Evidence map›Paper›PMID 30524888›Full record

ArticleOncoimmunology

Bovine herpesvirus 4-based vector delivering the full length xCT DNA efficiently protects mice from mammary cancer metastases by targeting cancer stem cells.

Gaetano Donofrio, Giulia Tebaldi, Stefania Lanzardo, Roberto Ruiu, Elisabetta Bolli, Andrea Ballatore, Valeria Rolih, Francesca Macchi, Laura Conti, Federica Cavallo

Open access · goldAbstract read
In one paragraph

Article in Oncoimmunology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

27 citing papers in PubMed, 47 citations in OpenAlex.

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  12. Targeting Breast Cancer Stem Cells.International journal of biological sciences · 2023
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  17. System XFrontiers in pharmacology · 2022
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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 at 2 institutions in 1 country.

Gaetano DonofrioDepartment of Medical Veterinary Science, Università degli Studi di Parma, Parma, Italy.ORCID 0000-0002-8984-0377
Giulia TebaldiDepartment of Medical Veterinary Science, Università degli Studi di Parma, Parma, Italy.
Stefania LanzardoDepartment of Molecular Biotechnology and Health Sciences, Molecular Biotechnology Center, Università degli Studi di Torino, Torino, Italy.
Roberto RuiuDepartment of Molecular Biotechnology and Health Sciences, Molecular Biotechnology Center, Università degli Studi di Torino, Torino, Italy.ORCID 0000-0002-0431-2656
Elisabetta BolliDepartment of Molecular Biotechnology and Health Sciences, Molecular Biotechnology Center, Università degli Studi di Torino, Torino, Italy.ORCID 0000-0002-1550-2391
Andrea BallatoreDepartment of Molecular Biotechnology and Health Sciences, Molecular Biotechnology Center, Università degli Studi di Torino, Torino, Italy.
Valeria RolihDepartment of Molecular Biotechnology and Health Sciences, Molecular Biotechnology Center, Università degli Studi di Torino, Torino, Italy.ORCID 0000-0003-3923-9476
Francesca MacchiDepartment of Medical Veterinary Science, Università degli Studi di Parma, Parma, Italy.
Laura ContiDepartment of Molecular Biotechnology and Health Sciences, Molecular Biotechnology Center, Università degli Studi di Torino, Torino, Italy.ORCID 0000-0003-1780-098X
Federica CavalloDepartment of Molecular Biotechnology and Health Sciences, Molecular Biotechnology Center, Università degli Studi di Torino, Torino, Italy.ORCID 0000-0003-4571-1060
University of Turin · ITUniversity of Parma · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite marked advancements in its treatment, breast cancer is still the second leading cause of cancer death in women, due to relapses and distal metastases. Breast cancer stem cells (CSCs), are a cellular reservoir for recurrence, metastatic evolution and disease progression, making the development of novel therapeutics that target CSCs, and thereby inhibit metastases, an urgent need. We have previously demonstrated that the cystine-glutamate antiporter xCT (SLC7A11), a protein that was shown to be overexpressed in mammary CSCs and that plays a key role in the maintenance of their redox balance, self-renewal and resistance to chemotherapy, is a potential target for mammary cancer immunotherapy. This paper reports on the development of an anti-xCT viral vaccine that is based on the bovine herpesvirus 4 (BoHV-4) vector, which we have previously showed to be a safe vaccine that can transduce cells

Indexed as

bovine herpesvirus 4-based vectorcancer stem cellimmunotherapyMammary cancerxCT

Identifiers

PMID30524888
PMCPMC6279326
OpenAlexW2890585509

What OpenQuestion holds

Textmetadata
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.