Target intelligence / Profile preview

microRNA 449a (miR-449a)

Target
miR-449a
Molecular classification
microRNA, Non-coding RNA, Gene regulator (post-transcriptional)
01

Overview

microRNA 449a (miR-449a) is a small, non-coding RNA molecule belonging to the microRNA family, encoded in the human genome within the second intron of the CDC20B gene[3]. It acts post-transcriptionally by binding to the 3’ untranslated regions (3’UTRs) of target mRNAs, leading to gene silencing, mainly via mRNA degradation or translational repression. miR-449a functions as a tumor suppressor in several cancers including neuroblastoma, non-small cell lung cancer, prostate cancer, and breast cancer, where its expression is often downregulated in tumor tissues compared to normal tissues[1][2][4][5]. Functionally, miR-449a inhibits tumor cell proliferation, induces G1 phase cell cycle arrest, promotes apoptosis, and enhances cellular differentiation, largely by repressing oncogenic and cell cycle–related genes such as CDK6, LEF1, c-MET, NOTCH1, BCL2, and others. Loss or downregulation of miR-449a is consistently associated with increased malignancy, metastatic potential, and poorer clinical outcomes[1][2][4]. While miR-449a is not currently the direct target of any approved drugs, its expression profile may serve as a biomarker for diagnosis, prognosis, or therapeutic response in certain cancers[1][2][4][5].

Other names
hsa-mir-449hsa-mir-449aMIRN449MIRN449AMIR449Amir-449amicroRNA 449mir-449
02

Mechanism of action

Not applicable; miR-449a acts as an endogenous tumor suppressor by downregulating specific mRNA targets[1][2][4].

03

Biological functions

Cell cycle regulationInduction of cell differentiationInduction of apoptosisInhibition of cell proliferationRegulation of gene expressionCellular senescence
04

Disease associations

Cancer (including neuroblastoma, non-small cell lung cancer, prostate cancer, breast cancer)Tumor suppression
05

Safety considerations

Challenges for direct therapeutic targeting include delivery, specificity, and risks of off-target effects[1].
06

Interacting drugs

None established; no drug directly targets miR-449a at this time[1][2][5].
07

Biomarkers

Downregulated expression in several tumor types (breast, lung, prostate, neuroblastoma) is associated with cancer progression and poor prognosis[1][2][4][5].

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