Evidence map›Paper›PMID 32426042›Full record

ArticleTherapeutic advances in medical oncology2020

CXCR4 and JUNB double-positive disseminated tumor cells are detected frequently in breast cancer patients at primary diagnosis.

Galatea Kallergi, Oliver Hoffmann, Ann-Kathrin Bittner, Lina Papadimitriou, Spyridoula D Katsarou, Nefeli Zacharopoulou, Michalis Zervakis, Stelios Sfakianakis, Christos Stournaras, Vassilis Georgoulias and 2 more

Open access · goldAbstract read
In one paragraph

Article in Therapeutic advances in medical oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.8field-weighted citation impact, top 25% 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

10 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Observational
  10. Systematic Evaluation ofFrontiers in immunology · 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 5 institutions in 2 countries.

Galatea KallergiDepartment of Biology,University of Patras, 26504, Greece.
Oliver HoffmannDepartment of Gynecology and Obstetrics, University Hospital Essen, Essen, Germany.
Ann-Kathrin BittnerDepartment of Gynecology and Obstetrics, University Hospital Essen, Essen, Germany.
Lina PapadimitriouInstitute of Electronic Structure and Laser, Foundation for Research and Technology-Hellas, (IESL-FORTH), Heraklion, Greece.
Spyridoula D KatsarouDepartment of Biochemistry, Medical School, University of Crete, Heraklion, Greece.
Nefeli ZacharopoulouDepartment of Biochemistry, Medical School, University of Crete, Heraklion, Greece.
Michalis ZervakisDigital Image and Signal Processing Laboratory, School of Electrical and Computer Engineering, Technical University of Crete, Chania, Greece.
Stelios SfakianakisInstitute of Computer Science, Foundation for Research and Technology-Hellas, (IESL-FORTH), Heraklion, Greece.
Christos StournarasDepartment of Biochemistry, Medical School, University of Crete, Heraklion, Greece.
Vassilis GeorgouliasHellenic Oncology Research Group (HORG), Athens, Greece.
Rainer KimmigDepartment of Gynecology and Obstetrics, University Hospital Essen, Essen, Germany.
Sabine Kasimir-BauerDepartment of Gynecology and Obstetrics, University Hospital Essen, Essen, Germany.
Essen University Hospital · DEUniversity of Crete · GRFoundation for Research and Technology Hellas · GRHellenic Oncology Research Group · GRTechnical University of Crete · GR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe chemokine receptor CXCR4 and the transcription factor JUNB, expressed on a variety of tumor cells, seem to play an important role in the metastatic process. Since disseminated tumor cells (DTCs) in the bone marrow (BM) have been associated with worse outcomes, we evaluated the expression of CXCR4 and JUNB in DTCs of primary, nonmetastatic breast cancer (BC) patients before the onset of any systemic treatment.

methodsBilateral BM (10 ml) aspirations of 39 hormone receptor (HR)-positive, HER2-negative BC patients were assessed for the presence of DTCs using the following combination of antibodies: pan-cytokeratin (A45-B/B3)/CXCR4/JUNB. An expression pattern of the examined proteins was created using confocal laser scanning microscopy, Image J software and BC cell lines.

resultsCXCR4 was overexpressed in cancer cells and DTCs, with the following hierarchy of expression: SKBR3 > MCF7 > DTCs > MDA-MB231. Accordingly, the expression pattern of JUNB was: DTCs > MDA-MB231 > SKBR3 > MCF7. The mean intensity of CXCR4 (6411 ± 334) and JUNB (27725.64 ± 470) in DTCs was statistically higher compared with BM hematopoietic cells (2009 ± 456,

conclusions(CXCR4+JUNB+CK+)-expressing DTCs, detected frequently in the BM of BC patients, seem to identify a subgroup of patients at higher risk for relapse that may be considered for close follow up.

Indexed as

CXCR4disseminated tumor cellsdormancyJUNBprimary breast cancer

Identifiers

PMID32426042
PMCPMC7222234
OpenAlexW3021730173

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.