Presence of an EML4-ALK gene fusion detected by microfluidic chip DNA hybridization
Author(s) -
Montek Boparai,
Christopher Oberc,
Paul C. H. Li
Publication year - 2021
Publication title -
bioscience biotechnology and biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.509
H-Index - 116
eISSN - 1347-6947
pISSN - 0916-8451
DOI - 10.1093/bbb/zbaa043
Subject(s) - biochip , fusion gene , oligonucleotide , oncogene proteins , oncogene , dna , microbiology and biotechnology , lung cancer , cancer research , fusion , biology , gene , chemistry , medicine , genetics , pathology , regulation of gene expression , cell cycle , linguistics , philosophy
Non-small cell lung cancer (NSCLC) accounts for ∼80-85% of all lung cancer cases, and the EML4-ALK fusion oncogene is a well-known contributor to NSCLC cases. Expensive methods such as FISH, IHC, and NGS have been used to detect the EML4-ALK fusion oncogene. Here, a cost-effective and facile method of detecting and differentiating an EML4-ALK fusion oncogene from the wild-type gene has been accomplished by DNA hybridization using the microfluidic biochip. First, oligonucleotide probes were confirmed for successful detection of immobilized sense strands. Second, capture of the sense PCR product strands (fusion and WT) and their subsequent detection and differentiation were accomplished. Our proof-of-concept study shows the ability to detect 1% fusion products, among WT ones.
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