Evidence map›Paper›PMID 37770957›Full record

ArticleJournal of experimental & clinical cancer research : CR2023

Cystine/glutamate antiporter xCT deficiency reduces metastasis without impairing immune system function in breast cancer mouse models.

Roberto Ruiu, Chiara Cossu, Antonella Iacoviello, Laura Conti, Elisabetta Bolli, Luca Ponzone, Jolanda Magri, Alekya Rumandla, Enzo Calautti, Federica Cavallo

Abstract read
In one paragraph

Article in Journal of experimental & clinical cancer research : CR, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
–field-weighted citation impact
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

17 citing papers in PubMed.

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  13. Selective metabolic regulations by p53 mutant variants in pancreatic cancer.Journal of experimental & clinical cancer research : CR · 2024
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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

10 authors.

Roberto RuiuDepartment of Molecular Biotechnology and Health Sciences, Laboratory of Oncoimmunology, Molecular Biotechnology Center "Guido Tarone", University of Turin, Via Nizza 52, Turin, 10126, Italy.ORCID http://orcid.org/0000-0002-0431-2656
Chiara CossuDepartment of Molecular Biotechnology and Health Sciences, Laboratory of Oncoimmunology, Molecular Biotechnology Center "Guido Tarone", University of Turin, Via Nizza 52, Turin, 10126, Italy.
Antonella IacovielloDepartment of Molecular Biotechnology and Health Sciences, Laboratory of Oncoimmunology, Molecular Biotechnology Center "Guido Tarone", University of Turin, Via Nizza 52, Turin, 10126, Italy.
Laura ContiDepartment of Molecular Biotechnology and Health Sciences, Laboratory of Oncoimmunology, Molecular Biotechnology Center "Guido Tarone", University of Turin, Via Nizza 52, Turin, 10126, Italy.
Elisabetta BolliDepartment of Molecular Biotechnology and Health Sciences, Laboratory of Oncoimmunology, Molecular Biotechnology Center "Guido Tarone", University of Turin, Via Nizza 52, Turin, 10126, Italy.
Luca PonzoneDepartment of Molecular Biotechnology and Health Sciences, Laboratory of Epithelial Stem Cell Biology and Signaling, Molecular Biotechnology Center "Guido Tarone", University of Turin, Via Nizza 52, Turin, 10126, Italy.
Jolanda MagriDepartment of Molecular Biotechnology and Health Sciences, Laboratory of Oncoimmunology, Molecular Biotechnology Center "Guido Tarone", University of Turin, Via Nizza 52, Turin, 10126, Italy.
Alekya RumandlaDepartment of Molecular Biotechnology and Health Sciences, Laboratory of Oncoimmunology, Molecular Biotechnology Center "Guido Tarone", University of Turin, Via Nizza 52, Turin, 10126, Italy.
Enzo CalauttiDepartment of Molecular Biotechnology and Health Sciences, Laboratory of Epithelial Stem Cell Biology and Signaling, Molecular Biotechnology Center "Guido Tarone", University of Turin, Via Nizza 52, Turin, 10126, Italy.
Federica CavalloDepartment of Molecular Biotechnology and Health Sciences, Laboratory of Oncoimmunology, Molecular Biotechnology Center "Guido Tarone", University of Turin, Via Nizza 52, Turin, 10126, Italy. federica.cavallo@unito.it.ORCID http://orcid.org/0000-0003-4571-1060

Funding

Fondazione AIRC per la ricerca sul cancro Fondazione AIRC per la ricerca sul cancroFondazione AIRC per la ricerca sul cancro IG 2018 - ID. 21468Fondazione Ricerca Molinette Fondazione Ricerca MolinetteFondazione Umberto Veronesi Fondazione Umberto VeronesiUniversità degli Studi di Torino Università degli Studi di Torino
6 · The paper itself

Abstract

backgroundThe upregulation of antioxidant mechanisms is a common occurrence in cancer cells, as they strive to maintain balanced redox state and prevent oxidative damage. This includes the upregulation of the cystine/glutamate antiporter xCT, which plays a crucial role in protecting cancer cells from oxidative stress. Consequently, targeting xCT has become an attractive strategy for cancer treatment. However, xCT is also expressed by several types of immune cells where it has a role in proliferation and effector functions. In light of these observations, a comprehensive understanding of the specific role of xCT in the initiation and progression of cancer, as well as its potential impact on the immune system within the tumor microenvironment and the anti-tumor response, require further investigation.

methodsWe generated xCT

resultsxCT depletion in BALB-neuT/xCT

conclusionsxCT is dispensable for proper immune system function, thus supporting the safety of xCT targeting in oncology. Nevertheless, xCT is involved in several processes required for the metastatic seeding of mammary cancer cells, thus broadening the scope of xCT-targeting approaches.

Indexed as

Amino Acid Transport System y+Breast NeoplasmsGlutamic AcidNeoplasmsAnimalsAntioxidantsCystineMiceMice, KnockoutMice, TransgenicOxidative StressAmino Acid Transport System y+AntioxidantsCystineGlutamic AcidSlc7a11 protein, mouseBreast cancerImmune systemMetastasisMetastatic nicheSLC7A11xCT

Identifiers

PMID37770957
PMCPMC10540318

What OpenQuestion holds

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Registered trials

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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.