Evidence map›Paper›PMID 41915220›Full record

ReviewPathologie (Heidelberg, Germany)2026

[Proteomics and glycomics in pathology : Potential of autopsy and FFPE tissue for diagnostics and research].

Falk Buettner, Rainer Claus

Abstract readEnglish AbstractReview
PubMed Publisher
In one paragraph

Review in Pathologie (Heidelberg, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

Falk BuettnerProteinanalytik, Universität Augsburg, Universitätsstraße 2, 86159, Augsburg, Deutschland. falk.buettner@med.uni-augsburg.de.ORCID http://orcid.org/0000-0002-8468-1223
Rainer ClausInstitut für Pathologie und Molekulare Diagnostik, Comprehensive Cancer Center Augsburg (CCCA), Universitätsklinikum Augsburg, Stenglinstr. 2, 86156, Augsburg, Deutschland. rainer.claus@uk-augsburg.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The repertoire of disease-associated, formalin-fixed, paraffin-embedded (FFPE) samples collected and archived over decades is vast. When combined with frequently available and detailed clinical information on patients, disease progression, and outcomes, these samples represent a unique resource for investigating disease mechanisms at the molecular level. However, due to the specific sample preparation process, which involves chemical modifications of the tissue, the direct use of FFPE material in many analytical procedures has been limited.This review article reports on advances in analytical methods from the fields of proteomics and glycomics for the use of FFPE samples. A particular focus is placed on the analytical approach we developed for glycan headgroups of glycosphingolipids. Glycosphingolipids are components of the outer plasma membrane whose sugar chains extend into the extracellular space and are highly diverse and complexly regulated. Their glycosylation reflects the cellular state and mirrors pathological changes.The analytical characterization of glycosphingolipid glycans is challenging and has not yet been part of routine diagnostics. In this article, we describe a sample preparation strategy for FFPE tissue that preserves the characteristic glycosphingolipid repertoire and enables analysis by capillary gel electrophoresis coupled to laser-induced fluorescence detection (CGE-LIF). Using this approach, we identified a novel glycosphingolipid-based biomarker for bladder cancer in patient urine, which is also enriched in corresponding tumor FFPE samples.The goal of this article is to demonstrate the potential of FFPE and autopsy samples for systematic molecular analyses. This methodological combination opens access to extensive FFPE archives and enables the study of glycosphingolipid glycosylation in various tissues and diseases, facilitating the identification of new biomarkers and providing deeper insights into disease mechanisms.

Indexed as

GlycomicsParaffin EmbeddingProteomicsTissue FixationAutopsyFormaldehydeGlycosphingolipidsHumansFormaldehydeGlycosphingolipidsBiomarkersCGE-LIFFFPEGlycosphingolipidsMass spectrometry

Identifiers

PMID41915220

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.