Evidence map›Paper›PMID 16462769›Full record

ArticleOncogene2006

Heme oxygenase-1 protects tumor cells against photodynamic therapy-mediated cytotoxicity.

D Nowis, M Legat, T Grzela, J Niderla, E Wilczek, G M Wilczynski, E Głodkowska, P Mrówka, T Issat, J Dulak and 9 more

Open access · greenAbstract read
In one paragraph

Article in Oncogene, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed
5.7field-weighted citation impact, top 3% 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

70 citing papers in PubMed, 184 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. Heme Oxygenase-1 and Its Role in Colorectal Cancer.Antioxidants (Basel, Switzerland) · 2023
    Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Role ofInternational journal of molecular sciences · 2021
    Article
  18. Immune Modulation by Inhibitors of the HO System.International journal of molecular sciences · 2020
    Review
  19. Article
  20. Article

10 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

19 authors at 4 institutions in 1 country.

D NowisDepartment of Immunology, Center of Biostructure Research, The Medical University of Warsaw, Warsaw, Poland.
M Legat
T Grzela
J Niderla
E Wilczek
G M Wilczynski
E Głodkowska
P Mrówka
T Issat
J Dulak
A Józkowicz
H Waś
M Adamek
A Wrzosek
S Nazarewski
M Makowski
T Stokłosa
M Jakóbisiak
J Gołab
Medical University of Warsaw · PLJagiellonian University · PLInstytut Biologii Doświadczalnej im. Marcelego Nenckiego · PLSilesian Center for Heart Disease · PL

Funding

Wellcome Trust 073974
6 · The paper itself

Abstract

Photodynamic therapy is a promising antitumor treatment modality approved for the management of both early and advanced tumors. The mechanisms of its antitumor action include generation of singlet oxygen and reactive oxygen species that directly damage tumor cells and tumor vasculature. A number of mechanisms seem to be involved in the protective responses to PDT that include activation of transcription factors, heat shock proteins, antioxidant enzymes and antiapoptotic pathways. Elucidation of these mechanisms might result in the design of more effective combination strategies to improve the antitumor efficacy of PDT. Using DNA microarray analysis to identify stress-related genes induced by Photofrin-mediated PDT in colon adenocarcinoma C-26 cells, we observed a marked induction of heme oxygenase-1 (HO-1). Induction of HO-1 with hemin or stable transfection of C-26 with a plasmid vector encoding HO-1 increased resistance of tumor cells to PDT-mediated cytotoxicity. On the other hand, zinc (II) protoporphyrin IX, an HO-1 inhibitor, markedly augmented PDT-mediated cytotoxicity towards C-26 and human ovarian carcinoma MDAH2774 cells. Neither bilirubin, biliverdin nor carbon monoxide, direct products of HO-1 catalysed heme degradation, was responsible for cytoprotection. Importantly, desferrioxamine, a potent iron chelator significantly potentiated cytotoxic effects of PDT. Altogether our results indicate that HO-1 is involved in an important protective mechanism against PDT-mediated phototoxicity and administration of HO-1 inhibitors might be an effective way to potentiate antitumor effectiveness of PDT.

Indexed as

AnimalsCarbon MonoxideChelating AgentsDihematoporphyrin EtherHemeHeme Oxygenase-1HumansIronMiceNeoplasmsOligonucleotide Array Sequence AnalysisOxygenPhotochemotherapyReactive Oxygen SpeciesCarbon MonoxideChelating AgentsDihematoporphyrin EtherHemeHeme Oxygenase-1IronOxygenReactive Oxygen Species

Identifiers

PMID16462769
PMCPMC1538962
OpenAlexW2025541083

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.