Evidence map›Paper›PMID 34209696›Full record

ArticleInternational journal of molecular sciences2021

CD74 and CD44 Expression on CTCs in Cancer Patients with Brain Metastasis.

Desiree Loreth, Moritz Schuette, Jenny Zinke, Malte Mohme, Andras Piffko, Svenja Schneegans, Julia Stadler, Melanie Janning, Sonja Loges, Simon A Joosse and 14 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
6.8field-weighted citation impact, top 2% 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

36 citing papers in PubMed, 51 citations in OpenAlex.

  1. Article
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  4. Protein Marker-Dependent Drug Discovery Targeting Breast Cancer Stem Cells.International journal of molecular sciences · 2025
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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

24 authors at 4 institutions in 1 country.

Desiree LorethDepartment of Tumor Biology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.ORCID 0000-0003-0827-149X
Moritz SchuetteAlacris Theranostics GmbH, Max-Planck-Straße 3, 12489 Berlin, Germany.
Jenny ZinkeInstitute of Neurology (Edinger Institute), Goethe University, 60528 Frankfurt am Main, Germany.
Malte MohmeDepartment of Neurosurgery, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
Andras PiffkoDepartment of Neurosurgery, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.ORCID 0000-0001-5300-6594
Svenja SchneegansDepartment of Tumor Biology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.ORCID 0000-0002-2684-790X
Julia StadlerDepartment of Dermatology and Venerology, University Hospital Hamburg-Eppendorf, 20246 Hamburg, Germany.ORCID 0000-0001-5653-8414
Melanie JanningDivision of Personalized Medical Oncology (A420), German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany.
Sonja LogesDivision of Personalized Medical Oncology (A420), German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany.
Simon A JoosseDepartment of Tumor Biology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.ORCID 0000-0002-4296-5615
Katrin LamszusDepartment of Neurosurgery, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
Manfred WestphalDepartment of Neurosurgery, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
Volkmar MüllerDepartment of Gynecology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.ORCID 0000-0003-4231-7906
Markus GlatzelDepartment of Neuropathology, University Medical Centre Hamburg-Eppendorf, 20246 Hamburg, Germany.ORCID 0000-0002-7720-8817
Jakob MatschkeDepartment of Neuropathology, University Medical Centre Hamburg-Eppendorf, 20246 Hamburg, Germany.
Christoffer GebhardtDepartment of Dermatology and Venerology, University Hospital Hamburg-Eppendorf, 20246 Hamburg, Germany.ORCID 0000-0001-7090-9584
Stefan W SchneiderDepartment of Dermatology and Venerology, University Hospital Hamburg-Eppendorf, 20246 Hamburg, Germany.
Iwona BelczackaOtto Warburg Laboratory Gene Regulation and Systems Biology of Cancer, Max Planck Institute for Molecular Genetics, 14195 Berlin, Germany.
Beate VolkmerAssociation of Dermatological Prevention, Germany & Centre of Dermatology, Elbe Clinics, 21614 Buxtehude, Germany.ORCID 0000-0001-9218-8650
Rüdiger GreinertAssociation of Dermatological Prevention, Germany & Centre of Dermatology, Elbe Clinics, 21614 Buxtehude, Germany.
Marie-Laure YaspoOtto Warburg Laboratory Gene Regulation and Systems Biology of Cancer, Max Planck Institute for Molecular Genetics, 14195 Berlin, Germany.
Patrick N HarterInstitute of Neurology (Edinger Institute), Goethe University, 60528 Frankfurt am Main, Germany.
Klaus PantelDepartment of Tumor Biology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.ORCID 0000-0001-5736-2772
Harriet WikmanDepartment of Tumor Biology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.ORCID 0000-0001-6862-0888
Universität Hamburg · DEGoethe University Frankfurt · DEMax Planck Institute for Molecular Genetics · DEAlacris (Germany) · DE

Funding

Deutsche Krebshilfe 70112507Wilhelm-Sander Stiftung 2017.142.1
6 · The paper itself

Abstract

Up to 40% of advance lung, melanoma and breast cancer patients suffer from brain metastases (BM) with increasing incidence. Here, we assessed whether circulating tumor cells (CTCs) in peripheral blood can serve as a disease surrogate, focusing on CD44 and CD74 expression as prognostic markers for BM. We show that a size-based microfluidic approach in combination with a semi-automated cell recognition system are well suited for CTC detection in BM patients and allow further characterization of tumor cells potentially derived from BM. CTCs were found in 50% (7/14) of breast cancer, 50% (9/18) of non-small cell lung cancer (NSCLC) and 36% (4/11) of melanoma patients. The next-generation sequencing (NGS) analysis of nine single CTCs from one breast cancer patient revealed three different CNV profile groups as well as a resistance causing ERS1 mutation. CD44 and CD74 were expressed on most CTCs and their expression was strongly correlated, whereas matched breast cancer BM tissues were much less frequently expressing CD44 and CD74 (negative in 46% and 54%, respectively). Thus, plasticity of CD44 and CD74 expression during trafficking of CTCs in the circulation might be the result of adaptation strategies.

Indexed as

Antigens, Differentiation, B-LymphocyteBiomarkers, TumorBrain NeoplasmsBreast NeoplasmsCarcinoma, Non-Small-Cell LungCell Line, TumorFemaleHistocompatibility Antigens Class IIHumansHyaluronan ReceptorsImmunohistochemistryMaleMutationNeoplastic Cells, CirculatingWhole Genome SequencingAntigens, Differentiation, B-LymphocyteBiomarkers, TumorCD44 protein, humanHistocompatibility Antigens Class IIHyaluronan Receptorsinvariant chainbrain metastasisbreast cancercirculating tumor cellsmelanomaNSCLC

Identifiers

PMID34209696
PMCPMC8268634
OpenAlexW3176889573

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.