Target intelligence / Profile preview

Low Expression Noncoding RNA in Gastric Adenocarcinoma (LENGA)

Target
LENGA
Molecular classification
Long noncoding RNA (lncRNA), Other
01

Overview

LENGA, also known as Low Expression Noncoding RNA in Gastric Adenocarcinoma (RRAGC Divergent Transcript, RRAGC-DT), is a long noncoding RNA found to be significantly downregulated in gastric cancer tissues compared with adjacent normal tissue. Its low expression is associated with more aggressive tumor behavior and shorter patient survival. Overexpression of LENGA suppresses gastric cancer cell proliferation and metastasis both in vitro and in vivo. Mechanistically, LENGA acts as an RNA scaffold facilitating the interaction between BRD7 and TP53, enhancing the transcriptional activation of p53 pathway genes including CDKN1A, which in turn suppresses tumorigenic processes. Its function as a tumor suppressor and its downregulation in gastric cancer make it a promising prognostic biomarker and a potential, though as yet unproven, focus for therapeutic development[1][2][3].

Other names
LENGALow Expression Noncoding RNA in Gastric AdenocarcinomaRRAGC Divergent TranscriptRRAGC-DT
02

Mechanism of action

Not applicable. No approved or experimental drugs act on this molecule currently.

03

Biological functions

Tumor suppressionRegulator of p53 pathway signaling by scaffolding interactions between BRD7 (Bromodomain-containing protein 7) and TP53 (p53), leading to transcriptional regulation of genes such as CDKN1A and PCDH7Negative regulator of cell proliferation, migration, and metastasis in gastric cancer
04

Disease associations

Cancer (specifically gastric adenocarcinoma/gastric cancer)
05

Safety considerations

None known. As LENGA is not a druggable protein and has no approved targeting agents, established safety concerns are not applicable. Potential risks of modulating lncRNAs, if targeted in the future, would require further study.
06

Biomarkers

LENGA expression is a potential prognostic biomarker for gastric cancer; lower expression correlates with poorer prognosis and more aggressive clinical features

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