Evidence map›Paper›PMID 38031977›Full record

ArticleInternational journal of immunopathology and pharmacology

Erastin induces ferroptosis in cervical cancer cells via Nrf2/HO-1 signaling pathway.

Xiaoning Wei, Qiaoqiao Huang, Jinbing Huang, Li Yu, Junying Chen

Open access · goldAbstract read
In one paragraph

Article in International journal of immunopathology and pharmacology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
7.2field-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

14 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Hypoxia Triggers ALYREF-Mediated mThe Kaohsiung journal of medical sciences · 2026
    Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Review
  13. Review
  14. Article
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 1 institution in 1 country.

Xiaoning WeiThe First Affiliated Hospital of Guangxi Medical University, Nanning, China.ORCID 0000-0002-2154-4117
Qiaoqiao HuangThe First Affiliated Hospital of Guangxi Medical University, Nanning, China.ORCID 0000-0003-0866-1594
Jinbing HuangThe First Affiliated Hospital of Guangxi Medical University, Nanning, China.ORCID 0009-0008-1006-6691
Li YuThe First Affiliated Hospital of Guangxi Medical University, Nanning, China.ORCID 0009-0006-1161-2688
Junying ChenThe First Affiliated Hospital of Guangxi Medical University, Nanning, China.ORCID 0000-0003-1969-9416
Guangxi Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveOur research aims to assess the influence of erastin, a ferroptosis-inducing agent, on cervical cancer cells.

introductionCervical cancer is a prevalent malignancy in females. Dysregulation of ferroptosis, a form of cell demise reliant on iron, is implicated in several cancers.

methodsThe effect of erastin on HeLa and SiHa was detected by transwell assay, scratch test, and colony formation assay, while cell apoptosis was detected using flow cytometry. Cellular reactive oxygen species (ROS) generation was detected using the dichloro-dihydro-fluorescein diacetate assay. Sequencing analysis identified differentially expressed genes (DEGs), and Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) Enrichment analyses were employed to identify the target gene. Subsequently, the utilization of small interfering RNA (siRNA) was employed to suppress the targeted gene expression in HeLa cells, thereby effectively mitigating the impact of erastin on various cellular processes including invasion, colony formation, migration, and ROS generation.

resultsThe findings indicate that erastin attenuates the viability of both HeLa cells (IC

conclusionOur research demonstrates that erastin induces ferroptosis and the accumulation of ROS in cervical cancer cells by activating the Nrf2/HO-1 pathway, significantly reducing cell proliferation and motility. These findings propose a potential molecular mechanism of erastin-mediated cervical cancer development.

Indexed as

FerroptosisUterine Cervical NeoplasmsFemaleHeLa CellsHeme Oxygenase-1HumansNF-E2-Related Factor 2PiperazinesReactive Oxygen SpeciesRNA, Small InterferingSignal TransductionerastinHeme Oxygenase-1NF-E2-Related Factor 2PiperazinesReactive Oxygen SpeciesRNA, Small Interferingcervical cancererastinferroptosisheme oxygenase-1Nrf2reactive oxygen species

Identifiers

PMID38031977
PMCPMC10687934
OpenAlexW4389180134

What Socratic holds

Textmetadata
LicenceCC BY-NC
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 Socratic graph.