Evidence map›Paper›PMID 36012587›Full record

ArticleInternational journal of molecular sciences2022

Red Blood Cell-Derived Microparticles Exert No Cancer Promoting Effects on Colorectal Cancer Cells In Vitro.

Dania Fischer, Fabian Thies, Omar Awad, Camilla Brat, Patrick Meybohm, Patrick C Baer, Markus M Müller, Anja Urbschat, Thorsten J Maier, Kai Zacharowski and 1 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.1field-weighted citation impact, top 57% 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

2 citing papers in PubMed, 1 citations in OpenAlex.

  1. Article
  2. Review
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

11 authors at 3 institutions in 1 country.

Dania FischerDepartment of Anesthesiology, Intensive Care Medicine and Pain Therapy, University Hospital Frankfurt, Goethe University, 60590 Frankfurt am Main, Germany.
Fabian ThiesDepartment of Anesthesiology, Intensive Care Medicine and Pain Therapy, University Hospital Frankfurt, Goethe University, 60590 Frankfurt am Main, Germany.
Omar AwadDepartment of Safety of Medicinal Products and Medical Devices, Paul-Ehrlich-Institute (Federal Institute for Vaccines and Biomedicines), 63225 Langen, Germany.
Camilla BratDepartment of Anesthesiology, Intensive Care Medicine and Pain Therapy, University Hospital Frankfurt, Goethe University, 60590 Frankfurt am Main, Germany.
Patrick MeybohmDepartment of Anesthesiology, Intensive Care Medicine and Pain Therapy, University Hospital Frankfurt, Goethe University, 60590 Frankfurt am Main, Germany.ORCID 0000-0002-2666-8696
Patrick C BaerClinic of Internal Medicine III, Division of Nephrology, University Hospital Frankfurt, 60590 Frankfurt am Main, Germany.ORCID 0000-0001-8113-3312
Markus M MüllerGerman Red Cross Blood Transfusion Service and Goethe University Clinics, 60590 Frankfurt am Main, Germany.
Anja UrbschatClinic of Urology and Pediatric Urology, Philipps University of Marburg, 35043 Marburg, Germany.
Thorsten J MaierDepartment of Safety of Medicinal Products and Medical Devices, Paul-Ehrlich-Institute (Federal Institute for Vaccines and Biomedicines), 63225 Langen, Germany.
Kai ZacharowskiDepartment of Anesthesiology, Intensive Care Medicine and Pain Therapy, University Hospital Frankfurt, Goethe University, 60590 Frankfurt am Main, Germany.ORCID 0000-0002-0212-9110
Jessica RoosDepartment of Anesthesiology, Intensive Care Medicine and Pain Therapy, University Hospital Frankfurt, Goethe University, 60590 Frankfurt am Main, Germany.
Goethe University Frankfurt · DEPaul Ehrlich Institut · DEPhilipps University of Marburg · DE

Funding

Faculty of Medicine, Goethe University, Frankfurt am Main, Germany Young Investigator Grant
6 · The paper itself

Abstract

The biomedical consequences of allogeneic blood transfusions and the possible pathomechanisms of transfusion-related morbidity and mortality are still not entirely understood. In retrospective studies, allogeneic transfusion was associated with increased rates of cancer recurrence, metastasis and death in patients with colorectal cancer. However, correlation does not imply causation. The purpose of this study was to elucidate this empirical observation further in order to address insecurity among patients and clinicians. We focused on the in vitro effect of microparticles derived from red blood cell units (RMPs). We incubated different colon carcinoma cells with RMPs and analyzed their effects on growth, invasion, migration and tumor marker expression. Furthermore, effects on Wnt, Akt and ERK signaling were explored. Our results show RMPs do not seem to affect functional and phenotypic characteristics of different colon carcinoma cells and did not induce or inhibit Wnt, Akt or ERK signaling, albeit in cell culture models lacking tumor microenvironment. Allogeneic blood transfusions are associated with poor prognosis, but RMPs do not seem to convey tumor-enhancing effects. Most likely, the circumstances that necessitate the transfusion, such as preoperative anemia, tumor stage, perioperative blood loss and extension of surgery, take center stage.

Indexed as

CarcinomaCell-Derived MicroparticlesColonic NeoplasmsHumansNeoplasm Recurrence, LocalProto-Oncogene Proteins c-aktRetrospective StudiesTumor MicroenvironmentProto-Oncogene Proteins c-aktcolorectal carcinomamicroparticlesred blood cellstransfusion

Identifiers

PMID36012587
PMCPMC9409112
OpenAlexW4293513516

What Socratic 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 Socratic graph.