Evidence map›Paper›PMID 26184161›Full record

ReviewInternational journal of molecular sciences2015

Poly(ADP-Ribose) Polymerase 1: Cellular Pluripotency, Reprogramming, and Tumorogenesis.

Bo-Hua Jiang, Wei-Lien Tseng, Hsin-Yang Li, Mong-Lien Wang, Yuh-Lih Chang, Yen-Jen Sung, Shih-Hwa Chiou

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.4field-weighted citation impact, top 17% 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

23 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. NADMolecular and cellular biochemistry · 2022
    Review
  10. Article
  11. Review
  12. CanGynecologic oncology reports · 2021
    Article
  13. The role of Trop2 in prostate cancer: an oncogene, biomarker, and therapeutic target.American journal of clinical and experimental urology · 2021
    Article
  14. Article
  15. Trop2 is a driver of metastatic prostate cancer with neuroendocrine phenotype via PARP1.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  16. Article
  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

7 authors at 1 institution in 1 country.

Bo-Hua JiangInstitute of Oral Biology, National Yang-Ming University, Taipei 112, Taiwan. lovelace831124@yahoo.com.tw.
Wei-Lien TsengSchool of Medicine, National Yang-Ming University, Taipei 112, Taiwan. jan740709@gmail.com.
Hsin-Yang LiSchool of Medicine, National Yang-Ming University, Taipei 112, Taiwan. doc3643h@yahoo.com.tw.
Mong-Lien WangSchool of Medicine, National Yang-Ming University, Taipei 112, Taiwan. monglien@gmail.com.
Yuh-Lih ChangSchool of Medicine, National Yang-Ming University, Taipei 112, Taiwan. ylchang@vghtpe.gov.tw.
Yen-Jen SungSchool of Medicine, National Yang-Ming University, Taipei 112, Taiwan. yjsung@ym.edu.tw.
Shih-Hwa ChiouSchool of Medicine, National Yang-Ming University, Taipei 112, Taiwan. shchiou@vghtpe.gov.tw.
National Yang Ming Chiao Tung University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Poly(ADP-ribos)ylation (PARylation) is the catalytic function of the Poly(ADP-ribose) polymerases (Parps) family for post-translational modification in cellular process. Being a major member of Parps, Parp1 is a crucial nuclear factor with biological significance in modulating DNA repair, DNA replication, transcription, DNA methylation and chromatin remodeling through PARylation of downstream proteins. In addition, high expression level and activity of Parp1 are correlated with pluripotent status, reprogramming, and cancer. Furthermore, epigenetic modulation of Parp1 is explored for regulating wide variety of gene expression. Genetic and pharmaceutical disruption of Parp1 further confirmed the importance of Parp1 in cell growth, DNA repair, and reprogramming efficiency. Taken together, the proximity toward the understanding of the modulation of Parp1 including interaction and modification in different fields will provide new insight for future studies. In this review, the biological significance of Parp1 in transcription and the epigenetic modulation of Parp1 in pluripotent status, reprogramming process and cancer will be summarized.

Indexed as

CarcinogenesisCellular ReprogrammingChromatin Assembly and DisassemblyDNA MethylationDNA RepairHumansPoly(ADP-ribose) PolymerasesPoly(ADP-ribose) PolymerasesParp1PARylationpluripotencyreprogrammingtumorogenesis

Identifiers

PMID26184161
PMCPMC4519911
OpenAlexW1542520542

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.