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MicroRNA 1252 (miR-1252 (also seen as miR-1252-5p when referring to mature strand))

Target
miR-1252 (also seen as miR-1252-5p when referring to mature strand)
Molecular classification
MicroRNA, Non-coding RNA, Small regulatory RNA, Other
01

Overview

MicroRNA 1252 is a small, non-coding RNA (approximately 22 nucleotides) involved in post-transcriptional gene silencing via binding to target mRNAs, leading to their degradation or translational repression[5]. In humans, it is encoded at chromosome 12q21.2 and is mainly studied in its mature form, miR-1252-5p. It has been found to act as a tumor suppressor in pancreatic adenocarcinoma by inhibiting cell migration, invasion, proliferation, and epithelial-mesenchymal transition—largely through direct targeting and downregulation of genes such as NEDD9 and HPSE[1][3]. In multiple myeloma, higher miR-1252-5p levels sensitize cells to the chemotherapeutic agent bortezomib by repressing heparanase (HPSE) expression. The molecule participates in various cancer-related pathways and is part of the broader family of microRNAs, which are deeply involved in fine-tuning gene networks through Argonaute protein-mediated mechanisms[4][5]. There are currently no approved drugs that directly target microRNA 1252 for therapeutic purposes, but synthetic mimics or inhibitors are under investigation for their potential in cancer therapy[3].

Other names
hsa-miR-1252hsa-mir-1252MIR1252MIRN1252microRNA-1252-5pmiR-1252-5p
02

Mechanism of action

Functions as a gene silencer by binding to complementary sequences in target mRNAs, leading to mRNA degradation or inhibition of translation. Sensitizes cells to bortezomib by downregulating expression of heparanase (HPSE).

03

Biological functions

Post-transcriptional gene regulationRegulation of cell proliferationRegulation of apoptosisInhibition of cell migration and invasionTumor suppression
04

Disease associations

Cancer (e.g., pancreatic adenocarcinoma, non-small cell lung cancer, head and neck cancers, multiple myeloma)
05

Safety considerations

Potential off-target effects if modulated therapeuticallyUnintended modulation of gene networks due to pleiotropic targeting (typical of microRNAs)
06

Interacting drugs

Bortezomib (BTZ) (sensitization via targeting heparanase/HPSE)
07

Biomarkers

miR-1252-5p expression (proposed as a marker for tumor prognosis and therapy response in certain cancers)

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