Target intelligence / Profile preview

Imatinib-upregulated long non-coding RNA 1 (lncRNA-IUR1)

Target
lncRNA-IUR1
Molecular classification
Long non-coding RNA (lncRNA), Other
01

Overview

Imatinib-upregulated long non-coding RNA 1 (lncRNA-IUR1, also known as LOC100129203 or LNCRNA-IUR) is a long non-coding RNA located on human chromosome 11 between the purinergic receptor P2Y2 and FCH and double SH3 domains 2 genes. It is classified as a non-coding RNA, confirmed to lack protein-coding potential, and is found in both cytoplasm and nucleus of leukemic cells. lncRNA-IUR1 is expressed at very low levels in Bcr-Abl-positive chronic myeloid leukemia cells but is strongly upregulated following treatment with imatinib. Functionally, lncRNA-IUR1 acts as a negative regulator of Bcr-Abl-induced leukemia by suppressing STAT5-mediated GATA3 expression, reducing leukemic cell survival, and promoting apoptosis. Loss of lncRNA-IUR1 expression facilitates tumor cell survival and leukemia progression in vitro and in vivo, suggesting its role as a tumor suppressor lncRNA in the context of hematological malignancies. While not a classic therapeutic target such as a receptor or enzyme, lncRNA-IUR1 has potential utility as a molecular biomarker for imatinib response, and manipulating its expression could represent a novel therapeutic strategy for CML and related disorders.

Other names
lncRNA-IUR1lncRNA imatinib upregulatedLOC100129203LNCRNA-IUR
02

Mechanism of action

Not a drug target; its upregulation by imatinib negatively regulates leukemia cell survival via suppression of the STAT5/GATA3 pathway

03

Biological functions

Negative regulation of Bcr-Abl-induced tumorigenesisRegulation of STAT5-mediated GATA3 expressionApoptosisCell survival
04

Disease associations

CancerChronic myeloid leukemia (CML)Hematological malignancies
05

Safety considerations

None specifically reported for this lncRNA. Challenges could include low endogenous expression and specificity of modulation
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Interacting drugs

07

Biomarkers

lncRNA-IUR1 expression level as a biomarker for response to imatinib in Bcr-Abl-positive leukemias

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