Role of non-coding RNA networks in leukemia progression, metastasis and drug resistance.
Cancer
Chromatin
Circular RNAs
Drug resistance
Epigenetics
Gene regulation
Long non-coding RNAs
Metastasis
MicroRNAs
Signaling pathways
Journal
Molecular cancer
ISSN: 1476-4598
Titre abrégé: Mol Cancer
Pays: England
ID NLM: 101147698
Informations de publication
Date de publication:
12 03 2020
12 03 2020
Historique:
received:
15
12
2019
accepted:
02
03
2020
entrez:
14
3
2020
pubmed:
14
3
2020
medline:
3
2
2021
Statut:
epublish
Résumé
Early-stage detection of leukemia is a critical determinant for successful treatment of the disease and can increase the survival rate of leukemia patients. The factors limiting the current screening approaches to leukemia include low sensitivity and specificity, high costs, and a low participation rate. An approach based on novel and innovative biomarkers with high accuracy from peripheral blood offers a comfortable and appealing alternative to patients, potentially leading to a higher participation rate.Recently, non-coding RNAs due to their involvement in vital oncogenic processes such as differentiation, proliferation, migration, angiogenesis and apoptosis have attracted much attention as potential diagnostic and prognostic biomarkers in leukemia. Emerging lines of evidence have shown that the mutational spectrum and dysregulated expression of non-coding RNA genes are closely associated with the development and progression of various cancers, including leukemia. In this review, we highlight the expression and functional roles of different types of non-coding RNAs in leukemia and discuss their potential clinical applications as diagnostic or prognostic biomarkers and therapeutic targets.
Identifiants
pubmed: 32164715
doi: 10.1186/s12943-020-01175-9
pii: 10.1186/s12943-020-01175-9
pmc: PMC7069174
doi:
Substances chimiques
Biomarkers, Tumor
0
RNA, Long Noncoding
0
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
57Commentaires et corrections
Type : ErratumIn
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