Target intelligence / Profile preview

MicroRNA 1324 (miR-1324)

Target
miR-1324
Molecular classification
microRNA, non-coding RNA, miRNA class
01

Overview

MicroRNA 1324 is a member of the microRNA class of short (20–24 nucleotide) non-coding RNAs, which regulate gene expression in multicellular eukaryotes at the post-transcriptional level[1][6]. MIR1324 is processed from a precursor transcript through the typical Drosha/Dicer pathway. The mature miR-1324 is incorporated into the RNA-induced silencing complex (RISC), enabling recognition of target mRNAs via imperfect base pairing, most commonly resulting in translational inhibition or mRNA destabilization[1][6]. In the context of human disease, MIR1324 has been reported to inhibit cell proliferation and invasiveness in gastric cancer by targeting MECP2[1]. It is also associated with Hirschsprung Disease 1[1]. While microRNAs are increasingly investigated as therapeutic and diagnostic targets, MIR1324 itself does not have recognized direct drug interactions, validated biomarkers, or noted safety concerns. The broader family plays important regulatory roles in cell differentiation, proliferation, apoptosis, and disease biology[5][6].

Other names
hsa-mir-1324MIRN1324MIR1324GC00U923171
02

Mechanism of action

Not applicable (no direct drugs targeting MIR1324; miRNA-targeting therapies generally seek to modulate miRNA activity by mimic or inhibitor molecules, affecting gene silencing)

03

Biological functions

Post-transcriptional regulation of gene expressionInhibition of mRNA translationDestabilization of target mRNAsPotential inhibition of cell proliferation and invasiveness (demonstrated in gastric cancer by targeting the gene MECP2)General miRNA functions include cell differentiation, cell proliferation, apoptosis, and various roles in development and homeostasis
04

Disease associations

Linked to Hirschsprung Disease 1Functional data indicate a potential tumor-suppressive role in gastric cancerMicroRNA dysfunction broadly implicated in various human diseases, including cancer, developmental disorders, and others
05

Safety considerations

Not established (no safety issues specifically attributed to MIR1324; therapeutic modulation of microRNAs can present off-target effects and complex biological consequences)
06

Interacting drugs

None known (no approved or investigational drugs directly target MIR1324; drug development mostly targets more common miRNA or their pathways)
07

Biomarkers

None established for MIR1324; microRNAs are often explored as biomarkers for patient selection or disease monitoring, but MIR1324 is not recognized as a standard biomarker

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