Target intelligence / Profile preview

Long intergenic non-protein coding RNA 173 (LINC00173) (LINC00173)

Target
LINC00173
Molecular classification
Long non-coding RNA (lncRNA), Long intergenic non-protein coding RNA
01

Overview

Long intergenic non-protein coding RNA 173 (LINC00173) is a long non-coding RNA transcript (~543 nucleotides, chromosome 12q24.22), with no known protein-coding capacity[1]. It has several transcript variants and is found in both nuclear and cytoplasmic compartments, influencing gene expression at both the transcriptional and post-transcriptional levels. LINC00173 is aberrantly expressed in at least eleven human cancers, where it often functions as a competitive endogenous RNA (“ceRNA” or miRNA sponge), thereby regulating downstream target genes involved in cell proliferation, migration, invasion, apoptosis, and resistance to chemotherapy. Its dysregulation has been implicated in cancer development, progression, and chemoresistance, making it a novel candidate biomarker and a potential therapeutic target, although it is not a receptor, enzyme, or conventional drug target[1][3].

Other names
NCRNA00173LINC00173
02

Mechanism of action

Regulation of downstream gene expression through miRNA “sponging” (e.g., binds miR-765, miR-218, miR-182-5p, miR-641, miR-338-3p, etc.) Modulates chemoresistance mechanisms and influences cell fate via regulation of oncogenes and tumor suppressors downstream of these miRNAs (e.g., PLP2, Etk, NUTF2, VEGFA, RAB14, Rab25, FBXW7, AGER/NF-κB pathway, SPHK1, MGAT1)

03

Biological functions

Regulation of cell proliferationRegulation of cell migrationRegulation of cell invasionApoptosisRegulation of chemoresistanceTranscriptional and post-transcriptional gene regulation (as competing endogenous RNA or miRNA sponge)
04

Disease associations

Cancer (multiple types, including lung cancer, glioma, colorectal cancer, breast cancer, esophageal squamous cell carcinoma, gastric cancer, hepatocellular carcinoma, prostate cancer, Wilms tumor, and acute myeloid leukemia)Chemoresistance in tumorsNon-tumor diseases (e.g., hypertrophic scar, polycystic ovarian syndrome)
05

Safety considerations

As an RNA target, direct therapeutic modulation (e.g., siRNA, antisense oligonucleotides) of LINC00173 remains experimentalPossible challenges include off-target effectsPossible challenges include tissue specificityPossible challenges include delivery issues
06

Biomarkers

Aberrant LINC00173 expression has been reported as a potential biomarker for cancer diagnosis and prognosis, particularly in relation to its expression level in certain tumor types and chemoresistance profiles

Beyond the preview

Go deeper on Long intergenic non-protein coding RNA 173 (LINC00173) (LINC00173).

Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.

Drug pipeline

Full profile access

Explore the programs pursuing this target and their development progress.

  • Drug candidates
  • Developers
  • Development stage

Clinical trials

Full profile access

Follow the clinical studies evaluating therapies directed at this target.

  • Trial design
  • Status
  • Readouts

Competitive landscape

Full profile access

Compare approaches across drug candidates, modalities, and indications.

  • Programs
  • Modalities
  • Indications

Literature & evidence

Full profile access

Investigate the research and source evidence behind target biology and development.

  • Publications
  • Sources
  • Analysis

Patents

Full profile access

Explore patent activity around therapies and technologies addressing this target.

  • Patents
  • Assignees
  • Technologies

Research & analysis

Full profile access

Connect target biology, drug development, and emerging evidence in your research.

  • Biology
  • Development news
  • Analysis

Bring the full picture into focus.

See how Gosset can support your research on Long intergenic non-protein coding RNA 173 (LINC00173) (LINC00173).

Explore the full profile

Gosset Free

Get started with Gosset.

Enter your work email and we’ll be in touch with next steps.

Work email preferred.

Book a call