Evidence map›Paper›PMID 24974291›Full record

ReviewMethods in enzymology2014

Turning on caspases with genetics and small molecules.

Charles W Morgan, Olivier Julien, Elizabeth K Unger, Nirao M Shah, James A Wells

Open access · greenAbstract readReview
In one paragraph

Review in Methods in enzymology, 2014. 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
3.5field-weighted citation impact, top 8% 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, 33 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Evaluation of Caspase-3 Activity During Apoptosis with Fluorescence Lifetime-Based Cytometry Measurements and Phasor Analyses.Cytometry. Part A : the journal of the International Society for Analytical Cytology · 2020
    Article
  7. Article
  8. Article
  9. Adeno-Associated Viral Vectors in Neuroscience Research.Molecular therapy. Methods & clinical development · 2020
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Genetic dissection of neural circuits underlying sexually dimorphic social behaviours.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2016
    Review
  16. Article
  17. Article
  18. Article
  19. Article
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

5 authors at 1 institution in 1 country.

Charles W MorganDepartment of Pharmaceutical Chemistry, University of California, San Francisco, California, USA; Graduate Group in Chemistry and Chemical Biology, University of California, San Francisco, California, USA.
Olivier JulienDepartment of Pharmaceutical Chemistry, University of California, San Francisco, California, USA.
Elizabeth K UngerDepartment of Anatomy, University of California, San Francisco, California, USA; Program in Biomedical Sciences, University of California, San Francisco, California, USA.
Nirao M ShahDepartment of Anatomy, University of California, San Francisco, California, USA. Electronic address: nms@ucsf.edu.
James A WellsDepartment of Pharmaceutical Chemistry, University of California, San Francisco, California, USA; Department of Cellular and Molecular Pharmacology, University of California, San Francisco, California, USA. Electronic address: jim.wells@ucsf.edu.
University of California, San Francisco · US

Funding

Characterization of Sexual Dimorphism in the BrainR01NS049488 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Nirao Mahesh Shah · 2005 to 2026
$8.7M
RESEARCH TRAINING IN CHEMISTRY AND CHEMICAL BIOLOGYT32GM064337 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CRAIK, CHARLES SCOTT · 2002 to 2021
$7.8M
Global Analysis of Proteolysis in ApoptosisR01GM081051 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI WELLS, JAMES A · 2007 to 2015
$2.8M
Dissecting hypothalamic pathways that regulate sexually dimorphic behaviorsR01NS083872 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI SHAH, NIRAO MAHESH · 2013 to 2017
$1.8M
Direct Chemical Activators of CaspasesR01CA136779 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI WELLS, JAMES A · 2009 to 2013
$1.5M
Dissecting the neural control of social attachmentDP1MH099900 · NIMH · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI SHAH, NIRAO MAHESH · 2012 to 2013
$1.5M
Characterizing the role of the medial amygdala in sexually dimorphic behaviorsF31NS078959 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI UNGER, ELIZABETH K. · 2012 to 2014
$108k
NCCDPHP CDC HHS DP1MH099900NCI NIH HHS R01 CA136779NIGMS NIH HHS R01 GM081051NIGMS NIH HHS T32 GM064337NIMH NIH HHS DP1 MH099900NINDS NIH HHS F31 NS078959NINDS NIH HHS R01 NS049488NINDS NIH HHS R01NS049488NINDS NIH HHS R01 NS083872NINDS NIH HHS R01NS083872
6 · The paper itself

Abstract

Caspases, aspartate-specific cysteine proteases, have fate-determining roles in many cellular processes including apoptosis, differentiation, neuronal remodeling, and inflammation (for review, see Yuan & Kroemer, 2010). There are a dozen caspases in humans alone, yet their individual contributions toward these phenotypes are not well understood. Thus, there has been considerable interest in activating individual caspases or using their activity to drive these processes in cells and animals. We envision that such experimental control of caspase activity can not only afford novel insights into fundamental biological problems but may also enable new models for disease and suggest possible routes to therapeutic intervention. In particular, localized, genetic, and small-molecule-controlled caspase activation has the potential to target the desired cell type in a tissue. Suppression of caspase activation is one of the hallmarks of cancer and thus there has been significant enthusiasm for generating selective small-molecule activators that could bypass upstream mutational events that prevent apoptosis. Here, we provide a practical guide that investigators have devised, using genetics or small molecules, to activate specific caspases in cells or animals. Additionally, we show genetically controlled activation of an executioner caspase to target the function of a defined group of neurons in the adult mammalian brain.

Indexed as

AnimalsApoptosisCaspasesCell EngineeringCloning, MolecularEnzyme ActivationHumansModels, MolecularNeuronsProtein MultimerizationSmall Molecule LibrariesCaspasesSmall Molecule LibrariesActivationAggressionApoptosisCaspaseCell deathCre-LoxProteaseSexual BehaviorSNIPerVentromedial HypothalamusVMHvl

Identifiers

PMID24974291
PMCPMC4249682
OpenAlexW151193486

What OpenQuestion holds

Textmetadata
LicenceTDM
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.