Evidence map›Paper›PMID 31866779›Full record

ReviewThe Yale journal of biology and medicine2019

Cell Cycle Proteins as Key Regulators of Postmitotic Cell Death.

Peng Xia, Yuening Liu, Jingrui Chen, Zhaokang Cheng

Abstract readReview
In one paragraph

Review in The Yale journal of biology and medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.1field-weighted citation impact, top 19% 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

19 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. JACC. CardioOncology · 2023
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. 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

4 authors at 1 institution in 1 country.

Peng XiaDepartment of Pharmaceutical Sciences, Washington State University, Spokane, WA.
Yuening LiuDepartment of Pharmaceutical Sciences, Washington State University, Spokane, WA.
Jingrui ChenDepartment of Pharmaceutical Sciences, Washington State University, Spokane, WA.
Zhaokang ChengDepartment of Pharmaceutical Sciences, Washington State University, Spokane, WA.
Washington State University Spokane · US

Funding

Promoting chemoresistance in the heartR00HL119605 · NHLBI · WASHINGTON STATE UNIVERSITY · PI CHENG, ZHAOKANG · 2016 to 2018
$747k
Mechanisms of cardiac chemosensitivityR56HL145034 · NHLBI · WASHINGTON STATE UNIVERSITY · PI CHENG, ZHAOKANG · 2019 to 2019
$449k
NHLBI NIH HHS R00 HL119605NHLBI NIH HHS R56 HL145034
6 · The paper itself

Abstract

Cell cycle progression in dividing cells, characterized by faithful replication of the genomic materials and duplication of the original cell, is fundamental for growth and reproduction of all mammalian organisms. Functional maturation of postmitotic cells, however, requires cell cycle exit and terminal differentiation. In mature postmitotic cells, many cell cycle proteins remain to be expressed, or can be induced and reactivated in pathological conditions such as traumatic injury and degenerative diseases. Interestingly, elevated levels of cell cycle proteins in postmitotic cells often do not induce proliferation, but result in aberrant cell cycle reentry and cell death. At present, the cell cycle machinery is known predominantly for regulating cell cycle progression and cell proliferation, albeit accumulating evidence indicates that cell cycle proteins may also control cell death, especially in postmitotic tissues. Herein, we provide a brief summary of these findings and hope to highlight the connection between cell cycle reentry and postmitotic cell death. In addition, we also outline the signaling pathways that have been identified in cell cycle-related cell death. Advanced understanding of the molecular mechanisms underlying cell cycle-related death is of paramount importance because this knowledge can be applied to develop protective strategies against pathologies in postmitotic tissues. Moreover, a full-scope understanding of the cell cycle machinery will allow fine tuning to favor cell proliferation over cell death, thereby potentially promoting tissue regeneration.

Indexed as

ApoptosisMitosisAnimalsCell Cycle ProteinsHumansMyocytes, CardiacNeuronsCell Cycle Proteinsapoptosiscardiomyocytecell cyclediseaseneuron

Identifiers

PMID31866779
PMCPMC6913832
OpenAlexW2997369060

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.