Extracellular vesicles in hematological malignancies.
Antineoplastic Agents
/ pharmacology
Biomarkers, Tumor
/ antagonists & inhibitors
Bone Marrow
/ metabolism
Cell Communication
Disease Progression
Drug Resistance, Multiple
/ drug effects
Drug Resistance, Neoplasm
/ drug effects
Extracellular Vesicles
/ drug effects
Feedback, Physiological
Hematologic Neoplasms
/ diagnosis
Humans
MicroRNAs
/ antagonists & inhibitors
Neovascularization, Pathologic
/ pathology
Signal Transduction
/ drug effects
Transforming Growth Factor beta1
/ antagonists & inhibitors
Tumor Microenvironment
Exosomes
cell-to-cell transport
microvesicles
Journal
Leukemia & lymphoma
ISSN: 1029-2403
Titre abrégé: Leuk Lymphoma
Pays: United States
ID NLM: 9007422
Informations de publication
Date de publication:
01 2019
01 2019
Historique:
pubmed:
11
5
2018
medline:
1
1
2020
entrez:
11
5
2018
Statut:
ppublish
Résumé
Extracellular vesicles (EVs) act as transporters that carry regulatory molecules between cells in physiologic and pathologic states; therefore, they play a crucial role in thrombosis, inflammation, angiogenesis, vascular dysfunction and other processes that affect the course of hematologic diseases. Within the tumor microenvironment, for example the leukemic bone marrow, EVs-mediated signaling may direct the activities of surrounding cells and act as a positive feedback loop that contributes to cancer progression. The importance of EVs in hematological malignancies is also attributed to their involvement in development of multidrug resistance and the hypercoagulable state related to hematologic disorders, which may be partially influenced by an increase in the total number of EVs. In this review, we focused on the role of EVs in hematologic malignancies and in particular on their influence on the BM microenvironment, their role in angiogenesis and the possible use of EVs as biomarkers of disease progression and drug resistance.
Identifiants
pubmed: 29745272
doi: 10.1080/10428194.2018.1459606
doi:
Substances chimiques
Antineoplastic Agents
0
Biomarkers, Tumor
0
MicroRNAs
0
TGFB1 protein, human
0
Transforming Growth Factor beta1
0
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM