Target intelligence / Profile preview

MicroRNA 1204 (miR-1204)

Target
miR-1204
Molecular classification
microRNA, Non-coding RNA, Epigenetic regulator
01

Overview

MicroRNA 1204 (miR-1204) is a short non-coding RNA molecule found in the human genome within the PVT1 region at chromosome 8q24. It is involved in post-transcriptional regulation of gene expression by guiding the RNA-induced silencing complex (RISC) to specific messenger RNAs, resulting in their translational repression or degradation[3]. miR-1204 is overexpressed in several types of cancer, including breast, ovarian, and non-small-cell lung cancer, where it promotes cell proliferation, reduces cell cycle arrest, and inhibits tumor suppressor gene expression such as PITX1[1][2][4]. Inhibition of miR-1204 using antisense oligonucleotides can reduce tumor growth and induce apoptosis in PVT1-amplified cancers[2]. Elevated miR-1204 levels are associated with poor prognosis and more aggressive disease phenotypes, making it both a biomarker and a potential therapeutic target in oncology[1][2][4].

Other names
MIR1204hsa-mir-1204hsa-miR-1204microRNA-1204
02

Mechanism of action

Antisense oligonucleotides (antagomirs) inhibit miR-1204 activity, leading to reduced cell proliferation and increased apoptosis in cancer cells[2].

03

Biological functions

Post-transcriptional regulation of gene expressionRegulation of cell proliferationRegulation of cell cyclePromotion of cell survivalContribution to cell death avoidance
04

Disease associations

CancerBreast cancerOvarian cancerNon-small-cell lung cancerTumor progression
05

Safety considerations

Potential for adverse effects if targeted due to its involvement in essential cellular processes such as proliferation and survival; on-target effects in non-cancerous tissues may be a concern (inferred based on biology of microRNAs)[3][6].
06

Biomarkers

High miR-1204 expression as a negative prognostic biomarker in non-small-cell lung cancer[1][4].High miR-1204 expression correlates with increased tumor size, lymph node metastasis, and advanced TNM stage[1][4].

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