Evidence map›Paper›PMID 36057630›Full record

ArticleCell death & disease2022

ROBO3s: a novel ROBO3 short isoform promoting breast cancer aggressiveness.

Marcel Werner, Anna Dyas, Iwan Parfentev, Geske E Schmidt, Iga K Mieczkowska, Lukas C Müller-Kirschbaum, Claudia Müller, Stefan Kalkhof, Oliver Reinhardt, Henning Urlaub and 4 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 52% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

14 authors at 6 institutions in 2 countries.

Marcel Werner *Department of General, Visceral and Pediatric Surgery, University Medical Center Göttingen, Göttingen, Germany.ORCID 0000-0002-6328-048X
Anna Dyas *Department of General, Visceral and Pediatric Surgery, University Medical Center Göttingen, Göttingen, Germany.
Iwan Parfentev *Bioanalytical Mass Spectrometry group, Max Planck Institute for Multidisciplinary Sciences, Göttingen, Germany.
Geske E SchmidtDepartment of Gastroenterology, Gastrointestinal Oncology and Endocrinology, University Medical Center Göttingen, Göttingen, Germany.
Iga K MieczkowskaDepartment of General, Visceral and Pediatric Surgery, University Medical Center Göttingen, Göttingen, Germany.ORCID 0000-0002-3684-3945
Lukas C Müller-KirschbaumDepartment of General, Visceral and Pediatric Surgery, University Medical Center Göttingen, Göttingen, Germany.ORCID 0000-0003-1885-6694
Claudia MüllerDepartment of Preclinical Development and Validation, Fraunhofer Institute for Cell Therapy and Immunology, Leipzig, Germany.
Stefan KalkhofDepartment of Preclinical Development and Validation, Fraunhofer Institute for Cell Therapy and Immunology, Leipzig, Germany.
Oliver ReinhardtTranslational Molecular Imaging, Max-Planck Institute for Multidisciplinary Sciences, Göttingen, Germany.
Henning UrlaubBioanalytical Mass Spectrometry group, Max Planck Institute for Multidisciplinary Sciences, Göttingen, Germany.
Frauke AlvesTranslational Molecular Imaging, Max-Planck Institute for Multidisciplinary Sciences, Göttingen, Germany.
Julia GallwasDepartment of Gynecology and Obstetrics, University Medical Center Göttingen, Göttingen, Germany.
Evangelos ProkakisDepartment of Gynecology and Obstetrics, University Medical Center Göttingen, Göttingen, Germany. eprokak@gwdg.de.ORCID 0000-0001-9297-1821
Florian WegwitzDepartment of Gynecology and Obstetrics, University Medical Center Göttingen, Göttingen, Germany. fwegwit@gwdg.de.ORCID 0000-0003-0750-6998
Universitätsmedizin Göttingen · DEMax Planck Institute for Multidisciplinary SciencesFraunhofer Institute for Cell Therapy and Immunology · DEGesellschaft für wissenschaftliche Datenverarbeitung mbH Göttingen · DEHelmholtz Zentrum München · DEHutchison/MRC Research Centre · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Basal-like breast cancer (BLBC) is a highly aggressive breast cancer subtype frequently associated with poor prognosis. Due to the scarcity of targeted treatment options, conventional cytotoxic chemotherapies frequently remain the standard of care. Unfortunately, their efficacy is limited as BLBC malignancies rapidly develop resistant phenotypes. Using transcriptomic and proteomic approaches in human and murine BLBC cells, we aimed to elucidate the molecular mechanisms underlying the acquisition of aggressive and chemotherapy-resistant phenotypes in these mammary tumors. Specifically, we identified and characterized a novel short isoform of Roundabout Guidance Receptor 3 (ROBO3s), upregulated in BLBC in response to chemotherapy and encoding for a protein variant lacking the transmembrane domain. We established an important role for the ROBO3s isoform, mediating cancer stem cell properties by stimulating the Hippo-YAP signaling pathway, and thus driving resistance of BLBC cells to cytotoxic drugs. By uncovering the conservation of ROBO3s expression across multiple cancer types, as well as its association with reduced BLBC-patient survival, we emphasize its potential as a prognostic marker and identify a novel attractive target for anti-cancer drug development.

Indexed as

Antineoplastic AgentsBreast NeoplasmsMammary Neoplasms, AnimalAnimalsFemaleHumansMiceProtein IsoformsProteomicsReceptors, Cell SurfaceRoundabout ProteinsAntineoplastic AgentsProtein IsoformsReceptors, Cell SurfaceROBO3 protein, humanRoundabout Proteins

Identifiers

PMID36057630
PMCPMC9440919
OpenAlexW4294415814

What OpenQuestion holds

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LicenceCC BY
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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.