Evidence map›Paper›PMID 27221660›Full record

ReviewGenomics, proteomics & bioinformatics2016

DNA Damage Response in Hematopoietic Stem Cell Ageing.

Tangliang Li, Zhong-Wei Zhou, Zhenyu Ju, Zhao-Qi Wang

Open access · goldAbstract readReview
In one paragraph

Review in Genomics, proteomics & bioinformatics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

33 citing papers in PubMed, 63 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
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  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. The landscape of aging.Science China. Life sciences · 2022
    Review
  13. Hematopoietic Stem Cells and Regeneration.Cold Spring Harbor perspectives in biology · 2022
    Review
  14. DNA damage and repair in the hematopoietic system.Acta biochimica et biophysica Sinica · 2022
    Review
  15. Rg1 Protects Hematopoietic Stem Cells from LiCl-Induced Oxidative Stress via Wnt Signaling Pathway.Evidence-based complementary and alternative medicine : eCAM · 2022
    Article
  16. Hematopoiesis during Ontogenesis, Adult Life, and Aging.International journal of molecular sciences · 2021
    Review
  17. Article
  18. Article
  19. Article
  20. Article
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

4 authors at 2 institutions in 2 countries.

Tangliang LiInstitute of Aging Research, School of Medicine, Hangzhou Normal University, Hangzhou 311121, China. Electronic address: li.tangliang@hznu.edu.cn.
Zhong-Wei ZhouLeibniz Institute on Aging - Fritz Lipmann Institute (FLI), Jena D-07745, Germany.
Zhenyu JuInstitute of Aging Research, School of Medicine, Hangzhou Normal University, Hangzhou 311121, China.
Zhao-Qi WangLeibniz Institute on Aging - Fritz Lipmann Institute (FLI), Jena D-07745, Germany; Faculty of Biology and Pharmacy, Friedrich-Schiller University of Jena, Jena D-07745, Germany.
Hangzhou Normal University · CNLeibniz Institute on Aging - Fritz Lipmann Institute (FLI) · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Maintenance of tissue-specific stem cells is vital for organ homeostasis and organismal longevity. Hematopoietic stem cells (HSCs) are the most primitive cell type in the hematopoietic system. They divide asymmetrically and give rise to daughter cells with HSC identity (self-renewal) and progenitor progenies (differentiation), which further proliferate and differentiate into full hematopoietic lineages. Mammalian ageing process is accompanied with abnormalities in the HSC self-renewal and differentiation. Transcriptional changes and epigenetic modulations have been implicated as the key regulators in HSC ageing process. The DNA damage response (DDR) in the cells involves an orchestrated signaling pathway, consisting of cell cycle regulation, cell death and senescence, transcriptional regulation, as well as chromatin remodeling. Recent studies employing DNA repair-deficient mouse models indicate that DDR could intrinsically and extrinsically regulate HSC maintenance and play important roles in tissue homeostasis of the hematopoietic system. In this review, we summarize the current understanding of how the DDR determines the HSC fates and finally contributes to organismal ageing.

Indexed as

DNA RepairAnimalsCell Cycle CheckpointsCell Cycle ProteinsCell DifferentiationCellular SenescenceChromatin Assembly and DisassemblyDNA DamageHematopoietic Stem CellsSignal TransductionTumor Suppressor Protein p53Cell Cycle ProteinsTumor Suppressor Protein p53AgeingDNA damage responseEpigeneticsHematopoietic stem cellsP53

Identifiers

PMID27221660
PMCPMC4936660
OpenAlexW2407975629

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.