Evidence map›Paper›PMID 34085098›Full record

ArticleJournal of cancer research and clinical oncology2021

Cytoplasmic LXR expression is an independent marker of poor prognosis for patients with early stage primary breast cancer.

Wanting Shao, Christina Kuhn, Doris Mayr, Nina Ditsch, Magdalena Kailuwait, Verena Wolf, Nadia Harbeck, Sven Mahner, Udo Jeschke, Vincent Cavaillès and 1 more

Erratum issuedOpen access · hybridAbstract read
In one paragraph

Article in Journal of cancer research and clinical oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

6 citing papers in PubMed, 11 citations in OpenAlex.

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  2. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 6 institutions in 4 countries.

Wanting ShaoDepartment of Obstetrics and Gynecology, Breast Center, LMU University Hospital, Munich, Germany.
Christina KuhnDepartment of Gynecology and Obstetrics, University Hospital Augsburg, Stenglinstr. 2, 86156, Augsburg, Germany.
Doris MayrDepartment of Pathology, LMU Munich, Munich, Germany.
Nina DitschDepartment of Gynecology and Obstetrics, University Hospital Augsburg, Stenglinstr. 2, 86156, Augsburg, Germany.
Magdalena KailuwaitDepartment of Obstetrics and Gynecology, Breast Center, LMU University Hospital, Munich, Germany.
Verena WolfDepartment of Obstetrics and Gynecology, Breast Center, LMU University Hospital, Munich, Germany.
Nadia HarbeckDepartment of Obstetrics and Gynecology, Breast Center, LMU University Hospital, Munich, Germany.
Sven MahnerDepartment of Obstetrics and Gynecology, Breast Center, LMU University Hospital, Munich, Germany.
Udo JeschkeDepartment of Obstetrics and Gynecology, Breast Center, LMU University Hospital, Munich, Germany. udo.jeschke@med.uni-muenchen.de.ORCID http://orcid.org/0000-0003-2623-3235
Vincent CavaillèsIRCM-Institut de Recherche en Cancérologie de Montpellier, INSERM U1194, Université Montpellier, Parc Euromédecine, 208 rue des Apothicaires, F-34298, Montpellier, France.
Sophie SixouDepartment of Obstetrics and Gynecology, Breast Center, LMU University Hospital, Munich, Germany.
Ludwig-Maximilians-Universität München · DEUniversity Hospital Augsburg · DECentre National de la Recherche Scientifique · FRFirst Affiliated Hospital Zhejiang University · CNInserm · FRLMU Klinikum · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe aim of this study was to investigate the expression of liver X receptors α/β (LXR) in primary breast cancer (BC) tissues and to analyze its correlations with clinicopathological parameters including patient survival.

methodsIn a well-characterized cohort of 305 primary BC, subcellular distribution of LXR was evaluated by immunohistochemistry. Correlations with clinicopathological characteristics as well as with patient outcome were analyzed.

resultsLXR was frequently localized in both nuclei and cytoplasms of BC cells, with stronger staining in nuclei. Total and nuclear LXR expression was positively correlated with ER and PR status. Overall survival analysis demonstrated that cytoplasmic LXR was significantly correlated with poor survival and appeared as an independent marker of poor prognosis, in stage I but not in stage II-III tumors

conclusionAltogether, these data suggest that cytoplasmic LXR could be defined as a prognostic marker in early stage primary BC.

Indexed as

Biomarkers, TumorBreast NeoplasmsCarcinoma, Ductal, BreastCarcinoma, LobularCytoplasmFemaleFollow-Up StudiesHumansLiver X ReceptorsMiddle AgedNeoplasm InvasivenessPrognosisRetrospective StudiesSurvival RateBiomarkers, TumorLiver X ReceptorsBreast cancerEarly stageLXRPrognostic markerSubcellular location

Identifiers

PMID34085098
PMCPMC8310839
OpenAlexW3165466146

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.