Evidence map›Paper›PMID 28122052›Full record

ArticlePloS one2017

A Comparison of RNA-Seq Results from Paired Formalin-Fixed Paraffin-Embedded and Fresh-Frozen Glioblastoma Tissue Samples.

Anna Esteve-Codina, Oriol Arpi, Maria Martinez-García, Estela Pineda, Mar Mallo, Marta Gut, Cristina Carrato, Anna Rovira, Raquel Lopez, Avelina Tortosa and 9 more

Abstract readComparative Study
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 76 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
76citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

76 citing papers in PubMed, 1 synthesis or guideline pooled it.

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  18. ChromogenicNon-coding RNA research · 2024
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16 more citing papers are in PubMed but not listed here.

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

19 authors.

Anna Esteve-CodinaCNAG-CRG,Centre for Genomic Regulation (CRG), Institute of Science and Technology (BIST), Universitat Pompeu Fabra (UPF), Barcelona, Spain.
Oriol ArpiCancer Research Program, Institut Hospital del Mar d'Investigacions Mèdiques (IMIM), Barcelona, Spain.
Maria Martinez-GarcíaMedical Oncology, Hospital del Mar, Barcelona, Spain.
Estela PinedaMedical Oncology, Hospital Clínic, Barcelona, Spain.
Mar MalloInstitut de Recerca Contra la Leucèmia Josep Carreras, Badalona, Barcelona, Spain.
Marta GutSequencing Unit, CNAG-CRG, Centre for Genomic Regulation (CRG), Barcelona Institute of Science and Technology (BIST), Universitat Pompeu Fabra (UPF), Barcelona, Spain.
Cristina CarratoPathology Department, Hospital Universitari Germans Trias i Pujol, Badalona, Barcelona, Spain.
Anna RoviraCancer Research Program, Institut Hospital del Mar d'Investigacions Mèdiques (IMIM), Barcelona, Spain.
Raquel LopezPathology Department, Hospital Josep Trueta, Girona, Spain.
Avelina TortosaLaboratori de quimio-resistència i cáncer, Facultat de Medicina i Ciències de la Salut, Universitat de Barcelona, Departament Infermeria Fonamental, Institut d'Investigacio Biomedica de Bellvitge (IDIBELL), Bellvitge, Barcelona, Spain.
Marc DabadCNAG-CRG,Centre for Genomic Regulation (CRG), Institute of Science and Technology (BIST), Universitat Pompeu Fabra (UPF), Barcelona, Spain.
Sonia Del BarcoMedical Oncology, Institut Català Oncologia (ICO), Hospital Josep Trueta, Girona, Spain.
Simon HeathCNAG-CRG,Centre for Genomic Regulation (CRG), Institute of Science and Technology (BIST), Universitat Pompeu Fabra (UPF), Barcelona, Spain.
Silvia BaguéPathology Department, Hospital de Sant Pau, Barcelona, Spain.
Teresa RibaltaPathology Department (Neuropathology), Hospital Clinic, Barcelona, Spain.
Francesc AlamedaPathology Department, Hospital del Mar, Barcelona, Spain.
Nuria de la IglesiaGlioma and Neural Stem Cell Group, Translational Genomics and Targeted Therapeutics in Solid Tumors Team, August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain.
Carmen BalañaInstitut Català d'Oncologia, Medical Oncology Service, Hospital Germans Trias i Pujol, Badalona, Spain.ORCID http://orcid.org/0000-0003-0771-0390
GLIOCAT Group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The molecular classification of glioblastoma (GBM) based on gene expression might better explain outcome and response to treatment than clinical factors. Whole transcriptome sequencing using next-generation sequencing platforms is rapidly becoming accepted as a tool for measuring gene expression for both research and clinical use. Fresh frozen (FF) tissue specimens of GBM are difficult to obtain since tumor tissue obtained at surgery is often scarce and necrotic and diagnosis is prioritized over freezing. After diagnosis, leftover tissue is usually stored as formalin-fixed paraffin-embedded (FFPE) tissue. However, RNA from FFPE tissues is usually degraded, which could hamper gene expression analysis. We compared RNA-Seq data obtained from matched pairs of FF and FFPE GBM specimens. Only three FFPE out of eleven FFPE-FF matched samples yielded informative results. Several quality-control measurements showed that RNA from FFPE samples was highly degraded but maintained transcriptomic similarities to RNA from FF samples. Certain issues regarding mutation analysis and subtype prediction were detected. Nevertheless, our results suggest that RNA-Seq of FFPE GBM specimens provides reliable gene expression data that can be used in molecular studies of GBM if the RNA is sufficiently preserved.

Indexed as

Gene Expression Regulation, NeoplasticBrain NeoplasmsComputational BiologyGene Expression ProfilingGlioblastomaHigh-Throughput Nucleotide SequencingHumans

Identifiers

PMID28122052
PMCPMC5266269

What OpenQuestion holds

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Registered trials

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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.