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dc.contributor.authorKriegsmann, Mark
dc.contributor.authorArens, Norbert
dc.contributor.authorEndris, Volker
dc.contributor.authorWeichert, Wilko
dc.contributor.authorKriegsmann, Jörg
dc.date.accessioned2015-09-01T17:02:18Z
dc.date.available2015-09-01T17:02:18Z
dc.date.issued2015-07-30
dc.identifier.citationDiagnostic Pathology. 2015 Jul 30;10(1):132
dc.identifier.urihttp://dx.doi.org/10.1186/s13000-015-0364-3
dc.identifier.urihttp://hdl.handle.net/10724/31711
dc.description.abstractAbstract Background According to current clinical guidelines mutational analysis for KRAS and NRAS is recommended prior to EGFR-directed therapy of colorectal cancer (CRC) in the metastatic setting. Therefore, reliable, fast, sensitive and cost-effective methods for routine tissue based molecular diagnostics are required that allow the assessment of the CRC mutational status in a high throughput fashion. Methods We have developed a custom designed assay for routine mass-spectrometric (MS) (MassARRAY®, Agena Bioscience) analysis to test the presence/absence of 18 KRAS, 14 NRAS and 4 BRAF mutations. We have applied this assay to 93 samples from patients with CRC and have compared the results with Sanger sequencing and a chip hybridization assay (KRAS LCD-array Kit, Chipron). In cases with discordant results, next-generation sequencing (NGS) was performed. Results MS detected a KRAS mutation in 46/93 (49 %), a NRAS mutation in 2/93 (2 %) and a BRAF mutation in 1/93 (1 %) of the cases. MS results were in agreement with results obtained by combination of the two other methods in 92 (99 %) of 93 cases. In 1/93 (1 %) of the cases a G12V mutation has been detected by Sanger sequencing and MS, but not by the chip assay. In this case, NGS has confirmed the G12V mutation in KRAS. Conclusions Mutational analysis by MS is a reliable method for routine diagnostic use, which can be easily extended for testing of additional mutations.
dc.titleDetection of KRAS, NRAS and BRAF by mass spectrometry - a sensitive, reliable, fast and cost-effective technique
dc.typeJournal Article
dc.date.updated2015-07-29T18:18:12Z
dc.language.rfc3066en
dc.rights.holderKriegsmann et al.


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