Evidence map›Paper›PMID 29435221›Full record

ReviewCell & bioscience2018

There are only four basic modes of cell death, although there are many ad-hoc variants adapted to different situations.

Xingde Liu, Wenxiu Yang, Zhizhong Guan, Wenfeng Yu, Bin Fan, Ningzhi Xu, D Joshua Liao

Open access · goldAbstract readReview
In one paragraph

Review in Cell & bioscience, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

29 citing papers in PubMed, 66 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. AIM2 sensors mediate immunity toProceedings of the National Academy of Sciences of the United States of America · 2023
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  9. Anticancer and Antioxidant Activity of Water-Soluble Polysaccharides fromInternational journal of molecular sciences · 2022
    Article
  10. Article
  11. The Apoptosis Paradox in Cancer.International journal of molecular sciences · 2022
    Review
  12. A century of programmed cell death in the ovary: a commentary.Journal of assisted reproduction and genetics · 2022
    Article
  13. Review
  14. Article
  15. Review
  16. Co-Targeting Plk1 and DNMT3a in Advanced Prostate Cancer.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2021
    Article
  17. Review
  18. Review
  19. Cytotoxicity, Antimicrobial, andFrontiers in chemistry · 2021
    Article
  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

7 authors at 3 institutions in 1 country.

Xingde Liu1Department of Cardiology, Guizhou Medical University Hospital, Guiyang, 550004 Guizhou People's Republic of China.
Wenxiu Yang2Department of Pathology, Guizhou Medical University Hospital, Guiyang, 550004 Guizhou People's Republic of China.
Zhizhong Guan3Key Lab of Endemic and Ethnic Diseases of the Ministry of Education of China in Guizhou Medical University, Guiyang, 550004 People's Republic of China.
Wenfeng Yu3Key Lab of Endemic and Ethnic Diseases of the Ministry of Education of China in Guizhou Medical University, Guiyang, 550004 People's Republic of China.
Bin Fan2Department of Pathology, Guizhou Medical University Hospital, Guiyang, 550004 Guizhou People's Republic of China.
Ningzhi Xu4Laboratory of Cell and Molecular Biology & State Key Laboratory of Molecular Oncology, National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, People's Republic of China.
D Joshua Liao2Department of Pathology, Guizhou Medical University Hospital, Guiyang, 550004 Guizhou People's Republic of China.
Guiyang Medical University · CNAffiliated Hospital of Guizhou Medical University · CNChinese Academy of Medical Sciences & Peking Union Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There have been enough cell death modes delineated in the biomedical literature to befuddle all cell death researchers. Mulling over cell death from the viewpoints of the host tissue or organ and of the host animal, we construe that there should be only two physiological cell death modes, i.e. apoptosis and senescent death (SD), as well as two pathological modes, i.e. necrosis and stress-induced cell death (SICD). Other death modes described in the literature are ad-hoc variants or coalescences of some of these four basic ones in different physiological or pathological situations. SD, SICD and necrosis kill useful cells and will thus trigger regeneration, wound healing and probably also scar formation. SICD and necrosis will likely instigate inflammation as well. Apoptosis occurs as a mechanism to purge no-longer useful cells from a tissue via phagocytosis by cells with phagocytic ability that are collectively tagged by us as scavengers, including macrophages; therefore apoptosis is not followed by regeneration and inflammation. The answer for the question of "who dies" clearly differentiates apoptosis from SD, SICD and necrosis, despite other similarities and disparities among the four demise modes. Apoptosis cannot occur in cell lines in vitro, because cell lines are immortalized by reprogramming the death program of the parental cells, because in culture there lack scavengers and complex communications among different cell types, and because culture condition is a stress to the cells. Several issues of cell death that remain enigmatic to us are also described for peers to deliberate and debate.

Indexed as

ApoptosisInflammationNecrosisProgrammed cell deathRegenerationScarSenescenceStress induced cell death

Identifiers

PMID29435221
PMCPMC5796572
OpenAlexW2796558327

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.