Evidence map›Paper›PMID 26068242›Full record

ArticleNitric oxide : biology and chemistry2015

Accelerated migration and invasion of prostate cancer cells after a photodynamic therapy-like challenge: Role of nitric oxide.

Jonathan M Fahey, Albert W Girotti

Abstract read
In one paragraph

Article in Nitric oxide : biology and chemistry, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 1 pooled it
5.0field-weighted citation impact, top 4% 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

45 citing papers in PubMed, 1 synthesis or guideline pooled it, 77 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Pro-tumor effects of nitric oxide from stress-upregulated inducible nitric oxide synthase in anti-tumor photodynamic therapy.Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology · 2025
    Review
  4. Integrin α6 Targeted Tumor Theranostics.Phenomics (Cham, Switzerland) · 2025
    Review
  5. Review
  6. Production and Role of Nitric Oxide in Endometrial Cancer.Antioxidants (Basel, Switzerland) · 2025
    Review
  7. Review
  8. Determinants of Photodynamic Therapy Resistance in Cancer Cells.International journal of molecular sciences · 2024
    Review
  9. Review
  10. Article
  11. Review
  12. Review
  13. Review
  14. 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
  15. Review
  16. Review
  17. Review
  18. The Negative Impact of Cancer Cell Nitric Oxide on Photodynamic Therapy.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  19. Article
  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

2 authors at 1 institution in 1 country.

Jonathan M FaheyDepartment of Biochemistry, Medical College of Wisconsin, Milwaukee, WI 53226-3548, USA.
Albert W GirottiDepartment of Biochemistry, Medical College of Wisconsin, Milwaukee, WI 53226-3548, USA. Electronic address: agirotti@mcw.edu.
Medical College of Wisconsin · US

Funding

IRON, NO, AND LIPID PEROXIDES IN PHOTODYNAMIC THERAPYR01CA070823 · NCI · MEDICAL COLLEGE OF WISCONSIN · PI GIROTTI, ALBERT · 1997 to 2015
$3.5M
IRON, NO, AND LIPID PEROXIDES IN PHOTODYNAMIC THERAPYR55CA070823 · NCI · MEDICAL COLLEGE OF WISCONSIN · PI GIROTTI, ALBERT W · 1996 to 1996
–
NCI NIH HHS CA70823NCI NIH HHS R01 CA070823
6 · The paper itself

Abstract

Employing an in vitro model for 5-aminolevulinic acid (ALA)-based photodynamic therapy (PDT), we recently reported that human prostate cancer PC3 cells rapidly and persistently overexpressed inducible nitric oxide synthase (iNOS) and nitric oxide (NO) after a moderate ALA/light challenge. The upregulated iNOS/NO was shown to play a key role in cell resistance to apoptotic photokilling and also in the dramatic growth spurt observed in surviving cells. In the present study, we found that PC3 cells surviving an ALA/light insult not only proliferated faster than non-stressed controls, but migrated and invaded faster as well, these effects being abrogated by an iNOS inhibitor or NO scavenger. Photostressed prostate DU145 cells exhibited similar behavior. Using in-gel zymography, we showed that PC3 extracellular matrix metalloproteinase-9 (MMP-9) was strongly activated 24 h after ALA/light treatment and that MMP-9 inhibitor TIMP-1 was downregulated, consistent with MMP-9 involvement in enhanced invasiveness. We also observed a photostress-induced upregulation of α6 and β1 integrins, implying their involvement as well. The MMP-9, TIMP-1, and integrin effects were strongly attenuated by iNOS inhibition, confirming NO's role in photostress-enhanced migration/invasion. This study reveals novel, potentially tumor-promoting, side-effects of prostate cancer PDT which may be averted through use of iNOS inhibitors as PDT adjuvants.

Indexed as

PhotochemotherapyCell Line, TumorCell MovementHumansMaleNeoplasm InvasivenessNitric OxideNitric Oxide Synthase Type IIPhotosensitizing AgentsProstatic NeoplasmsProtoporphyrinsUp-RegulationNitric OxideNitric Oxide Synthase Type IINOS2 protein, humanPhotosensitizing Agentsprotoporphyrin IXProtoporphyrinsCell migration/invasionNitric oxidePhotodynamic therapyProstate cancer

Identifiers

PMID26068242
PMCPMC4545398
OpenAlexW619017962

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.