Literature DB >> 30328369

Vitamin B12-conjugated sericin micelles for targeting CD320-overexpressed gastric cancer and reversing drug resistance.

Weihong Guo1, Lizhi Deng2, Zhaoyu Chen1, Zhian Chen1, Jiang Yu1, Hao Liu1, Tuanjie Li1, Tian Lin1, Hao Chen1, Mingli Zhao1, Liming Zhang2, Guoxin Li1, Yanfeng Hu1.   

Abstract

AIM: Our previous research has introduced sericin micelles to reverse drug resistance. However, these micelles could not selectively bind to gastric cancer (GC) cells. We developed vitamin B12 (VB12) conjugated sericin micelles for targeted GC therapy. MATERIALS &
METHODS: We used VB12, sericin, synthetic poly(γ-benzyl-L-glutamate) (PBLG) and paclitaxel (PTX) to develop VB12-conjugated and PTX-loaded micelles (VB12-sericin-PBLG-PTX). Then we explored their physicochemical properties, cellular uptake and antitumor mechanism.
RESULTS: VB12-sericin-PBLG-PTX micelles were proved to be of appropriate particle size, have good dispersion and are bio-safe. Following transcobalamin II (CD320)-receptor-mediated endocytosis, these swallowed micelles with GC-targeting and enhanced cellular uptake abilities, alter mitochondrial transmembrane potential/apoptosis pathway and reverse drug resistance.
CONCLUSION: VB12-sericin-PBLG-PTX micelles are promising materials for GC-targeted clinical applications.

Entities:  

Keywords:  drug resistance; gastric cancer; micelle; sericin; vitamin B12

Mesh:

Substances:

Year:  2018        PMID: 30328369     DOI: 10.2217/nnm-2018-0321

Source DB:  PubMed          Journal:  Nanomedicine (Lond)        ISSN: 1743-5889            Impact factor:   5.307


  9 in total

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9.  Biodegradable hollow mesoporous organosilica nanotheranostics (HMON) for multi-mode imaging and mild photo-therapeutic-induced mitochondrial damage on gastric cancer.

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  9 in total

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