Evidence map›Paper›PMID 31191665›Full record

ReviewStem cells international2019

The Best for the Most Important: Maintaining a Pristine Proteome in Stem and Progenitor Cells.

Bertal H Aktas, Berin Upcin, Erik Henke, Manju Padmasekar, Xuebin Qin, Süleyman Ergün

Open access · goldAbstract readReview
In one paragraph

Review in Stem cells international, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.1field-weighted citation impact, top 54% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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

6 authors at 3 institutions in 2 countries.

Bertal H AktasDivision of Hematology, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, 75 Francis Street, Boston, MA 02115, USA.ORCID 0000-0001-7829-4553
Berin UpcinInstitute of Anatomy and Cell Biology, Julius-Maximilians Universität Würzburg, Koellikerstrasse 6, Würzburg, 97070 Bayern, Germany.
Erik HenkeInstitute of Anatomy and Cell Biology, Julius-Maximilians Universität Würzburg, Koellikerstrasse 6, Würzburg, 97070 Bayern, Germany.ORCID 0000-0003-2380-2682
Manju PadmasekarInstitute of Anatomy and Cell Biology, Julius-Maximilians Universität Würzburg, Koellikerstrasse 6, Würzburg, 97070 Bayern, Germany.
Xuebin QinDepartment of Neurology, Temple University, Philadelphia, USA.
Süleyman ErgünInstitute of Anatomy and Cell Biology, Julius-Maximilians Universität Würzburg, Koellikerstrasse 6, Würzburg, 97070 Bayern, Germany.ORCID 0000-0002-2112-5377
University of Würzburg · DEBrigham and Women's Hospital · USTemple University · US

Funding

Targeting Endoplasmic Reticulum Stress Response for Cancer TherapyR01CA152312 · NCI · HARVARD MEDICAL SCHOOL · PI AKTAS, BERTAL H. · 2011 to 2015
$1.8M
NCI NIH HHS R01 CA152312
6 · The paper itself

Abstract

Pluripotent stem cells give rise to reproductively enabled offsprings by generating progressively lineage-restricted multipotent stem cells that would differentiate into lineage-committed stem and progenitor cells. These lineage-committed stem and progenitor cells give rise to all adult tissues and organs. Adult stem and progenitor cells are generated as part of the developmental program and play critical roles in tissue and organ maintenance and/or regeneration. The ability of pluripotent stem cells to self-renew, maintain pluripotency, and differentiate into a multicellular organism is highly dependent on sensing and integrating extracellular and extraorganismal cues. Proteins perform and integrate almost all cellular functions including signal transduction, regulation of gene expression, metabolism, and cell division and death. Therefore, maintenance of an appropriate mix of correctly folded proteins, a pristine proteome, is essential for proper stem cell function. The stem cells' proteome must be pristine because unfolded, misfolded, or otherwise damaged proteins would interfere with unlimited self-renewal, maintenance of pluripotency, differentiation into downstream lineages, and consequently with the development of properly functioning tissue and organs. Understanding how various stem cells generate and maintain a pristine proteome is therefore essential for exploiting their potential in regenerative medicine and possibly for the discovery of novel approaches for maintaining, propagating, and differentiating pluripotent, multipotent, and adult stem cells as well as induced pluripotent stem cells. In this review, we will summarize cellular networks used by various stem cells for generation and maintenance of a pristine proteome. We will also explore the coordination of these networks with one another and their integration with the gene regulatory and signaling networks.

Identifiers

PMID31191665
PMCPMC6525796
OpenAlexW2942532809

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.