Highly Sensitive Real-Time Monitoring of Adenosine Receptor Activities in Nonsmall Cell Lung Cancer Cells Using Carbon Nanotube Field-Effect Transistors

Authors
Choi, YoonjiJeong, Jin-YoungHong, Seunghun
Issue Date
2024-01
Publisher
American Chemical Society
Citation
ACS Applied Materials & Interfaces, v.16, no.2, pp.2101 - 2109
Abstract
Adenosine metabolism through adenosine receptors plays a critical role in lung cancer biology. Although recent studies showed the potential of targeting adenosine receptors as drug targets for lung cancer treatment, conventional methods for investigating receptor activities often suffer from various drawbacks, including low sensitivity and slow analysis speed. In this study, adenosine receptor activities in nonsmall cell lung cancer (NSCLC) cells were monitored in real time with high sensitivity through a carbon nanotube field-effect transistor (CNT-FET). In this method, we hybridized a CNT-FET with NSCLC cells expressing A(2A) and A(2B) adenosine receptors to construct a hybrid platform. This platform could detect adenosine, an endogenous ligand of adenosine receptors, down to 1 fM in real time and sensitively discriminate adenosine among other nucleosides. Furthermore, we could also utilize the platform to detect adenosine in complicated environments, such as human serum. Notably, our hybrid platform allowed us to monitor pharmacological effects between adenosine and other drugs, including dipyridamole and theophylline, even in human serum samples. These results indicate that the NSCLC cell-hybridized CNT-FET can be a practical tool for biomedical applications, such as the evaluation and screening of drug-candidate substances.
Keywords
LABEL-FREE DETECTION; TASTE RECEPTOR; DIPYRIDAMOLE; SPECTROSCOPY; FIBRONECTIN; MOLECULES; APTAMER; BINDING; CALU-3; nonsmall cell lung cancer cell; adenosine receptor; adenosine; pharmacology; carbon nanotube field-effect transistor
ISSN
1944-8244
URI
https://pubs.kist.re.kr/handle/201004/149723
DOI
10.1021/acsami.3c14492
Appears in Collections:
KIST Article > 2024
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