Evidence map›Paper›PMID 25236394›Full record

ReviewCell death and differentiation2015

Exosomes as divine messengers: are they the Hermes of modern molecular oncology?

C Braicu, C Tomuleasa, P Monroig, A Cucuianu, I Berindan-Neagoe, G A Calin

Open access · bronzeAbstract readReview
In one paragraph

Review in Cell death and differentiation, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 159 papers.

0numbers the graph read from it
0cells of the map it votes in
159citing papers in PubMed
13.2field-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

159 citing papers in PubMed, 306 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Exosomes promise better bone regeneration.Regenerative therapy · 2025
    Review
  6. Review
  7. Article
  8. Review
  9. Review
  10. Tumor microenvironment: new era in exosomal circRNA research - a bibliometric analysis.Extracellular vesicles and circulating nucleic acids · 2025
    Article
  11. Review
  12. Review
  13. Article
  14. Review
  15. Review
  16. Exosome Mediated Cell-Cell Crosstalk in Tissue Injury and Repair.Results and problems in cell differentiation · 2024
    Review
  17. Review
  18. Article
  19. Article
  20. Article

99 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

6 authors at 3 institutions in 2 countries.

C BraicuResearch Center for Functional Genomics and Translational Medicine, 'Iuliu Hatieganu' University of Medicine and Pharmacy, Cluj-Napoca, Romania.
C Tomuleasa1] Research Center for Functional Genomics and Translational Medicine, 'Iuliu Hatieganu' University of Medicine and Pharmacy, Cluj-Napoca, Romania [2] Department of Hematology, 'Ion Chiricuta' Oncology Institute, Cluj-Napoca, Romania.
P Monroig1] Department of Experimental Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA [2] University of Puerto Rico School of Medicine, San Juan, Puerto Rico.
A Cucuianu1] Department of Hematology, 'Ion Chiricuta' Oncology Institute, Cluj-Napoca, Romania [2] Department of Hematology, 'Iuliu Hatieganu' University of Medicine and Pharmacy, Cluj-Napoca, Romania.
I Berindan-Neagoe1] Research Center for Functional Genomics and Translational Medicine, 'Iuliu Hatieganu' University of Medicine and Pharmacy, Cluj-Napoca, Romania [2] Department of Immunology, 'Iuliu Hatieganu' University of Medicine and Pharmacy, Cluj-Napoca, Romania [3] Department of Functional Genomics and Experimental Pathology, 'Ion Chiricuta' Oncology Institute, Cluj-Napoca, Romania.
G A Calin1] Department of Experimental Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA [2] Center for RNA Interference and Non-Coding RNAs, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Iuliu Hațieganu University of Medicine and Pharmacy · ROThe University of Texas MD Anderson Cancer Center · USInstitute of Oncology Prof. Dr. Ion Chiricuta · RO

Funding

University of Texas M.D. Anderson Cancer SPORE-LeukemiaP50CA100632 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI SHPALL, ELIZABETH J · 2003 to 2023
$43.7M
Targeting the p53 pathway for reversal of oral premalignancyP50CA097007 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI MILLS, GORDON B. · 2002 to 2012
$26.1M
Protein-coding and non-coding RNA biomarkers for early detection of CLLR01CA182905 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI ABRUZZO, LYNNE V., CALIN, GEORGE A. · 2014 to 2018
$2.9M
Novel extra cellular RNA-based combinatorial RNA inhibition therapyUH2TR000943 · NCATS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI CALIN, GEORGE A., LOPEZ-BERESTEIN, GABRIEL · 2013 to 2014
$1.1M
NCATS NIH HHS 1UH2TR00943-01NCATS NIH HHS UH2 TR000943NCI NIH HHS 1R01 CA182905-01NCI NIH HHS P50 CA097007NCI NIH HHS P50 CA100632NCI NIH HHS R01 CA182905
6 · The paper itself

Abstract

Exosomes are cell-derived vesicles that convey key elements with the potential to modulate intercellular communication. They are known to be secreted from all types of cells, and are crucial messengers that can regulate cellular processes by 'trafficking' molecules from cells of one tissue to another. The exosomal content has been shown to be broad, composed of different types of cytokines, growth factors, proteins, or nucleic acids. Besides messenger RNA (mRNA) they can also contain noncoding transcripts such as microRNAs (miRNAs), which are small endogenous cellular regulators of protein expression. In diseases such as cancer, exosomes can facilitate tumor progression by altering their vesicular content and supplying the tumor niche with molecules that favor the progression of oncogenic processes such as proliferation, invasion and metastasis, or even drug resistance. The packaging of their molecular content is known to be tissue specific, a fact that makes them interesting tools in clinical diagnostics and ideal candidates for biomarkers. In the current report, we describe the main properties of exosomes and explain their involvement in processes such as cell differentiation and cell death. Furthermore, we emphasize the need of developing patient-targeted treatments by applying the conceptualization of exosomal-derived miRNA-based therapeutics.

Indexed as

ExosomesGene Expression Regulation, NeoplasticMicroRNAsNeoplasmsProtein BiosynthesisRNA, NeoplasmAnimalsCell DeathCell DifferentiationCell ProliferationHumansNeoplasm InvasivenessNeoplasm MetastasisMicroRNAsRNA, Neoplasm

Identifiers

PMID25236394
PMCPMC4262777
OpenAlexW1978283443

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.