Evidence map›Paper›PMID 34639148›Full record

ArticleInternational journal of molecular sciences2021

Differential Marker Expression between Keratinocyte Stem Cells and Their Progeny Generated from a Single Colony.

Dema Ali, Dana Alhattab, Hanan Jafar, Malak Alzubide, Nour Sharar, Salwa Bdour, Abdalla Awidi

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 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.5field-weighted citation impact, top 33% 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

7 citing papers in PubMed, 5 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 2 institutions in 2 countries.

Dema AliCell Therapy Center, The University of Jordan, Amman 11942, Jordan.
Dana AlhattabCell Therapy Center, The University of Jordan, Amman 11942, Jordan.
Hanan JafarCell Therapy Center, The University of Jordan, Amman 11942, Jordan.
Malak AlzubideCell Therapy Center, The University of Jordan, Amman 11942, Jordan.
Nour ShararCell Therapy Center, The University of Jordan, Amman 11942, Jordan.
Salwa BdourDepartment of Clinical Laboratory Sciences, Faculty of Science, The University of Jordan, Amman 11942, Jordan.
Abdalla AwidiCell Therapy Center, The University of Jordan, Amman 11942, Jordan.
University of Jordan · JOKing Abdullah University of Science and Technology · SA

Funding

Scientific Research Fund/Ministry of Higher Education, Amman, Jordan MPH/1/41/2015
6 · The paper itself

Abstract

The stemness in keratinocyte stem cells (KSCs) is determined by their gene expression patterns. KSCs are crucial in maintaining epidermal homeostasis and wound repair and are widely used candidates for therapeutic applications. Although several studies have reported their positive identifiers, unique biomarkers for KSCs remain elusive. Here, we aim to identify potential candidate stem cell markers. Human epidermal keratinocytes (HEKs) from neonatal foreskin tissues were isolated and cultured. Single-cell clonal analysis identified and characterized three types of cells: KSCs (holoclones), transient amplifying cells (TACs; meroclones), and differentiated cells (DSCs; paraclones). The clonogenic potential of KSCs demonstrated the highest proliferation potential of KSCs, followed by TACs and DSCs, respectively. Whole-transcriptome analysis using microarray technology unraveled the molecular signatures of these cells. These results were validated by quantitative real-time polymerase chain reaction and flow cytometry analysis. A total of 301 signature upregulated and 149 downregulated differentially expressed genes (DEGs) were identified in the KSCs, compared to TACs and DSCs. Furthermore, DEG analyses revealed new sets of genes related to cell proliferation, cell adhesion, surface makers, and regulatory factors. In conclusion, this study provides a useful source of information for the identification of potential SC-specific candidate markers.

Indexed as

Gene Expression RegulationBiomarkersCell DifferentiationCells, CulturedClone CellsEpidermal CellsGene Expression ProfilingHumansKeratinocytesStem CellsBiomarkersdifferentiated cellsholoclonekeratinocyte stem cellsmerocloneparaclonestem cellstransit amplifying cells

Identifiers

PMID34639148
PMCPMC8509450
OpenAlexW3204192371

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.