Evidence map›Paper›PMID 35628518›Full record

ArticleInternational journal of molecular sciences2022

Heme Oxygenase Modulation Drives Ferroptosis in TNBC Cells.

Valeria Consoli, Valeria Sorrenti, Valeria Pittalà, Khaled Greish, Agata Grazia D'Amico, Giuseppe Romeo, Sebastiano Intagliata, Loredana Salerno, Luca Vanella

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
7.3field-weighted citation impact, top 2% 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

33 citing papers in PubMed, 50 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Metabolic Regulation of Ferroptosis in Breast Cancer.International journal of molecular sciences · 2025
    Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Mitochondrial Regulation of Ferroptosis in Cancer Cells.International journal of biological sciences · 2025
    Review
  16. Article
  17. Article
  18. Glycyrol Alleviates Acute Kidney Injury by Inhibiting Ferroptsis.International journal of molecular sciences · 2024
    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

9 authors at 2 institutions in 2 countries.

Valeria ConsoliDepartment of Drug and Health Science, University of Catania, 95125 Catania, Italy.ORCID 0000-0001-8961-5818
Valeria SorrentiDepartment of Drug and Health Science, University of Catania, 95125 Catania, Italy.ORCID 0000-0002-5973-1495
Valeria PittalàDepartment of Drug and Health Science, University of Catania, 95125 Catania, Italy.ORCID 0000-0003-1856-0308
Khaled GreishPrincess Al-Jawhara Centre for Molecular Medicine, Department of Molecular Medicine, School of Medicine and Medical Sciences, Arabian Gulf University, Manama 329, Bahrain.ORCID 0000-0002-0787-7070
Agata Grazia D'AmicoDepartment of Drug and Health Science, University of Catania, 95125 Catania, Italy.
Giuseppe RomeoDepartment of Drug and Health Science, University of Catania, 95125 Catania, Italy.
Sebastiano IntagliataDepartment of Drug and Health Science, University of Catania, 95125 Catania, Italy.ORCID 0000-0002-0201-1745
Loredana SalernoDepartment of Drug and Health Science, University of Catania, 95125 Catania, Italy.ORCID 0000-0001-6458-3717
Luca VanellaDepartment of Drug and Health Science, University of Catania, 95125 Catania, Italy.ORCID 0000-0002-6314-6029
University of Catania · ITArabian Gulf University · BH

Funding

This work was founded by the University of Catania, Programma Ricerca di Ateneo Pia.Ce.Ri 2020-2022 linea 2 project number 57722172126
6 · The paper itself

Abstract

The term ferroptosis refers to a peculiar type of programmed cell death (PCD) mainly characterized by extensive iron-dependent lipid peroxidation. Recently, ferroptosis has been suggested as a potential new strategy for the treatment of several cancers, including breast cancer (BC). In particular, among the BC subtypes, triple negative breast cancer (TNBC) is considered the most aggressive, and conventional drugs fail to provide long-term efficacy. In this context, our study's purpose was to investigate the mechanism of ferroptosis in breast cancer cell lines and reveal the significance of heme oxygenase (HO) modulation in the process, providing new biochemical approaches. HO's effect on BC was evaluated by MTT tests, gene silencing, Western blot analysis, and measurement of reactive oxygen species (ROS), glutathione (GSH) and lipid hydroperoxide (LOOH) levels. In order to assess HO's implication, different approaches were exploited, using two distinct HO-1 inducers (hemin and curcumin), a well-known HO inhibitor (SnMP) and a selective HO-2 inhibitor. The data obtained showed HO's contribution to the onset of ferroptosis; in particular, HO-1 induction seemed to accelerate the process. Moreover, our results suggest a potential role of HO-2 in erastin-induced ferroptosis. In view of the above, HO modulation in ferroptosis can offer a novel approach for breast cancer treatment.

Indexed as

FerroptosisHeme Oxygenase (Decyclizing)Triple Negative Breast NeoplasmsGlutathioneHumansLipid PeroxidesReactive Oxygen SpeciesGlutathioneHeme Oxygenase (Decyclizing)Lipid PeroxidesReactive Oxygen SpeciescancercurcuminerastinhemeHO-1HO-2inducersinhibitors

Identifiers

PMID35628518
PMCPMC9143660
OpenAlexW4281637660

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.