vesicles (EVs), including exosomes and microvesicles (MVs), have emerged as a major form of intercellular communication, playing important roles in several physiological processes and diseases, including cancer. EVs generated by cancer cells contain a variety of proteins and RNA species that can be transferred between cancer cells as well as between cancer and non-transformed (normal) cells, thereby impacting a number of aspects of cancer progression. Here we show how oncogenic transformation influences the biogenesis and function of EVs using a mouse embryonic fibroblast (MEF) cell line that can be induced to express an oncogenic form of diffuse B cell lymphoma (Dbl). Although MEFs induced to express onco-Dbl generated a similar amount of MVs as uninduced control cells, we found that MVs isolated from onco-Dbl-transformed cells contain a unique signaling protein, the ubiquitously expressed non-receptor tyrosine kinase focal adhesion kinase. The addition of MVs isolated from MEFs expressing onco-Dbl to cultures of fibroblasts strongly promoted their survival and induced their ability to grow under anchorage-independent conditions, outcomes that could be reversed by knocking down focal adhesion kinase and depleting it from the MVs or by inhibiting its kinase activity using a specific inhibitor. We then showed the same to be true for MVs isolated from aggressive MDAMB231 breast cancer cells. Together, these findings demonstrate that the induction of oncogenic transformation gives rise to MVs, which uniquely contain a signaling protein kinase that helps propagate the transformed phenotype and thus may offer a specific diagnostic marker of malignant disease.

Indexed as

AnimalsCell-Derived MicroparticlesCell Line, TumorCell Transformation, NeoplasticEmbryo, MammalianExosomesFemaleGene Expression Regulation, NeoplasticGuanine Nucleotide Exchange FactorsHumansMiceNeoplasmsNIH 3T3 CellsProto-Oncogene ProteinsGuanine Nucleotide Exchange FactorsMCF2 protein, humanMcf2 protein, mouseProto-Oncogene Proteinscell signalingexosome (vesicle)extracellular vesiclesfocal adhesion kinase (FAK)intercellular communicationmicroparticlesmicrovesiclesPTK2 protein tyrosine kinase 2 (PTK2)transformation

Identifiers

PMID27440046
PMCPMC5025668
OpenAlexW2481255288

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.