Evidence map›Paper›PMID 28287265›Full record

ArticleJournal of proteome research2017

Glycoproteins in Claudin-Low Breast Cancer Cell Lines Have a Unique Expression Profile.

Ten-Yang Yen, Spencer Bowen, Roger Yen, Alexandra Piryatinska, Bruce A Macher, Leslie C Timpe

Open access · greenAbstract read
In one paragraph

Article in Journal of proteome research, 2017. 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
0.5field-weighted citation impact, top 30% 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, 7 citations in OpenAlex.

  1. Dynamic profiling of medulloblastoma surfaceome.Acta neuropathologica communications · 2023
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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

6 authors at 1 institution in 1 country.

Ten-Yang YenDepartment of Chemistry and Biochemistry, ‡Department of Mathematics, §Department of Biology, San Francisco State University , 1600 Holloway Ave., San Francisco, California 94132, United States.
Spencer BowenDepartment of Chemistry and Biochemistry, ‡Department of Mathematics, §Department of Biology, San Francisco State University , 1600 Holloway Ave., San Francisco, California 94132, United States.
Roger YenDepartment of Chemistry and Biochemistry, ‡Department of Mathematics, §Department of Biology, San Francisco State University , 1600 Holloway Ave., San Francisco, California 94132, United States.
Alexandra PiryatinskaDepartment of Chemistry and Biochemistry, ‡Department of Mathematics, §Department of Biology, San Francisco State University , 1600 Holloway Ave., San Francisco, California 94132, United States.
Bruce A MacherDepartment of Chemistry and Biochemistry, ‡Department of Mathematics, §Department of Biology, San Francisco State University , 1600 Holloway Ave., San Francisco, California 94132, United States.
Leslie C TimpeDepartment of Chemistry and Biochemistry, ‡Department of Mathematics, §Department of Biology, San Francisco State University , 1600 Holloway Ave., San Francisco, California 94132, United States.ORCID 0000-0002-2398-4765
San Francisco State University · US

Funding

Student EnrichmentP20MD000544 · NIMHD · SAN FRANCISCO STATE UNIVERSITY · PI BAIRD, TEASTER T · 2003 to 2012
$9.4M
Glycoprotein Signatures as Biomarkers for Breast CancerR15CA164929 · NCI · SAN FRANCISCO STATE UNIVERSITY · PI MACHER, BRUCE A., TIMPE, LESLIE CHARLES · 2012 to 2012
$462k
NCI NIH HHS R15 CA164929NIMHD NIH HHS P20 MD000544
6 · The paper itself

Abstract

Claudin proteins are components of epithelial tight junctions; a subtype of breast cancer has been defined by the reduced expression of mRNA for claudins and other genes. Here, we characterize the expression of glycoproteins in breast cell lines for the claudin-low subtype using liquid chromatography/tandem mass spectrometry. Unsupervised clustering techniques reveal a group of claudin-low cell lines that is distinct from nonmalignant, basal, and luminal lines. The claudin-low cell lines express F11R, EPCAM, and other proteins at very low levels, whereas CD44 is expressed at a high level. Comparison of mRNA expression to glycoprotein expression shows modest correlation; the best agreement occurs when the mRNA expression level is lowest and little or no protein is detected. These findings from cell lines are compared to those for tumor samples by the Clinical Proteomic Tumor Analysis Consortium (CPTAC). The CPTAC samples contain a group low in CLDN3. The samples low in CLDN3 proteins share many differentially expressed glycoproteins with the claudin-low cell lines. In contrast to the situation for cell lines or patient samples classified as claudin-low by RNA expression, however, most of the tumor samples low in CLDN3 protein express the estrogen receptor or HER2. These tumor samples express CD44 protein at low rather than high levels. There is no correlation between CLDN3 gene expression and protein expression in these CPTAC samples; hence, the claudin-low subtype defined by gene expression is not the same group of tumors as that defined by low expression of CLDN3 protein.

Indexed as

Biomarkers, TumorBreast NeoplasmsCell Line, TumorClaudin-3Erb-b2 Receptor Tyrosine KinasesFemaleGene Expression Regulation, NeoplasticGlycoproteinsHumansHyaluronan ReceptorsMass SpectrometryPrognosisProteomicsBiomarkers, TumorCD44 protein, humanClaudin-3CLDN3 protein, humanERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesGlycoproteinsHyaluronan Receptorsbreast cancercell linesclaudinglycoproteinmass spectrometrysupervised classification

Identifiers

PMID28287265
PMCPMC5557415
OpenAlexW2596851559

What OpenQuestion holds

Textmetadata
LicenceTDM
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.