Evidence map›Paper›PMID 29706640›Full record

ArticleEuropean journal of human genetics : EJHG2018

RNA analysis of cancer predisposing genes in formalin-fixed paraffin-embedded tissue determines aberrant splicing.

Anne Ml Jansen, Heleen M van der Klift, Marieke Ae Roos, Jaap Dh van Eendenburg, Carli Mj Tops, Juul T Wijnen, Frederik J Hes, Hans Morreau, Tom van Wezel

Open access · bronzeAbstract read
In one paragraph

Article in European journal of human genetics : EJHG, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.8field-weighted citation impact, top 28% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 5 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 1 institution in 1 country.

Anne Ml JansenDepartment of Pathology, Leiden University Medical Center, Leiden, The Netherlands.ORCID http://orcid.org/0000-0002-8793-0563
Heleen M van der KliftDepartment of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.
Marieke Ae RoosDepartment of Pathology, Leiden University Medical Center, Leiden, The Netherlands.
Jaap Dh van EendenburgDepartment of Pathology, Leiden University Medical Center, Leiden, The Netherlands.
Carli Mj TopsDepartment of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.
Juul T WijnenDepartment of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.
Frederik J HesDepartment of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.ORCID http://orcid.org/0000-0002-3025-0882
Hans MorreauDepartment of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands.
Tom van WezelDepartment of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands. t.van_wezel@lumc.nl.ORCID http://orcid.org/0000-0001-5773-7730
Leiden University Medical Center · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

High-throughput sequencing efforts in molecular tumour diagnostics detect increasing numbers of novel variants, including variants predicted to affect splicing. In silico prediction tools can reliably predict the effect of variant disrupting canonical splice sites; however, experimental validation is required to confirm aberrant splicing. Here, we present RNA analysis performed for 13 canonical splice site variants predicted or known to result in splicing in the cancer predisposition genes MLH1, MSH2, MSH6, APC and BRCA1. Total nucleic acid was successfully isolated for 10 variants from eight formalin-fixed paraffin-embedded (FFPE) tumour tissues and two B-cell lines. Aberrant splicing was confirmed in all six variants known to result in splicing. Of one known variant in the B-cell line, aberrant splicing could only be detected after formalin fixation, which indicated that formalin fixation could possibly inhibit RNA degradation. Aberrant splicing was concluded in three of four predicted splice variants of uncertain significance, supporting their pathogenic effect. With this assay, somatic splice variants can be easily and rapidly analysed, enabling retrospective analysis to support the pathogenicity of variants predicted to result in splicing when only FFPE material is available.

Indexed as

MutationRNA SplicingAdenomatous Polyposis Coli ProteinBRCA1 ProteinBreast NeoplasmsDNA-Binding ProteinsFemaleGenetic TestingHumansMutL Protein Homolog 1MutS Homolog 2 ProteinSequence Analysis, RNATissue EmbeddingTissue FixationAdenomatous Polyposis Coli ProteinAPC protein, humanBRCA1 ProteinBRCA1 protein, humanDNA-Binding ProteinsG-T mismatch-binding proteinMLH1 protein, humanMSH2 protein, humanMutL Protein Homolog 1MutS Homolog 2 Protein

Identifiers

PMID29706640
PMCPMC6057924
OpenAlexW2801935789

What OpenQuestion holds

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Registered trials

None linked

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.