Evidence map›Paper›PMID 39537990›Full record

ArticleVirchows Archiv : an international journal of pathology2025

Sensitive and reliable detection of KIT p.D816V mutation in decalcified archival bone marrow trephines.

Miriam Odensass, Stephan Bartels, Jerome Schlue, Guntram Büsche, Hans H Kreipe, Ulrich Lehmann

Abstract read
In one paragraph

Article in Virchows Archiv : an international journal of pathology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Miriam OdensassInstitute of Pathology, Hannover Medical School, Carl-Neuberg-Str. 1, 30625, Hannover, Germany.
Stephan BartelsInstitute of Pathology, Hannover Medical School, Carl-Neuberg-Str. 1, 30625, Hannover, Germany.
Jerome SchlueInstitute of Pathology, Hannover Medical School, Carl-Neuberg-Str. 1, 30625, Hannover, Germany.
Guntram BüscheInstitute of Pathology, Hannover Medical School, Carl-Neuberg-Str. 1, 30625, Hannover, Germany.
Hans H KreipeInstitute of Pathology, Hannover Medical School, Carl-Neuberg-Str. 1, 30625, Hannover, Germany.
Ulrich LehmannInstitute of Pathology, Hannover Medical School, Carl-Neuberg-Str. 1, 30625, Hannover, Germany. Lehmann.Ulrich@MH-Hannover.de.ORCID http://orcid.org/0000-0003-2350-6584

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The majority of mastocytosis cases are characterized by an activating mutation in the KIT gene in codon 816. The detection of this alteration is of importance for proper diagnostic workup. Therefore, reliable and sensitive methods for the detection of KIT Codon 816 hotspot mutations in various types of patient samples are required. Since mutated cancer genes are often overexpressed, we evaluated the feasibility and sensitivity of KIT p.D816V detection by analysing mRNA/cDNA instead of genomic DNA. From 80 bone marrow trephines harboring a KIT p.D816 mutation, seven were only mutated by mRNA/cDNA pyrosequencing and 11 only by digital PCR analysis of genomic DNA. These results clearly demonstrate that detection of clinically relevant mutations in mRNA extracted from routinely processed decalcified archival bone marrow trephines is not only possible in a reliable fashion but under many circumstances advantageous. This enables the direct correlation of genomic data with high-quality morphological evaluation.

Indexed as

Bone MarrowMastocytosis, SystemicMutationProto-Oncogene Proteins c-kitAdultAgedDNA Mutational AnalysisFemaleHumansMaleMiddle AgedKIT protein, humanProto-Oncogene Proteins c-kitBone marrow trephinesKIT p.D816VMRNASystemic mastocytosis

Identifiers

PMID39537990
PMCPMC12213911

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.