Evidence map›Paper›PMID 37397521›Full record

ReviewGenes & diseases2023

Histone post-translational modification and the DNA damage response.

Haoyun Song, Rong Shen, Xiangwen Liu, Xuguang Yang, Kun Xie, Zhao Guo, Degui Wang

Abstract readReview
In one paragraph

Review in Genes & diseases, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
–field-weighted citation impact
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

27 citing papers in PubMed.

  1. Review
  2. Article
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  9. ACS omega · 2025
    Article
  10. Article
  11. Review
  12. Review
  13. Review
  14. Article
  15. Review
  16. Review
  17. Histone Phosphorylation in DNA Damage Response.International journal of molecular sciences · 2025
    Review
  18. Article
  19. Review
  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

7 authors.

Haoyun SongSchool of Basic Medical Sciences, Lanzhou University, Lanzhou, Gansu 730000, China.
Rong ShenSchool of Basic Medical Sciences, Lanzhou University, Lanzhou, Gansu 730000, China.
Xiangwen LiuSchool of Basic Medical Sciences, Lanzhou University, Lanzhou, Gansu 730000, China.
Xuguang YangSchool of Basic Medical Sciences, Lanzhou University, Lanzhou, Gansu 730000, China.
Kun XieSchool of Basic Medical Sciences, Lanzhou University, Lanzhou, Gansu 730000, China.
Zhao GuoSchool of Basic Medical Sciences, Lanzhou University, Lanzhou, Gansu 730000, China.
Degui WangSchool of Basic Medical Sciences, Lanzhou University, Lanzhou, Gansu 730000, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

DNA is highly vulnerable to spontaneous and environmental timely damage in living cells. DNA damage may cause genetic instability and increase cancer risk if the damages are not repaired timely and efficiently. Human cells possess several DNA damage response (DDR) mechanisms to protect the integrity of their genome. Clarification of the mechanisms underlying the DNA damage response following lethal damage will facilitate the identification of therapeutic targets for cancers. Histone post-translational modifications (PTMs) have been indicated to play different roles in the repair of DNA damage. In this context, histone PTMs regulate recruitment of downstream effectors, and facilitate appropriate repair response. This review outlines the current understanding of different histone PTMs in response to DNA damage repair, besides, enumerates the role of new type PTMs such as histone succinylation and crotonylation in regulating DNA damage repair processes.

Indexed as

DNA damageDNA damage responseHistonePost-translational modifications (PTMs)

Identifiers

PMID37397521
PMCPMC10310986

What OpenQuestion holds

Textmetadata
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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.