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University of Illinois at Urbana-Champaign

Controlled metabolic cell labeling and bioorthogonal click chemistry for cancer targeting

Abstract

dc:description

The aim of my Ph.D. research is to develop a new, transformative cancer targeted therapy via the combination of unnatural sugar-mediated controlled metabolic cell labeling and bioorthogonal Click chemistry. By controlling the metabolic glycoengineering processes of unnatural sugars via rational chemistry designs, I was able to design a library of trigger-activatable sugar precursors that can label cell surface with chemical groups (e.g., azides) only in the presence of either exogenous triggers (ultraviolet (UV)) or endogenous triggers (H2O2, tumor hypoxia, NAD(P)H dehydrogenase quinone 1 (NQO1), and histone deacetylase (HDAC)/cathepsin L (CTSL)). Among them, HDAC/CTSL-responsive acetylated azidomannose (DCL-AAM) mediated excellent cancer-specific labeling in vitro and in vivo, which enhanced tumor accumulation of dibenzocyclooctyne (DBCO)-drug conjugates via efficient Click Chemistry between azides and DBCO and consequently exerted robust anticancer activities against LS174T colon cancer, MDA-MB-231 triple-negative breast cancer, and 4T1 metastatic breast cancer in murine models. DCL-AAM coupled with DBCO-drug conjugates, a new cancer targeted therapy which I name as Active Tissue Targeting via Anchored ClicK Chemistry (ATTACK), is essentially the small molecule version of antibody/antigen targeting technology and shows multiple advantages. Apart from the efforts in rational chemical designs of azido-sugars, I also developed sugar-loaded micelles and microbubbles for tumor labeling and targeting, in an effort to fully evaluate the advantages of Click chemistry-based cancer targeting strategy. Last but not least, I demonstrated that different types of unnatural sugars (e.g., azido-mannose and azido-galactose) have distinct labeling efficiencies in varying cancer types and that the use of reversible chemistries can impart the recyclability of cell-surface chemical receptors.

Degree

thesis:*
Name thesis:degree_name
Ph.D.
Level thesis:degree_level
Dissertation
Discipline thesis:degree_discipline
Materials Science & Engr
Grantor
University of Illinois at Urbana-Champaign
Year dc:date
2016

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Wang, Hua
Contributors dc:contributor
  • Cheng, Jianjun
  • Kilian, Kristopher A.
  • Lu, Yi
  • Leal, Cecilia
  • O'Brien, William D.

Subjects

dc:subject × 8

Rights

dc:rights
Statement dc:rights
  • Copyright 2016 Hua Wang
Language dc:language
en

Identifiers

dc:identifier.*
Handle dc:identifier
http://hdl.handle.net/2142/90943
OAI identifier oai:identifier
oai:www.ideals.illinois.edu:2142/90943

Chain of custody

source
Harvested from
University of Illinois - Urbana-Champaign
Base URL
www.ideals.illinois.edu/oai-pmh
Last updated
2026-07-22
Source record
OAI-PMH GetRecord
citation

Wang, Hua. Controlled metabolic cell labeling and bioorthogonal click chemistry for cancer targeting. Dissertation thesis, University of Illinois at Urbana-Champaign, 2016. http://hdl.handle.net/2142/90943