Abstract
This study is aimed at evaluating the potential of a biochip assay to sensitively detect KRAS mutation in DNA from non-small cell lung cancer (NSCLC) tissue samples. The assay covers 10 mutations in codons 12 and 13 of the KRAS gene, and is based on mutant-enriched PCR followed by reverse-hybridization of biotinylated amplification products to an array of sequence-specific probes immobilized on the tip of a rectangular plastic stick (biochip). Biochip hybridization identified 17 (21%) samples to carry a KRAS mutation of which 16 (33%) were adenocarcinomas and 1 (3%) was a squamous cell carcinoma. All mutations were confirmed by DNA sequencing. Using 10 ng of starting DNA, the biochip assay demonstrated a detection limit of 1% mutant sequence in a background of wild-type DNA. Our results suggest that the biochip assay is a sensitive alternative to protocols currently in use for KRAS mutation testing on limited quantity samples. © 2011 by the authors; licensee MDPI, Basel, Switzerland.
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Kriegshäuser, G., Fabjani, G., Ziegler, B., Zöchbauer-Müller, S., End, A., & Zeillinger, R. (2011). Biochip-based detection of KRAS mutation in non-small cell lung cancer. International Journal of Molecular Sciences, 12(12), 8530–8538. https://doi.org/10.3390/ijms12128530
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