Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/91979
PIRA download icon_1.1View/Download Full Text
Title: The tyrosine kinase-driven networks of novel long non-coding RNAs and their molecular targets in myeloproliferative neoplasms
Authors: Wong, NK 
Luo, S 
Chow, EYD
Meng, F 
Adesanya, A 
Sun, J 
Ma, HMH 
Jin, W
Li, WC
Yip, SP 
Huang, CL 
Issue Date: Aug-2021
Source: Frontiers in cell and developmental biology, Aug. 2021, v. 9, 643043
Abstract: Recent research has focused on the mechanisms by which long non-coding RNAs (lncRNAs) modulate diverse cellular processes such as tumorigenesis. However, the functional characteristics of these non-coding elements in the genome are poorly understood at present. In this study, we have explored several mechanisms that involve the novel lncRNA and microRNA (miRNA) axis participating in modulation of drug response and the tumor microenvironment of myeloproliferative neoplasms (MPNs). We identified novel lncRNAs via mRNA sequencing that was applied to leukemic cell lines derived from BCR-ABL1-positive and JAK2-mutant MPNs under treatment with therapeutic tyrosine kinase inhibitors (TKI). The expression and sequence of novel LNC000093 were further validated in both leukemic cells and normal primary and pluripotent cells isolated from human blood, including samples from patients with chronic myelogenous leukemia (CML). Downregulation of LNC000093 was validated in TKI-resistant CML while a converse expression pattern was observed in blood cells isolated from TKI-sensitive CML cases. In addition to BCR-ABL1-positive CML cells, the driver mutation JAK2-V617F-regulated lncRNA BANCR axis was further identified in BCR-ABL1-negative MPNs. Further genome-wide validation using MPN patient specimens identified 23 unique copy number variants including the 7 differentially expressed lncRNAs from our database. The newly identified LNC000093 served as a competitive endogenous RNA for miR-675-5p and reversed the imatinib resistance in CML cells through regulating RUNX1 expression. The extrinsic function of LNC000093 in exosomal H19/miR-675-induced modulation for the microenvironment was also determined with significant effect on VEGF expression.
Keywords: Chronic myelogenous leukemia
Long non-coding RNAs
Molecular targets
Myeloproliferative neoplasms
Tyrosine kinase inhibitor
Publisher: Frontiers Research Foundation
Journal: Frontiers in cell and developmental biology 
EISSN: 2296-634X
DOI: 10.3389/fcell.2021.643043
Rights: © 2021 Wong, Luo, Chow, Meng, Adesanya, Sun, Ma, Jin, Li, Yip and Huang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY) (https://creativecommons.org/licenses/by/4.0/). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
The following publication Wong NK, Luo S, Chow EYD, Meng F, Adesanya A, Sun J, Ma HMH, Jin W, Li W-C, Yip SP and Huang C-L (2021) The Tyrosine Kinase-Driven Networks of Novel Long Non-coding RNAs and Their Molecular Targets in Myeloproliferative Neoplasms. Front. Cell Dev. Biol. 9:643043 is available at https://doi.org/10.3389/fcell.2021.643043
Appears in Collections:Journal/Magazine Article

Files in This Item:
File Description SizeFormat 
fcell-09-643043.pdf4.44 MBAdobe PDFView/Open
Open Access Information
Status open access
File Version Version of Record
Access
View full-text via PolyU eLinks SFX Query
Show full item record

Page views

1
Citations as of May 22, 2022

Google ScholarTM

Check

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.