Drug intelligence / Profile preview

PCSK9-LYTAC

Development stage
Unknown
Lead developer
University of Chinese Academy of Sciences
Modality
Small Interfering RNA (siRNA) → Small RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, MicroRNA (miRNA) → Small RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, Antisense Oligonucleotides (ASOs) → Long RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, Antisense DNA → DNA Therapeutics → Nucleic Acid Therapeutics
01

Overview

PCSK9-LYTAC: sourced facts only. name: "Here, we report the development of a bispecific DNA aptamer-based lysosome-targeting chimera (PCSK9-LYTAC) that promotes extracellular degradation of PCSK9 via IGFIIR-mediated lysosomal trafficking." [PMID:41707385]; target: "Here, we report the development of a bispecific DNA aptamer-based lysosome-targeting chimera (PCSK9-LYTAC) that promotes extracellular degradation of PCSK9 via IGFIIR-mediated lysosomal trafficking." [PMID:41707385]; developer: "School of Chemical Sciences, University of Chinese Academy of Sciences, Beijing 100049, PR China; Central Laboratory, Shanxi Province Cancer Hospital/Shanxi Hospital Affiliated to Cancer Hospital, Chinese Academy of Medical Sciences/Cancer Hospital Affiliated to Shanxi Medical University, Taiyuan 030001, Shanxi, China." [PMID:41707385]; modality: "Here, we report the development of a bispecific DNA aptamer-based lysosome-targeting chimera (PCSK9-LYTAC) that promotes extracellular degradation of PCSK9 via IGFIIR-mediated lysosomal trafficking." [PMID:41707385]; stage: "In HepG2 cells, PCSK9-LYTAC efficiently undergoes lysosomal localization and significantly restores LDL uptake (∼22% recovery), outperforming the corresponding monovalent PCSK9 aptamer." [PMID:41707385]

02

Targets

PCSK9 (Proprotein convertase subtilisin/kexin type 9)

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