Evidence map›Paper›PMID 29285256›Full record

ArticleOncotarget2017

Investigation of RIP140 and LCoR as independent markers for poor prognosis in cervical cancer.

Aurelia Vattai, Vincent Cavailles, Sophie Sixou, Susanne Beyer, Christina Kuhn, Mina Peryanova, Helene Heidegger, Kerstin Hermelink, Doris Mayr, Sven Mahner and 3 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.8field-weighted citation impact, top 25% 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

10 citing papers in PubMed, 17 citations in OpenAlex.

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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

13 authors at 5 institutions in 2 countries.

Aurelia VattaiDepartment of Gynaecology and Obstetrics, Ludwig-Maximilians University of Munich, 80337 Munich, Germany.
Vincent CavaillesInstitut de Recherche en Cancérologie de Montpellier (IRCM), INSERM U1194, Université Montpellier, F-34298 Montpellier, France.
Sophie SixouUniversité Toulouse III - Paul Sabatier, F-31062 Toulouse, France.
Susanne BeyerDepartment of Gynaecology and Obstetrics, Ludwig-Maximilians University of Munich, 80337 Munich, Germany.
Christina KuhnDepartment of Gynaecology and Obstetrics, Ludwig-Maximilians University of Munich, 80337 Munich, Germany.
Mina PeryanovaDepartment of Gynaecology and Obstetrics, Ludwig-Maximilians University of Munich, 80337 Munich, Germany.
Helene HeideggerDepartment of Gynaecology and Obstetrics, Ludwig-Maximilians University of Munich, 80337 Munich, Germany.
Kerstin HermelinkDepartment of Gynaecology and Obstetrics, Ludwig-Maximilians University of Munich, 80337 Munich, Germany.
Doris MayrDepartment of Pathology, Ludwig-Maximilians University of Munich, 81337 Munich, Germany.
Sven MahnerDepartment of Gynaecology and Obstetrics, Ludwig-Maximilians University of Munich, 80337 Munich, Germany.
Christian DanneckerDepartment of Gynaecology and Obstetrics, Ludwig-Maximilians University of Munich, 80337 Munich, Germany.
Udo JeschkeDepartment of Gynaecology and Obstetrics, Ludwig-Maximilians University of Munich, 80337 Munich, Germany.
Bernd KostDepartment of Gynaecology and Obstetrics, Ludwig-Maximilians University of Munich, 80337 Munich, Germany.
Klinikum rechts der Isar · DELudwig-Maximilians-Universität München · DEInserm · FRUniversität Hamburg · DEUniversité Toulouse III - Paul Sabatier · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionRIP140 (Receptor Interacting Protein) is involved in the regulation of oncogenic signaling pathways and in the development of breast and colon cancers. The aim of the study was to analyze the expression of RIP140 and its partner LCoR in cervical cancers, to decipher their relationship with histone protein modifications and to identify a potential link with patient survival.

methodsImmunohistochemical analyses were carried out to quantify RIP140 and LCoR expression in formalin-fixed paraffin-embedded tissue sections cervical cancer samples. Correlations of RIP140 and LCoR expression with histopathological variables were determined by correlation analyses. Survival rates of patients expressing low or high levels of RIP140 and LCoR were compared by Kaplan-Meier curves.

resultsRIP140 overexpression was associated with a significantly shorter overall survival of cervical cancer patients. This effect was significant in the squamous cell carcinoma subtype but not in adenocarcinomas. RIP140 is no longer a significant negative prognosticator for cervical cancer when LCoR expression is low. DISCUSSION: RIP140 is an independent predictor of poor survival of patients with cervical cancer. Patients with tumors expressing low levels of both RIP140 and LCoR showed a better survival compared to patients expressing high levels of RIP140. Modulation of RIP140 and LCoR may represent a novel targeting strategy for cervical cancer prevention and therapy.

Indexed as

adenocarcinomacervical carcinomaLCoRRIP140/NRIP1squamous cell carcinoma

Identifiers

PMID29285256
PMCPMC5739643
OpenAlexW2766758882

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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.