Evidence map›Paper›PMID 26583135›Full record

ReviewBioMed research international2015

Role of Extracellular Vesicles in Hematological Malignancies.

Stefania Raimondo, Chiara Corrado, Lavinia Raimondi, Giacomo De Leo, Riccardo Alessandro

Open access · hybridAbstract readReview
In one paragraph

Review in BioMed research international, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

19 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. Article
  11. Review
  12. Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. 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

5 authors at 3 institutions in 1 country.

Stefania RaimondoDipartimento di Biopatologia e Biotecnologie Mediche, Università degli Studi di Palermo, Sezione di Biologia e Genetica, Via Divisi 83, 90133 Palermo, Italy.
Chiara CorradoDipartimento di Biopatologia e Biotecnologie Mediche, Università degli Studi di Palermo, Sezione di Biologia e Genetica, Via Divisi 83, 90133 Palermo, Italy.
Lavinia RaimondiLaboratorio di Ingegneria Tissutale-Piattaforme Innovative per l'Ingegneria Tessutale (PON01-00829), Istituto Ortopedico Rizzoli, 90133 Palermo, Italy.
Giacomo De LeoDipartimento di Biopatologia e Biotecnologie Mediche, Università degli Studi di Palermo, Sezione di Biologia e Genetica, Via Divisi 83, 90133 Palermo, Italy.
Riccardo AlessandroDipartimento di Biopatologia e Biotecnologie Mediche, Università degli Studi di Palermo, Sezione di Biologia e Genetica, Via Divisi 83, 90133 Palermo, Italy ; Institute of Biomedicine and Molecular Immunology (IBIM), National Research Council of Italy, 90146 Palermo, Italy.
University of Palermo · ITIstituto di Biomedicina e di Immunologia Molecolare Alberto Monroy · ITIstituto Ortopedico Rizzoli · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In recent years the role of tumor microenvironment in the progression of hematological malignancies has been widely recognized. Recent studies have focused on how cancer cells communicate within the microenvironment. Among several factors (cytokines, growth factors, and ECM molecules), a key role has been attributed to extracellular vesicles (EV), released from different cell types. EV (microvesicles and exosomes) may affect stroma remodeling, host cell functions, and tumor angiogenesis by inducing gene expression modulation in target cells, thus promoting cancer progression and metastasis. Microvesicles and exosomes can be recovered from the blood and other body fluids of cancer patients and contain and deliver genetic and proteomic contents that reflect the cell of origin, thus constituting a source of new predictive biomarkers involved in cancer development and serving as possible targets for therapies. Moreover, due to their specific cell-tropism and bioavailability, EV can be considered natural vehicles suitable for drug delivery. Here we will discuss the recent advances in the field of EV as actors in hematological cancer progression, pointing out the role of these vesicles in the tumor-host interplay and in their use as biomarkers for hematological malignancies.

Indexed as

ExosomesExtracellular VesiclesGene Expression Regulation, NeoplasticHematologic NeoplasmsHumansNeovascularization, PathologicProteomicsTumor Microenvironment

Identifiers

PMID26583135
PMCPMC4637071
OpenAlexW2138929080

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.