Target intelligence / Profile preview

Prostate cancer-associated transcript 1 (PCAT1)

Target
PCAT1
Molecular classification
Long non-coding RNA (lncRNA), Other (does not code for protein; not a receptor, enzyme, etc.)
01

Overview

Prostate cancer-associated transcript 1 (PCAT1) is a long non-coding RNA (~1900–2000 nt) located at chromosome 8q24, identified via RNA sequencing in prostate tumors, and found to be upregulated in advanced forms and metastases across several cancers. PCAT1 acts primarily as a transcriptional repressor, notably silencing the tumor suppressor BRCA2 and thereby impairing homologous recombination DNA repair, which increases cellular sensitivity to PARP1 inhibitors. It also promotes cancer cell proliferation by upregulating the MYC oncogene and acts as a microRNA sponge, binding miR-326 and miR-122, thus deregulating multiple cell growth pathways. PCAT1 expression is linked to poorer prognosis, higher metastatic potential, and advanced tumor stages; its detection in tissue and serum is being explored as a non-invasive biomarker. Knockdown or silencing of PCAT1 in experimental models suppresses tumor growth and increases chemosensitivity, supporting its potential as a therapeutic target.

Other names
PCAT-1PCA1PiHLLoc105375751Prostate cancer associated transcript 1 (non-protein coding)Prostate cancer-associated lncRNA transcript 1
02

Mechanism of action

Synthetic interference/antisense or shRNA (experimental; knockdown of PCAT1 reduces cancer cell growth and invasion); Combination therapy potential (enhances efficacy of DNA repair inhibitors and select chemotherapeutics)

03

Biological functions

Transcriptional repression (negatively regulates tumor suppressor BRCA2)Cancer cell proliferation (upregulates MYC, promotes cell cycle progression)Promotion of migration and invasion (stimulates metastatic phenotype)MicroRNA sponge (binds miRNAs such as miR-326, miR-122)Cell cycle regulation (affects cyclins and cell cycle checkpoints)Epithelial-mesenchymal transition (EMT) regulation
04

Disease associations

Cancer (prostate, non-small cell lung, esophageal squamous cell, colorectal, bladder, hepatocellular, gastric, breast, glioblastoma, multiple myeloma, osteosarcoma)
05

Safety considerations

Therapeutic specificity (lncRNAs often expressed in multiple tissues, raising potential off-target effects)Delivery challenges (RNA-targeting therapies may face issues of stability, biodistribution, and toxicity)Functional redundancy (complexity and compensation among lncRNAs can complicate therapeutic efficacy)
06

Interacting drugs

PARP1 inhibitors

2 more in the full profile.

07

Biomarkers

Serum PCAT1 levels (detectable in patient exosomes; non-invasive biomarker for ESCC and possibly other cancers)Tissue PCAT1 expression (overexpression linked to poor prognosis/progression in multiple cancers)

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