Evidence map›Paper›PMID 19855190›Full record

ReviewAutophagy2010

Assessing autophagy in the context of photodynamic therapy.

John J Reiners, Patrizia Agostinis, Kristian Berg, Nancy L Oleinick, David Kessel

Open access · bronzeAbstract readEvaluation StudyReview
In one paragraph

Review in Autophagy, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 87 papers.

0numbers the graph read from it
0cells of the map it votes in
87citing papers in PubMed
11.1field-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.

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

87 citing papers in PubMed, 224 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Review
  6. Article
  7. Recent development of nanomaterials-based PDT to improve immunogenic cell death.Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology · 2024
    Review
  8. Cellular Mechanisms of Singlet Oxygen in Photodynamic Therapy.International journal of molecular sciences · 2023
    Review
  9. Article
  10. Photodynamic therapy reduces cell viability, migration and triggers necroptosis in prostate tumor cells.Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology · 2023
    Article
  11. Review
  12. Review
  13. Review
  14. Article
  15. Impact of mono- and di-β-galactose moieties inEuropean journal of medicinal chemistry reports · 2022
    Article
  16. Review
  17. Review
  18. Article
  19. Detection of Paraptosis After Photodynamic Therapy.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  20. Review

27 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

5 authors at 3 institutions in 3 countries.

John J ReinersInstitute of Environmental Health Sciences, Wayne State University, Detroit, MI, USA.
Patrizia Agostinis
Kristian Berg
Nancy L Oleinick
David Kessel
Wayne State University · USCase Western Reserve University · USKU Leuven · BE

Funding

RESEARCH CORE-- SIGNAL TRANSDUCTIONP30ES006639 · NIEHS · WAYNE STATE UNIVERSITY · PI DERESKI, MARY O · 1994 to 2008
$13.1M
Subcellular targets and PDT-induces cell deathR01CA023378 · NCI · WAYNE STATE UNIVERSITY · PI KESSEL, DAVID HARRY · 1985 to 2013
$3.3M
PHOTOTHERAPY OF PROSTATE CANCER--PRO AND ANTI APOPTOSISR01CA083917 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI OLEINICK, NANCY L · 2000 to 2006
$2.3M
Cardiolipin in Photodynamic TherapyR01CA106491 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI OLEINICK, NANCY L · 2005 to 2008
$972k
NCI NIH HHS CA 106491NCI NIH HHS CA23378NCI NIH HHS CA 83917NCI NIH HHS R01 CA023378NCI NIH HHS R01 CA083917NCI NIH HHS R01 CA106491NIEHS NIH HHS P30 ES006639NIEHS NIH HHS P30 ES06639
6 · The paper itself

Abstract

Photodynamic therapy (PDT) is a procedure that has applications in the selective eradication of neoplasia where sites of malignant lesions are clearly delineated. It is a two-step process whereby cells are first sensitized to light and then photoirradiated. This results in the formation of singlet molecular oxygen and other reactive oxygen species that can cause photodamage at sites where the photosensitizing agent has localized. Photosensitizers found to be clinically useful show affinity for the endoplasmic reticulum (ER), mitochondria, lysosomes, or combinations of these sites. The induction of apoptosis and/or autophagy in photosensitized cells is a common outcome of PDT. This report explores the following issues: (1) Does the induction of autophagy in PDT protocols occur independent of, or in association with, apoptosis? (2) Does the resulting autophagy play a prosurvival or prodeath role? (3) Do photosensitizers damage/inactivate specific proteins that are components of, or that modulate the autophagic process? (4) Can an autophagic response be mounted in cells in which lysosomes are specifically photodamaged? In brief, autophagy can occur independently of apoptosis in PDT protocols, and appears to play a prosurvival role in apoptosis competent cells, and a prodeath role in apoptosis incompetent cells. Mitochondrial and ER-localized sensitizers cause selective photodamage to some (i.e., Bcl-2, Bcl-x(L), mTOR) proteins involved in the apoptotic/autophagic process. Finally, an aborted autophagic response occurs in cells with photodamaged lysosomes. Whereas autophagosomes form, digestion of their cargo is compromised because of the absence of functional lysosomes.

Indexed as

PhotochemotherapyAnimalsAutophagybcl-2-Associated X Proteinbcl-2 Homologous Antagonist-Killer ProteinCell Line, TumorCell SurvivalGene Knockout TechniquesHeLa CellsHumansMiceModels, BiologicalNeoplasmsPrognosisbcl-2-Associated X Proteinbcl-2 Homologous Antagonist-Killer Protein

Identifiers

PMID19855190
PMCPMC2861993
OpenAlexW2044630250

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.