TaqMan based real time PCR assay targeting EML4-ALK fusion transcripts in NSCLC
Language English Country Ireland Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
24792336
DOI
10.1016/j.lungcan.2014.04.002
PII: S0169-5002(14)00169-X
Knihovny.cz E-resources
- Keywords
- EML4-ALK, FISH, Lung cancer, NSCLC, Real time PCR, Targeted therapy,
- MeSH
- Adenocarcinoma diagnosis genetics MeSH
- Molecular Diagnostic Techniques MeSH
- DNA Probes chemistry MeSH
- Oncogene Proteins, Fusion genetics metabolism MeSH
- In Situ Hybridization, Fluorescence MeSH
- Real-Time Polymerase Chain Reaction MeSH
- Humans MeSH
- RNA, Messenger genetics MeSH
- Cell Line, Tumor MeSH
- Lung Neoplasms diagnosis genetics MeSH
- Carcinoma, Non-Small-Cell Lung diagnosis genetics MeSH
- Carcinoma, Squamous Cell diagnosis genetics MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- DNA Probes MeSH
- EML4-ALK fusion protein, human MeSH Browser
- Oncogene Proteins, Fusion MeSH
- RNA, Messenger MeSH
OBJECTIVES: Lung cancer with the ALK rearrangement constitutes only a small fraction of patients with non-small cell lung cancer (NSCLC). However, in the era of molecular-targeted therapy, efficient patient selection is crucial for successful treatment. In this context, an effective method for EML4-ALK detection is necessary. We developed a new highly sensitive variant specific TaqMan based real time PCR assay applicable to RNA from formalin-fixed paraffin-embedded tissue (FFPE). MATERIALS AND METHODS: This assay was used to analyze the EML4-ALK gene in 96 non-selected NSCLC specimens and compared with two other methods (end-point PCR and break-apart FISH). RESULTS: EML4-ALK was detected in 33/96 (34%) specimens using variant specific real time PCR, whereas in only 23/96 (24%) using end-point PCR. All real time PCR positive samples were confirmed with direct sequencing. A total of 46 specimens were subsequently analyzed by all three detection methods. Using variant specific real time PCR we identified EML4-ALK transcript in 17/46 (37%) specimens, using end-point PCR in 13/46 (28%) specimens and positive ALK rearrangement by FISH was detected in 8/46 (17.4%) specimens. Moreover, using variant specific real time PCR, 5 specimens showed more than one EML4-ALK variant simultaneously (in 2 cases the variants 1+3a+3b, in 2 specimens the variants 1+3a and in 1 specimen the variant 1+3b). In one case of 96 EML4-ALK fusion gene and EGFR mutation were detected. All simultaneous genetic variants were confirmed using end-point PCR and direct sequencing. CONCLUSION: Our variant specific real time PCR assay is highly sensitive, fast, financially acceptable, applicable to FFPE and seems to be a valuable tool for the rapid prescreening of NSCLC patients in clinical practice, so, that most patients able to benefit from targeted therapy could be identified.
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