Drug intelligence / Profile preview

miR-93 lentiviral vector

Development stage
Preclinical
Lead developer
Chinese Academy of Medical Sciences
Modality
Gene Therapies, RNA Therapeutics → Nucleic Acid Therapeutics
Administration
Intratumoral, Intravenous, Intraperitoneal
01

Overview

miR-93 lentiviral vector is an experimental gene therapy construct designed to overexpress microRNA-93 (miR-93). In the context of hematological malignancies such as Acute Myeloid Leukemia (AML), miR-93 is recognized as a member of the miR-106b-25 cluster that contributes to chemoresistance and accelerated cell growth. The vector functions by delivering the miR-93 sequence into target cells, where the resulting miRNA overexpression leads to the downregulation of pro-apoptotic targets, specifically Tumor protein p73 (TP73) and Caspase-7. This suppression of apoptotic pathways promotes leukemic cell survival and resistance to treatments such as doxorubicin and BCL-2 inhibitors. It is primarily utilized as a research tool in preclinical models to elucidate the mechanisms of drug resistance and oncogenesis.

Other names
lentiviral miR-93miR-93-expressing lentiviral vectormiR93-expressing lentiviral vectormiR 93-expressing lentiviral vector
02

Targets

CDKN1A (Cyclin-dependent kinase inhibitor 1A)CASP7 (Caspase-7)Tumor protein p73 mRNASerine/threonine kinase 11 messenger RNA 3′ untranslated regionTumor protein p53-inducible nuclear protein 1 mRNA 3' untranslated regionPTEN (Phosphatase and tensin homolog deleted on chromosome ten)

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