Evidence map›Paper›PMID 24080338›Full record

ArticleCancer letters2014

Pro-survival and pro-growth effects of stress-induced nitric oxide in a prostate cancer photodynamic therapy model.

Reshma Bhowmick, Albert W Girotti

Open access · greenAbstract read
In one paragraph

Article in Cancer letters, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing 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

37 citing papers in PubMed, 1 synthesis or guideline pooled it, 65 citations in OpenAlex.

  1. Association between endothelial nitric oxide synthase 894G>T polymorphism and prostate cancer risk: a meta-analysis of literature studies.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2014
    Pooled it
  2. Photodynamic treatment of glioblastoma plus endothelial cell spheroid models: increased proliferative and migratory aggressiveness of surviving tumor cells due to iNOS/NO upregulation.Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology · 2026
    Article
  3. Review
  4. 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
  5. Review
  6. Production and Role of Nitric Oxide in Endometrial Cancer.Antioxidants (Basel, Switzerland) · 2025
    Review
  7. Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Review
  13. Review
  14. The Negative Impact of Cancer Cell Nitric Oxide on Photodynamic Therapy.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  15. Review
  16. Review
  17. Review
  18. Review
  19. Review
  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.

Reshma BhowmickDepartment of Biochemistry, Medical College of Wisconsin, Milwaukee, WI, USA. Electronic address: rbhowmic@gmail.com.
Albert W GirottiDepartment of Biochemistry, Medical College of Wisconsin, Milwaukee, WI, 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

We discovered recently that human breast cancer cells subjected to photodynamic therapy (PDT)-like oxidative stress localized in mitochondria rapidly upregulated nitric oxide synthase-2 (NOS2) and nitric oxide (NO), which increased resistance to apoptotic photokilling. In this study, we asked whether human prostate cancer PC-3 cells would exploit NOS2/NO similarly and, if so, how proliferation of surviving cells might be affected. Irradiation of photosensitized PC-3 cells resulted in a rapid (<1 h), robust (~12-fold), and prolonged (∼20 h) post-irradiation upregulation of NOS2. Caspase-3/7 activation and apoptosis were stimulated by NOS2 inhibitors and a NO scavenger, implying that induced NO was acting cytoprotectively. Cyclic GMP involvement was ruled out, whereas suppression of pro-apoptotic JNK and p38 MAPK activation was clearly implicated. Cells surviving photostress grew back ~2-times faster than controls. NOS2 inhibition prevented this and the large increase in cell cycle S-phase occupancy observed after irradiation. Thus, photostress upregulation of NOS/NO elicited both a pro-survival and pro-growth response, both of which could compromise clinical PDT efficacy unless suppressed, e.g. by pharmacological intervention with a NOS2 inhibitor.

Indexed as

ApoptosisCaspase 3Caspase 7Cell CycleCell Line, TumorCell ProliferationCell SurvivalEnzyme ActivationFree RadicalsHumansLightMaleMAP Kinase Signaling SystemNitric OxideNitric Oxide Synthase Type IIPhotochemotherapyCASP3 protein, humanCASP7 protein, humanCaspase 3Caspase 7Free RadicalsNitric OxideNitric Oxide Synthase Type IINOS2 protein, humanNitric oxideNitric oxide synthasePancreatic cancerPhotodynamic therapy

Identifiers

PMID24080338
PMCPMC3874260
OpenAlexW2126780194

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.