Evidence map›Paper›PMID 26798361›Full record

ReviewStem cells international2016

Peripheral Blood Monocytes as Adult Stem Cells: Molecular Characterization and Improvements in Culture Conditions to Enhance Stem Cell Features and Proliferative Potential.

Hendrik Ungefroren, Ayman Hyder, Maren Schulze, Karim M Fawzy El-Sayed, Evelin Grage-Griebenow, Andreas K Nussler, Fred Fändrich

Open access · goldAbstract readReview
In one paragraph

Review in Stem cells international, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

13 citing papers in PubMed, 29 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

7 authors at 5 institutions in 2 countries.

Hendrik UngefrorenFirst Department of Medicine, UKSH, Campus Lübeck, Ratzeburger Allee 160, 23538 Lübeck, Germany.
Ayman HyderClinic for Applied Cellular Medicine, UKSH, Campus Kiel, Arnold-Heller Strasse 3, Haus 18, 24105 Kiel, Germany; Faculty of Science, Damietta University, Damietta 34517, Egypt.
Maren SchulzeDepartment of General, Visceral and Transplantation Surgery, University Hospital Essen, Hufelandstrasse 55, 45147 Essen, Germany.
Karim M Fawzy El-SayedClinic for Conservative Dentistry and Periodontology, School of Dental Medicine, UKSH, Campus Kiel, Arnold-Heller Strasse 3, Haus 26, 24105 Kiel, Germany; Oral Medicine and Periodontology Department, Faculty of Oral and Dental Medicine, Cairo University, 1 Mathaf El Manial Street, Giza, Egypt.
Evelin Grage-GriebenowFirst Department of Medicine, UKSH, Campus Lübeck, Ratzeburger Allee 160, 23538 Lübeck, Germany.
Andreas K NusslerBG Unfallklinik Tübingen, Eberhard Karls Universität Tübingen, Schnarrenbergstraße 95, 72076 Tübingen, Germany.
Fred FändrichClinic for Applied Cellular Medicine, UKSH, Campus Kiel, Arnold-Heller Strasse 3, Haus 18, 24105 Kiel, Germany.
Universitäres Kinderwunschzentrum Lübeck · DEDamietta University · EGEssen University Hospital · DEKiel University · DEUniversity of Tübingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Adult stem or programmable cells hold great promise in diseases in which damaged or nonfunctional cells need to be replaced. We have recently demonstrated that peripheral blood monocytes can be differentiated in vitro into cells resembling specialized cell types like hepatocytes and pancreatic beta cells. During phenotypic conversion, the monocytes downregulate monocyte/macrophage differentiation markers, being indicative of partial dedifferentiation, and are partially reprogrammed to acquire a state of plasticity along with expression of various markers of pluripotency and resumption of mitosis. Upregulation of stem cell markers and mitotic activity in the cultures was shown to be controlled by autocrine production/secretion of activin A and transforming growth factor-beta (TGF-β). These reprogrammed monocyte derivatives were termed "programmable cells of monocytic origin" (PCMO). Current efforts focus on establishing culture conditions that increase both the plasticity and proliferation potential of PCMO in order to be able to generate large amounts of blood-derived cells suitable for both autologous and allogeneic therapies.

Identifiers

PMID26798361
PMCPMC4699085
OpenAlexW2257472842

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.