Evidence map›Paper›PMID 36077699›Full record

ReviewCancers2022

PARP1: Liaison of Chromatin Remodeling and Transcription.

Wen Zong, Yamin Gong, Wenli Sun, Tangliang Li, Zhao-Qi Wang

Open access · goldAbstract readReview
In one paragraph

Review in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
7.3field-weighted citation impact, top 2% 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

50 citing papers in PubMed, 74 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. 18β-Glycyrrhetinic Acid AttenuatesAnimals : an open access journal from MDPI · 2026
    Article
  5. Article
  6. PARP1 Exhibits an Enzymatically Inactive Chromatin Binding Mode.bioRxiv : the preprint server for biology · 2026
    Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Review
  18. Article
  19. Review
  20. Review
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

5 authors at 3 institutions in 2 countries.

Wen ZongState Key Laboratory of Microbial Technology, Shandong University, Qingdao 266237, China.ORCID 0000-0001-7800-128X
Yamin GongLeibniz Institute on Aging-Fritz Lipmann Institute (FLI), 07745 Jena, Germany.
Wenli SunState Key Laboratory of Microbial Technology, Shandong University, Qingdao 266237, China.
Tangliang LiState Key Laboratory of Microbial Technology, Shandong University, Qingdao 266237, China.ORCID 0000-0003-0671-9166
Zhao-Qi WangLeibniz Institute on Aging-Fritz Lipmann Institute (FLI), 07745 Jena, Germany.ORCID 0000-0002-8336-3485
Shandong University · CNLeibniz Institute on Aging - Fritz Lipmann Institute (FLI) · DEShenzhen University · CN

Funding

CSRD VA 1Deutsche Forschungsgemeinschaft WA2627/11-1
6 · The paper itself

Abstract

Poly(ADP-ribosyl)ation (PARylation) is a covalent post-translational modification and plays a key role in the immediate response of cells to stress signals. Poly(ADP-ribose) polymerase 1 (PARP1), the founding member of the PARP superfamily, synthesizes long and branched polymers of ADP-ribose (PAR) onto acceptor proteins, thereby modulating their function and their local surrounding. PARP1 is the most prominent of the PARPs and is responsible for the production of about 90% of PAR in the cell. Therefore, PARP1 and PARylation play a pleotropic role in a wide range of cellular processes, such as DNA repair and genomic stability, cell death, chromatin remodeling, inflammatory response and gene transcription. PARP1 has DNA-binding and catalytic activities that are important for DNA repair, yet also modulate chromatin conformation and gene transcription, which can be independent of DNA damage response. PARP1 and PARylation homeostasis have also been implicated in multiple diseases, including inflammation, stroke, diabetes and cancer. Studies of the molecular action and biological function of PARP1 and PARylation provide a basis for the development of pharmaceutic strategies for clinical applications. This review focuses primarily on the role of PARP1 in the regulation of chromatin remodeling and transcriptional activation.

Indexed as

chromatininflammatory responsePARP1PARylationtranscription

Identifiers

PMID36077699
PMCPMC9454564
OpenAlexW4293659397

What Socratic 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 Socratic graph.