Evidence map›Paper›PMID 25526085›Full record

ReviewCell death and differentiation2015

Old, new and emerging functions of caspases.

S Shalini, L Dorstyn, S Dawar, S Kumar

Registry-linked trialOpen access · bronzeAbstract readReview
In one paragraph

Review in Cell death and differentiation, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06195371 (The Impact of CASP3 Gene in Chemoresistant Breast Cancer), which is not on this map. Cited by 606 papers.

0numbers the graph read from it
0cells of the map it votes in
606citing papers in PubMed
32.2field-weighted citation impact, top 1% 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.

NCT06195371 not yet recruitingnot on this mapstarted 2024, after this paper: background citation

The Impact of CASP3 Gene in Chemoresistant Breast Cancer

TypeobservationalSponsorGehad Salah El-Din shakerRan2024 to 2026Enrolled60ConditionsBreast Cancer
3 · Its place in the literature

Who cites it

606 citing papers in PubMed, 1,260 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Doxorubicin-Induced Cytotoxicity in Adipose-Derived Stem Cells Is Associated With Altered SAPK/JNK Signaling.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Statin-Associated Hepatotoxicity Linked toYonsei medical journal · 2026
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Programmed cell death of keratinocytes: an active driver in psoriasis.Apoptosis : an international journal on programmed cell death · 2026
    Review
  18. Article
  19. Article
  20. Article

546 more citing papers are in PubMed but not listed here.

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 2 institutions in 1 country.

S ShaliniCentre for Cancer Biology, University of South Australia, Adelaide, SA 5001, Australia.
L DorstynCentre for Cancer Biology, University of South Australia, Adelaide, SA 5001, Australia.
S DawarCentre for Cancer Biology, University of South Australia, Adelaide, SA 5001, Australia.
S KumarCentre for Cancer Biology, University of South Australia, Adelaide, SA 5001, Australia.
Centre for Cancer Biology · AUUniversity of South Australia · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Caspases are proteases with a well-defined role in apoptosis. However, increasing evidence indicates multiple functions of caspases outside apoptosis. Caspase-1 and caspase-11 have roles in inflammation and mediating inflammatory cell death by pyroptosis. Similarly, caspase-8 has dual role in cell death, mediating both receptor-mediated apoptosis and in its absence, necroptosis. Caspase-8 also functions in maintenance and homeostasis of the adult T-cell population. Caspase-3 has important roles in tissue differentiation, regeneration and neural development in ways that are distinct and do not involve any apoptotic activity. Several other caspases have demonstrated anti-tumor roles. Notable among them are caspase-2, -8 and -14. However, increased caspase-2 and -8 expression in certain types of tumor has also been linked to promoting tumorigenesis. Increased levels of caspase-3 in tumor cells causes apoptosis and secretion of paracrine factors that promotes compensatory proliferation in surrounding normal tissues, tumor cell repopulation and presents a barrier for effective therapeutic strategies. Besides this caspase-2 has emerged as a unique caspase with potential roles in maintaining genomic stability, metabolism, autophagy and aging. The present review focuses on some of these less studied and emerging functions of mammalian caspases.

Indexed as

AnimalsApoptosisCarcinogenesisCaspasesCell DifferentiationGenomic InstabilityHumansInflammation MediatorsRegenerationCaspasesInflammation Mediators

Identifiers

PMID25526085
PMCPMC4356345
OpenAlexW2016540525

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.