Self-Assembled 2D Glycoclusters for the Targeted Delivery of Theranostic Agents to Triple-Negative Breast Cancer Cells.
Xi-Le HuQuanyu CaiJie GaoRobert A FieldGuo-Rong ChenNingyang JiaYi ZangJia LiXiao-Peng HePublished in: ACS applied materials & interfaces (2019)
Triple-negative breast cancer (TNBC) is a devastating disease worldwide, for which targeted imaging and therapeutic agents remain elusive. There has been growing awareness that carbohydrates are valuable as drug candidates and targeting agents for a variety of human diseases, including cancers that overexpress carbohydrate receptors on the cell surface. Here, we develop a two-dimensional (2D) glycocluster by means of simple, stepwise self-assembly for the targeted delivery of theranostic agents to TNBC cells that express mannose receptors (MRs) on the cell surface. Human serum albumin, which contains a variety of hydrophobic pockets capable of accommodating small molecules, was used to simultaneously encapsulate a mannose-based glycoprobe and a commercial photosensitizer (i.e., Ce6). The multicomponent "neoglycoprotein" formed was used to self-assemble with 2D MnO2, producing 2D glycoclusters, which could be selectively internalized by a TNBC cell line (MDA-MB-231) as facilitated by binding to the transmembrane MR. The intracellular degradation of the 2D MnO2 backbone by biothiols then released Ce6 for cell imaging and, subsequently, photodynamic therapy. This study provides insights into the development of carbohydrate-based materials for targeted, stimuli-responsive theranostics of TNBC.
Keyphrases
- photodynamic therapy
- cell surface
- fluorescence imaging
- cancer therapy
- breast cancer cells
- high resolution
- human serum albumin
- induced apoptosis
- endothelial cells
- cell cycle arrest
- single cell
- drug delivery
- magnetic resonance
- magnetic resonance imaging
- cell therapy
- cell death
- emergency department
- oxidative stress
- young adults
- signaling pathway
- energy transfer
- endoplasmic reticulum stress
- cell proliferation
- ionic liquid
- drug induced
- induced pluripotent stem cells
- fluorescent probe
- pi k akt