Evidence map›Paper›PMID 28436954›Full record

ArticleLaboratory investigation; a journal of technical methods and pathology2017

Optimized expression-based microdissection of formalin-fixed lung cancer tissue.

Markus Grafen, Thurid R Hofmann, Andreas H Scheel, Julia Beck, Alexander Emmert, Stefan Küffer, Bernhard C Danner, Ekkehard Schütz, Reinhardt Büttner, Andreas Ostendorf and 2 more

Open access · hybridAbstract read
PubMed Publisher
In one paragraph

Article in Laboratory investigation; a journal of technical methods and pathology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 50% 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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. The somatic molecular evolution of cancer: Mutation, selection, and epistasis.Progress in biophysics and molecular biology · 2021
    Article
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

12 authors at 3 institutions in 1 country.

Markus GrafenApplied Laser Technologies, Faculty of Mechanical Engineering, Ruhr-University Bochum, Bochum, Germany.
Thurid R HofmannInstitute of Pathology, University Medical Center, Georg-August-University Göttingen, Göttingen, Germany.
Andreas H ScheelInstitute of Pathology, University Hospital Cologne, University of Cologne, Köln, Germany.
Julia BeckChronix Biomedical, Goetheallee 8, Göttingen, Germany.
Alexander EmmertDepartment of Thoracic and Cardiovascular Surgery, University Medical Center, Georg-August-University Göttingen, Göttingen, Germany.
Stefan KüfferInstitute of Pathology, University Medical Center, Georg-August-University Göttingen, Göttingen, Germany.
Bernhard C DannerDepartment of Thoracic and Cardiovascular Surgery, University Medical Center, Georg-August-University Göttingen, Göttingen, Germany.
Ekkehard SchützChronix Biomedical, Goetheallee 8, Göttingen, Germany.
Reinhardt BüttnerInstitute of Pathology, University Hospital Cologne, University of Cologne, Köln, Germany.
Andreas OstendorfApplied Laser Technologies, Faculty of Mechanical Engineering, Ruhr-University Bochum, Bochum, Germany.
Philipp StröbelInstitute of Pathology, University Medical Center, Georg-August-University Göttingen, Göttingen, Germany.
Hanibal BohnenbergerInstitute of Pathology, University Medical Center, Georg-August-University Göttingen, Göttingen, Germany.
University of Göttingen · DERuhr University Bochum · DEUniversity of Cologne · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Analysis of specific DNA alterations in precision medicine of tumors is crucially important for molecular targeted treatments. Lung cancer is a prototypic example and one of the leading causes of cancer-related deaths worldwide. One major technical problem of detecting DNA alterations in tissue samples is cellular heterogeneity, that is, mixture of tumor and normal cells. Microdissection is an important tool to enrich tumor cells from heterogeneous tissue samples. However, conventional laser capture microdissection has several disadvantages like user-dependent selection of regions of interest (ROI), high costs for dissection systems and long processing times. ROI selection in expression-based microdissection (xMD) directly relies on cancer cell-specific immunostaining. Whole-slide irradiation leads to localized energy absorption at the sites of most intensive staining and melting of a membrane covering the slide, so that tumor cells can be isolated by removing the complete membrane. In this study, we optimized xMD of lung cancer tissue by enhancing staining intensity of tumor cell-specific immunostaining and processing of the stained samples. This optimized procedure did not alter DNA quality and resulted in enrichment of mutated EGFR DNA from lung adenocarcinoma specimens after xMD. We here also introduce a quality control protocol based on digital whole-slide scanning and image analysis before and after xMD to quantify selectivity and efficiency of the procedure. In summary, this study provides a workflow for xMD, adapted and tested for lung cancer tissue that can be used for lung tumor cell dissection before diagnostic or investigatory analyses.

Indexed as

AdenocarcinomaAdenocarcinoma of LungDNAFormaldehydeHumansImmunohistochemistryLungLung NeoplasmsMicrodissectionMolecular Diagnostic TechniquesMutationStaining and LabelingTissue FixationDNAFormaldehyde

Identifiers

PMID28436954
OpenAlexW2608979646

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.