Evidence map›Paper›PMID 25594039›Full record

ReviewOncoscience2014

Necrosis, and then stress induced necrosis-like cell death, but not apoptosis, should be the preferred cell death mode for chemotherapy: clearance of a few misconceptions.

Ju Zhang, Xiaomin Lou, Longyu Jin, Rongjia Zhou, Siqi Liu, Ningzhi Xu, D Joshua Liao

Open access · hybridAbstract readReview
In one paragraph

Review in Oncoscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

28 citing papers in PubMed, 56 citations in OpenAlex.

  1. Review
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  3. Ferroptosis in Cancer: Mechanism and Therapeutic Potential.International journal of molecular sciences · 2025
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  5. Synthesis,RSC medicinal chemistry · 2024
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  7. Anticancer and Antioxidant Activity of Water-Soluble Polysaccharides fromInternational journal of molecular sciences · 2022
    Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Brown SeaweedMolecules (Basel, Switzerland) · 2019
    Article
  13. Article
  14. Review
  15. Review
  16. Review
  17. Review
  18. Anticancer Properties of Graviola (Oxidative medicine and cellular longevity · 2018
    Review
  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

7 authors at 6 institutions in 2 countries.

Ju ZhangCAS Key Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing, P.R. China.
Xiaomin LouCAS Key Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing, P.R. China.
Longyu JinHormel Institute, University of Minnesota, Austin, MN, USA.
Rongjia ZhouDepartment of Genetics & Center for Developmental Biology, College of Life Sciences, Wuhan University, Wuhan, P. R. China.
Siqi LiuCAS Key Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing, P.R. China.
Ningzhi XuLaboratory of Cell and Molecular Biology, Cancer Institute, Academy of Medical Science, Beijing, P.R. China.
D Joshua LiaoHormel Institute, University of Minnesota, Austin, MN, USA.
Beijing Institute of Genomics · CNChinese Academy of Medical Sciences & Peking Union Medical College · CNChinese Academy of Sciences · CNHormel (United States) · USUniversity of Minnesota · USWuhan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cell death overarches carcinogenesis and is a center of cancer researches, especially therapy studies. There have been many nomenclatures on cell death, but only three cell death modes are genuine, i.e. apoptosis, necrosis and stress-induced cell death (SICD). Like apoptosis, SICD is programmed. Like necrosis, SICD is a pathological event and may trigger regeneration and scar formation. Therefore, SICD has subtypes of stress-induced apoptosis-like cell death (SIaLCD) and stress-induced necrosis-like cell death (SInLCD). Whereas apoptosis removes redundant but healthy cells, SICD removes useful but ill or damaged cells. Many studies on cell death involve cancer tissues that resemble parasites in the host patients, which is a complicated system as it involves immune clearance of the alien cancer cells by the host. Cancer resembles an evolutionarily lower-level organism having a weaker apoptosis potential and poorer DNA repair mechanisms. Hence, targeting apoptosis for cancer therapy, i.e. killing via SIaLCD, will be less efficacious and more toxic. On the other hand, necrosis of cancer cells releases cellular debris and components to stimulate immune function, thus counteracting therapy-caused immune suppression and making necrosis better than SIaLCD for chemo drug development.

Indexed as

ApoptosisCancer therapyCarcinogenesisEvolutionHyperthermia

Identifiers

PMID25594039
PMCPMC4284620
OpenAlexW2142488944

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.