4.3 Article

Identification of a Lung Cancer Biomarker Using a Cancer Cell Line and Screening of Olfactory Receptors for Biomarker Detection

期刊

BIOTECHNOLOGY AND BIOPROCESS ENGINEERING
卷 26, 期 1, 页码 55-62

出版社

KOREAN SOC BIOTECHNOLOGY & BIOENGINEERING
DOI: 10.1007/s12257-020-0132-4

关键词

volatile organic compound; lung cancer; human olfactory receptor; solid-phase microextraction; GC; MS

资金

  1. Basic Science Research Program through the National Research Foundation of Korea (NRF) - Ministry of Education, Science and Technology [2015025739]
  2. National Research Foundation of Korea (NRF) - Ministry of Science and ICT (MSIT) of Korea [2018R1A2B3004498]

向作者/读者索取更多资源

This study identified a potential lung cancer biomarker, 2-ethyl-1-hexanol, through an in vitro cancer system; additionally, the olfactory receptor 4D11P was identified as the receptor for this specific marker through screening human olfactory receptor libraries and expressed heterologously in nanovesicles.
Several studies investigated the development of a non-invasive and early diagnostic method for cancer. Recently, the volatile organic compounds (VOCs) exhaled from cancer patients have been shown to act as a potential biomarker for cancer. However, the gas profile of breath is highly variable and not conducive to identification of biomarkers accurately. Accordingly, we identified a cancer-specific VOC as a biomarker using an in vitro cancer system in order to exclude the variables from patient condition. VOCs were collected from the headspace gas of lung cancer cell line (SK-MES) and normal lung cell line (MRC-5), followed by analysis using solid-phase microextraction (SPME)-GC/MS. As a result, 2-ethyl-1-hexanol was detected from headspace gas of SK-MES and decided as a potential biomarker for lung cancer. By screening human olfactory receptor libraries to detect a lung cancer biomarker, human olfactory receptor 4D11P (hOR4D11P) was identified as a receptor specific for 2-ethyl-1-hexanol and expressed heterologously in HEK293 cells. Additionally, we generated nanovesicles containing hOR4D11P from HEK293 cells and confirmed the expression and functionality of hOR4D11P in nanovesicles.

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