Evidence map›Paper›PMID 27399691›Full record

ArticleInternational journal of molecular sciences2016

MALDI Mass Spectrometry Imaging Reveals Decreased CK5 Levels in Vulvar Squamous Cell Carcinomas Compared to the Precursor Lesion Differentiated Vulvar Intraepithelial Neoplasia.

Chao Zhang, Georgia Arentz, Lyron Winderbaum, Noor A Lokman, Manuela Klingler-Hoffmann, Parul Mittal, Christopher Carter, Martin K Oehler, Peter Hoffmann

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

8 citing papers in PubMed, 13 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 3 institutions in 1 country.

Chao ZhangAdelaide Proteomics Centre, School of Biological Sciences, The University of Adelaide, Adelaide 5005, Australia. chao.zhang01@student.adelaide.edu.au.
Georgia ArentzAdelaide Proteomics Centre, School of Biological Sciences, The University of Adelaide, Adelaide 5005, Australia. georgia.arentz@adelaide.edu.au.
Lyron WinderbaumAdelaide Proteomics Centre, School of Biological Sciences, The University of Adelaide, Adelaide 5005, Australia. lyron.winderbaum@student.adelaide.edu.au.
Noor A LokmanAdelaide Proteomics Centre, School of Biological Sciences, The University of Adelaide, Adelaide 5005, Australia. noor.lokman@adelaide.edu.au.
Manuela Klingler-HoffmannAdelaide Proteomics Centre, School of Biological Sciences, The University of Adelaide, Adelaide 5005, Australia. manuela.klinglerhoffmann@adelaide.edu.au.
Parul MittalAdelaide Proteomics Centre, School of Biological Sciences, The University of Adelaide, Adelaide 5005, Australia. parul.mittal@adelaide.edu.au.
Christopher CarterDepartment of Cytopathology, SA Pathology, Adelaide 5005, Australia. Christopher.Carter@sa.gov.au.
Martin K OehlerDiscipline of Obstetrics and Gynaecology, School of Medicine, Research Centre for Reproductive Health, Robinson Institute, Adelaide 5005, Australia. martin.oehler@adelaide.edu.au.
Peter HoffmannAdelaide Proteomics Centre, School of Biological Sciences, The University of Adelaide, Adelaide 5005, Australia. Peter.hoffmann@adelaide.edu.au.
The University of Adelaide · AURoyal Adelaide Hospital · AUSouth Australia Pathology · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Vulvar cancer is the fourth most common gynecological cancer worldwide. However, limited studies have been completed on the molecular characterization of vulvar squamous cell carcinoma resulting in a poor understanding of the disease initiation and progression. Analysis and early detection of the precursor lesion of HPV-independent vulvar squamous cell carcinoma (VSCC), differentiated vulvar intraepithelial neoplasia (dVIN), is of great importance given dVIN lesions have a high level of malignant potential. Here we present an examination of adjacent normal vulvar epithelium, dVIN, and VSCC from six patients by peptide Matrix-assisted laser desorption/ionization Mass Spectrometry Imaging (MALDI-MSI). The results reveal the differential expression of multiple peptides from the protein cytokeratin 5 (CK5) across the three vulvar tissue types. The difference observed in the relative abundance of CK5 by MALDI-MSI between the healthy epithelium, dVIN, and VSCC was further analyzed by immunohistochemistry (IHC) in tissue from eight VSCC patients. A decrease in CK5 immunostaining was observed in the VSCC compared to the healthy epithelium and dVIN. These results provide an insight into the molecular fingerprint of the vulvar intraepithelial neoplasia that appears to be more closely related to the healthy epithelium than the VSCC.

Indexed as

Spectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationAdultAgedAged, 80 and overCarcinoma, Squamous CellChromatography, High Pressure LiquidEpitheliumFemaleHumansImmunohistochemistryKeratin-5Middle AgedNeoplasm StagingPeptidesVulvar NeoplasmsKeratin-5PeptidesCytokeratin 5 (CK5)differentiated vulvar intraepithelial neoplasia (dVIN)imaging mass spectrometry (MSI)Matrix-assisted laser desorption/ionization (MALDI)vulva squamous cell carcinomas (VSCC)

Identifiers

PMID27399691
PMCPMC4964464
OpenAlexW2469861206

What OpenQuestion holds

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LicenceCC BY
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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.