Evidence map›Paper›PMID 30655609›Full record

ReviewNature reviews. Molecular cell biology2019

Regulation of apoptosis in health and disease: the balancing act of BCL-2 family proteins.

Rumani Singh, Anthony Letai, Kristopher Sarosiek

Abstract readReview
In one paragraph

Review in Nature reviews. Molecular cell biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1,128 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1,128citing papers in PubMed, 3 pooled it
–field-weighted citation impact
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

1,128 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. The role of vitamin D signalling in β cell apoptosis: a systematic review.Apoptosis : an international journal on programmed cell death · 2026
    Pooled it
  2. Pooled it
  3. Pooled it
  4. Trial
  5. Article
  6. Review
  7. Triorganotin compounds as emerging nuclear retinoid X receptor ligands and their implications in cancer.Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine · 2026
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. B cells in cancer: functions, mechanisms and therapeutic advances.Signal transduction and targeted therapy · 2026
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. A safety pin against BAX.Nature chemical biology · 2026
    Article
  19. Review
  20. Article

1,068 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

3 authors.

Rumani SinghJohn B. Little Center for Radiation Sciences, Harvard T. H. Chan School of Public Health, Boston, MA, USA.
Anthony LetaiLab for Systems Pharmacology, Harvard Medical School, Boston, MA, USA. Anthony_Letai@dfci.harvard.edu.ORCID http://orcid.org/0000-0002-1993-9013
Kristopher SarosiekJohn B. Little Center for Radiation Sciences, Harvard T. H. Chan School of Public Health, Boston, MA, USA. sarosiek@hsph.harvard.edu.ORCID http://orcid.org/0000-0002-4618-5085

Funding

ProteomicsP01CA206978 · NCI · DANA-FARBER CANCER INST · PI WU, CATHERINE JU-YING · 2016 to 2025
$17.0M
Developmental regulation of apoptosis as a modifiable driver of radiotherapy-induced neurocognitive impairment in pediatric patientsR37CA248565 · NCI · HARVARD UNIVERSITY D/B/A HARVARD SCHOOL OF PUBLIC HEALTH · PI Kristopher Andrew Sarosiek · 2020 to 2026
$2.6M
Regulation of Apoptotic Priming and Competence in Healthy and Cancerous CellsR00CA188679 · NCI · HARVARD SCHOOL OF PUBLIC HEALTH · PI SAROSIEK, KRISTOPHER ANDREW · 2017 to 2019
$747k
Regulation of apoptotic priming and competence in healthy and cancerous cellsK99CA188679 · NCI · DANA-FARBER CANCER INST · PI SAROSIEK, KRISTOPHER ANDREW · 2014 to 2015
$178k
NCI NIH HHS K99 CA188679NCI NIH HHS P01 CA206978NCI NIH HHS R00 CA188679NCI NIH HHS R37 CA248565
6 · The paper itself

Abstract

The loss of vital cells within healthy tissues contributes to the development, progression and treatment outcomes of many human disorders, including neurological and infectious diseases as well as environmental and medical toxicities. Conversely, the abnormal survival and accumulation of damaged or superfluous cells drive prominent human pathologies such as cancers and autoimmune diseases. Apoptosis is an evolutionarily conserved cell death pathway that is responsible for the programmed culling of cells during normal eukaryotic development and maintenance of organismal homeostasis. This pathway is controlled by the BCL-2 family of proteins, which contains both pro-apoptotic and pro-survival members that balance the decision between cellular life and death. Recent insights into the dynamic interactions between BCL-2 family proteins and how they control apoptotic cell death in healthy and diseased cells have uncovered novel opportunities for therapeutic intervention. Importantly, the development of both positive and negative small-molecule modulators of apoptosis is now enabling researchers to translate the discoveries that have been made in the laboratory into clinical practice to positively impact human health.

Indexed as

AnimalsApoptosisDiseaseHomeostasisHumansNeoplasmsPathologyProto-Oncogene Proteins c-bcl-2Proto-Oncogene Proteins c-bcl-2

Identifiers

PMID30655609
PMCPMC7325303

What OpenQuestion holds

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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.