Drug intelligence / Profile preview

Lectin-Dox

Development stage
Preclinical
Lead developer
National Institute of Advanced Industrial Science and Technology
Modality
Small Molecules, Recombinant Proteins and Enzymes, Nanoparticles → Drug Delivery Systems
Administration
Intravenous
01

Overview

**Lectin-Dox** is an investigational glycan-targeted liposomal doxorubicin formulation developed for pancreatic cancer. It consists of doxorubicin encapsulated in a PEGylated liposome whose surface is modified with the recombinant lectin rBC2LCN. rBC2LCN binds fucosylated cell-surface glycans, including H type-3 glycan motifs enriched on susceptible pancreatic cancer cells, to promote selective tumor-cell binding and uptake; intracellular doxorubicin then produces cytotoxicity through DNA intercalation and topoisomerase II inhibition. In preclinical Capan-1 pancreatic cancer models with high rBC2LCN binding, Lectin-Dox showed greater cellular uptake and a trend toward greater antitumor activity than non-lectin-modified liposomal doxorubicin. ([aacrjournals.org](https://aacrjournals.org/cancerres/article/79/13_Supplement/2152/634295/Abstract-2152-A-novel-glycan-targeting-cancer))

02

Targets

TOP2A (DNA topoisomerase II)Fucosylated cell-surface glycansDNABG-H3 (Fucosylated H type-3 glycan)

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