Evidence map›Paper›PMID 27141386›Full record

ArticleOncoimmunology2016

Gene expression profiling of circulating tumor cells and peripheral blood mononuclear cells from breast cancer patients.

Michal Hensler, Irena Vančurová, Etienne Becht, Ondřej Palata, Pavel Strnad, Petra Tesařová, Michaela Čabiňaková, David Švec, Mikael Kubista, Jiřina Bartůňková and 2 more

Open access · goldAbstract read
In one paragraph

Article in Oncoimmunology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.0field-weighted citation impact, top 11% 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

24 citing papers in PubMed, 37 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

12 authors at 6 institutions in 3 countries.

Michal HenslerSotio, a.s. , Prague, Czech Republic.
Irena VančurováSotio, a.s., Prague, Czech Republic; Department of Immunology, Charles University, Second Faculty of Medicine and University Hospital Motol, Prague, Czech Republic.
Etienne BechtLaboratory of Cancer, Immune Control and Escape, UMRS 1138 INSERM, Cordeliers Research Center , Paris, France.
Ondřej PalataSotio, a.s. , Prague, Czech Republic.
Pavel StrnadDepartment of Gynecology and Obstetrics, Second Faculty of Medicine, Charles University and University Hospital Motol , Prague, Czech Republic.
Petra TesařováOncology Clinic, First Faculty of Medicine, Charles University , Prague, Czech Republic.
Michaela ČabiňakováOncology Clinic, First Faculty of Medicine, Charles University , Prague, Czech Republic.
David ŠvecTATAA Biocenter, Göteborg, Sweden; Laboratory of Gene Expression, Institute of Biotechnology, Academy of Sciences of the Czech Republic, v.v.i., Prague, Czech Republic.
Mikael KubistaTATAA Biocenter, Göteborg, Sweden; Laboratory of Gene Expression, Institute of Biotechnology, Academy of Sciences of the Czech Republic, v.v.i., Prague, Czech Republic.
Jiřina BartůňkováSotio, a.s., Prague, Czech Republic; Department of Immunology, Charles University, Second Faculty of Medicine and University Hospital Motol, Prague, Czech Republic.
Radek ŠpíšekSotio, a.s., Prague, Czech Republic; Department of Immunology, Charles University, Second Faculty of Medicine and University Hospital Motol, Prague, Czech Republic.
Luděk SojkaSotio, a.s., Prague, Czech Republic; Department of Immunology, Charles University, Second Faculty of Medicine and University Hospital Motol, Prague, Czech Republic.
Charles University · CZSotio (Czechia) · CZUniversity Hospital in Motol · CZCzech Academy of Sciences · CZInserm · FRTataa Biocenter (Sweden) · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Circulating tumor cells (CTCs) are cancer cells that are released from a tumor into the bloodstream. The presence of CTCs in peripheral blood has been associated with metastasis formation in patients with breast cancer. Therefore, the molecular characterization of CTCs may improve diagnostics and support treatment decisions. We performed gene expression profiling to evaluate the enriched CTCs and peripheral blood mononuclear cells (PBMCs) of breast cancer patients using an expression panel of 55 breast cancer-associated genes. The study revealed several significantly differentially expressed genes in the CTC-positive samples, including a few that were exclusively expressed in these cells. However, the expression of these genes was barely detectable in the PBMC samples. Some genes were differentially expressed in PBMCs, and the expression of these genes was correlated with tumor grade and the formation of metastasis. In this study, we have shown that the enriched CTCs of breast cancer patients overexpress genes involved in proteolytic degradation of the extracellular matrix (ECM) as well as genes that play important roles in the epithelial-mesenchymal transition (EMT) process that may occur in these cells.

Indexed as

Breast cancer, circulating tumor cellsgene expression profilingperipheral blood mononuclear cellsprognostic

Identifiers

PMID27141386
PMCPMC4839342
OpenAlexW2252648034

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.