Evidence map›Paper›PMID 38203758›Full record

ReviewInternational journal of molecular sciences2024

Role of SLC7A11/xCT in Ovarian Cancer.

Sonia Fantone, Federica Piani, Fabiola Olivieri, Maria Rita Rippo, Angelo Sirico, Nicoletta Di Simone, Daniela Marzioni, Giovanni Tossetta

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 71 papers.

0numbers the graph read from it
0cells of the map it votes in
71citing papers in PubMed
23.7field-weighted citation impact, top 1% 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

71 citing papers in PubMed, 84 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. [Role of programmed cell death in platinum resistance in ovarian cancer].Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2026
    Review
  7. Article
  8. Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Stress Granules: Novel Regulators of Programmed Cell Death.Mini reviews in medicinal chemistry · 2026
    Review
  16. Article
  17. Review
  18. High Co-Expression ofBiomedicines · 2025
    Article
  19. Review
  20. Article

11 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

8 authors at 5 institutions in 1 country.

Sonia FantoneScientific Direction, IRCCS INRCA, 60124 Ancona, Italy.
Federica PianiHypertension and Cardiovascular Risk Research Center, Medical and Surgical Sciences Department, Alma Mater Studiorum University of Bologna, 40126 Bologna, Italy.
Fabiola OlivieriScientific Direction, IRCCS INRCA, 60124 Ancona, Italy.
Maria Rita RippoDepartment of Clinical and Molecular Sciences, DISCLIMO, Università Politecnica delle Marche, 60126 Ancona, Italy.ORCID 0000-0003-3024-3495
Angelo SiricoObstetrics and Gynecology Unit, Sant'Anna e San Sebastiano Hospital, 81100 Caserta, Italy.
Nicoletta Di SimoneDepartment of Biomedical Sciences, Humanitas University, 20072 Milan, Italy.ORCID 0000-0003-1273-3335
Daniela MarzioniDepartment of Experimental and Clinical Medicine, Università Politecnica delle Marche, 60126 Ancona, Italy.ORCID 0000-0002-2267-0270
Giovanni TossettaDepartment of Experimental and Clinical Medicine, Università Politecnica delle Marche, 60126 Ancona, Italy.ORCID 0000-0001-7003-1230
Marche Polytechnic University · ITHumanitas University · ITIstituti di Ricovero e Cura a Carattere Scientifico · ITOspedale Sant'Anna · ITUniversity of Bologna · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ovarian cancer is one of the most dangerous gynecologic cancers worldwide and has a high fatality rate due to diagnosis at an advanced stage of the disease as well as a high recurrence rate due to the occurrence of chemotherapy resistance. In fact, chemoresistance weakens the therapeutic effects, worsening the outcome of this pathology. Solute Carrier Family 7 Member 11 (SLC7A11, also known as xCT) is the functional subunit of the Xc- system, an anionic L-cystine/L-glutamate antiporter expressed on the cell surface. SLC7A11 expression is significantly upregulated in several types of cancers in which it can inhibit ferroptosis and favor cancer cell proliferation, invasion and chemoresistance. SLC7A11 expression is also increased in ovarian cancer tissues, suggesting a possible role of this protein as a therapeutic target. In this review, we provide an overview of the current literature regarding the role of SLC7A11 in ovarian cancer to provide new insights on SLC7A11 modulation and evaluate the potential role of SLC7A11 as a therapeutic target.

Indexed as

Genital Neoplasms, FemaleOvarian NeoplasmsAmino Acid Transport System y+AntiportersCell MembraneFemaleGlutamic AcidHumansAmino Acid Transport System y+AntiportersGlutamic AcidSLC7A11 protein, humanchemoresistancecompoundsnon-coding RNAsnuclear factor erythroid 2-related factor 2 (NRF2)ovarian canceroxidative stressp53reactive oxygen species (ROS)SLC7A11xCT

Identifiers

PMID38203758
PMCPMC10779187
OpenAlexW4390502562

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.