2010肿瘤研究与临床Requires access

Detection of EGFR genemutations in patients with non-small cell lung cancer by denaturing high performanceliquid chromatography technology

Dan Cai

Open publisher page 0 citations

Abstract

:Objective To investigatethe advantages of detection for EGFR gene mutations by denaturing high performance liquidchromatography (DHPLC) technology. Methods DHPLC was used to detect EGFR gene mutations atexon 19 and 21 in 49 cases of non-small cell lung cancer (NSCLC) patients,and the directDNA sequencing was used to verify the accuracy of DHPLC detection. Results EGFR genemutation was identified from 13 of 49 cases by DHPLC,including deletion mutation at exon19 in 10 cases (76.92 %) and alternative mutations at exon 21 in 3 cases (23.08 %).Mutation results of DHPLC was consistent with DNA direct sequencing. The results of thedirect DNA sequencing were the same as those of DHPLC. The sensitivity of mutation test byDHPLC was 100 %. Conclusion DHPLC technology can be used for large scale screening of EGFRgene mutation with rapid and accuracy.

About this research paper

What this paper is about

:Objective To investigatethe advantages of detection for EGFR gene mutations by denaturing high performance liquidchromatography (DHPLC) technology. Methods DHPLC was used to detect EGFR gene mutations atexon 19 and 21 in 49 cases of non-small cell lung cancer (NSCLC) patients,and the directDNA sequencing was used to verify the accuracy of DHPLC detection. Results EGFR genemutation was identified from 13 of 49 cases by DHPLC,including deletion mutation at exon19 in 10 cases (76.92 %) and alternative mutations at exon 21 in 3 cases (23.08 %).Mutation results of DHPLC was consistent with DNA direct sequencing. The results of thedirect DNA sequencing were the same as those of DHPLC. The sensitivity of mutation test byDHPLC was 100 %. Conclusion DHPLC technology can be used for large scale screening of EGFRgene mutation with rapid and accuracy.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

:Objective To investigatethe advantages of detection for EGFR gene mutations by denaturing high performance liquidchromatography (DHPLC) technology. Methods DHPLC was used to detect EGFR gene mutations atexon 19 and 21 in 49 cases of non-small cell lung cancer (NSCLC) patients,and the directDNA sequencing was used to verify the accuracy of DHPLC detection. Results EGFR genemutation was identified from 13 of 49 cases by DHPLC,including deletion mutation at exon19 in 10 cases (76.92 %) and alternative mutations at exon 21 in 3 cases (23.08 %).Mutation results of DHPLC was consistent with DNA direct sequencing. The results of thedirect DNA sequencing were the same as those of DHPLC. The sensitivity of mutation test byDHPLC was 100 %. Conclusion DHPLC technology can be used for large scale screening of EGFRgene mutation with rapid and accuracy.

Key concepts: Denaturing high performance liquid chromatography, Exon, Lung cancer, Mutation, Molecular biology, DNA sequencing, Biology, Gene

Related papers

Back to paper searchBrowse research topicsOriginal source
Detection of EGFR genemutations in patients with non-small cell lung cancer by denaturing high performanceliquid chromatography technology — Research Paper | ScholarLens