Target intelligence / Profile preview

Long intergenic non-protein coding RNA 332 (LINC00332)

Target
LINC00332
Molecular classification
Long non-coding RNA (lncRNA), non-coding RNA, RNA gene
01

Overview

Long intergenic non-protein coding RNA 332 (LINC00332) is a human long non-coding RNA (lncRNA) gene located on chromosome 13 (chr13:40181809-40195040, hg38)[7][5]. LINC00332 is transcribed but not translated into protein and is classified within the growing family of lncRNAs, which are transcripts longer than 200 nucleotides with regulatory roles in cellular function and disease[1][11]. In gastric cancer, LINC00332 acts as a tumor suppressor: its expression is significantly downregulated in cancer tissues as compared to normal, and ectopic (experimental) overexpression of LINC00332 reduces markers of epithelial–mesenchymal transition (EMT), inhibits cell proliferation, migration, and invasion, but does not promote apoptosis[2]. LINC00332 may mediate these effects through inverse regulation of matrix metalloproteinase-13 (MMP-13), and may decrease resistance to chemotherapy (cisplatin)[2][4]. It is also implicated in broader lncRNA-mediated regulatory networks, such as ceRNA (competing endogenous RNA) cross-talk, possibly via sponging microRNAs and affecting gene expression relevant to cancer biology[6][8]. Current evidence does not characterize LINC00332 as a classical druggable "target" such as a receptor, enzyme, or transporter, but rather as a regulatory RNA with disease relevance, particularly as a tumor suppressive factor in select cancers[2][4][11].

Other names
NCRNA00332non-protein coding RNA 332
02

Biological functions

Regulation of gene expressionNegative regulator of epithelial–mesenchymal transition (anti-EMT)Inhibition of cell proliferation, migration, and invasion in certain cancer cell modelsPotential involvement in ceRNA (competing endogenous RNA) networks
03

Disease associations

Cancer (notably gastric cancer, possible roles in other tumor types via general lncRNA functions)
04

Biomarkers

Potential as biomarker for gastric cancer prognosis and response to chemotherapy (cisplatin)

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