Development of a DNA Aptamer against Multidrug-Resistant Hepatocellular Carcinoma for In Vivo Imaging.
Lin ZhangLingli ZhouHui ZhangYibin ZhangLing LiTiantian XieYinglei ChenXiaodong LiNeng LingJing DaiXing SunMridul RoyJinfeng ZhaoTianhuan PengMao YePublished in: ACS applied materials & interfaces (2021)
Hepatocellular carcinoma (HCC) is a type of cancer that has high rates of recurrence and mortality. One of the most important factors that lead to treatment failure of HCC is the acquisition of multidrug resistance (MDR). Development of specific ligands for multidrug-resistant HCC will provide useful molecular tools for precise diagnosis and targeted theranostics. Herein, a multidrug-resistant HCC cell (HepG2/MDR)-specific aptamer was developed through Cell-SELEX (systematic evolution of ligands by exponential enrichment) technology. With dissociation constants lying in the nanomolar range, the molecularly designed PS-ZL-7c aptamer showed great selectivity to drug-resistant cancer cells. The in vivo imaging results illustrated that the PS-ZL-7c specifically accumulated in the drug-resistant tumors but not in drug-sensitive tumors and normal tissues, indicating that the PS-ZL-7c aptamer possessed excellent potential as a targeting ligand for precise diagnosis and target theranostics of multidrug-resistant HCC.
Keyphrases
- multidrug resistant
- drug resistant
- acinetobacter baumannii
- gram negative
- gold nanoparticles
- sensitive detection
- klebsiella pneumoniae
- high resolution
- single cell
- magnetic nanoparticles
- label free
- cell therapy
- gene expression
- cancer therapy
- papillary thyroid
- single molecule
- type diabetes
- fluorescence imaging
- escherichia coli
- mesenchymal stem cells
- cell free
- coronary artery disease
- cystic fibrosis
- cardiovascular events
- young adults
- bone marrow
- pseudomonas aeruginosa
- mass spectrometry
- adverse drug
- climate change
- photodynamic therapy