Evidence map›Paper›PMID 26327509›Full record

ArticleOncotarget2015

High casein kinase 1 epsilon levels are correlated with better prognosis in subsets of patients with breast cancer.

Jose Luis Lopez-Guerra, Eva M Verdugo-Sivianes, Daniel Otero-Albiol, Begoña Vieites, Maria J Ortiz-Gordillo, Jose M De León, Juan M Praena-Fernandez, Juan J Marin, Amancio Carnero

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

7 citing papers in PubMed, 9 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

9 authors at 4 institutions in 1 country.

Jose Luis Lopez-GuerraInstituto de Biomedicina de Sevilla (IBIS/HUVR/CSIC/Universidad de Sevilla), Seville, Spain.
Eva M Verdugo-SivianesInstituto de Biomedicina de Sevilla (IBIS/HUVR/CSIC/Universidad de Sevilla), Seville, Spain.
Daniel Otero-AlbiolInstituto de Biomedicina de Sevilla (IBIS/HUVR/CSIC/Universidad de Sevilla), Seville, Spain.
Begoña VieitesDepartment of Pathology, University Hospital Virgen Del Rocío, Seville, Spain.
Maria J Ortiz-GordilloDepartment of Radiation Oncology, University Hospital Virgen del Rocío, Seville, Spain.
Jose M De LeónUnidad Funcional de Patología Mamaria, University Hospital Virgen Del Rocío, Seville, Spain.
Juan M Praena-FernandezMethodology Unit- Fundación Pública Andaluza para la Gestión de la Investigación en Salud de Sevilla, Virgen del Rocío University Hospital, Seville, Spain.
Juan J MarinInstituto de Biomedicina de Sevilla (IBIS/HUVR/CSIC/Universidad de Sevilla), Seville, Spain.
Amancio CarneroInstituto de Biomedicina de Sevilla (IBIS/HUVR/CSIC/Universidad de Sevilla), Seville, Spain.
Hospital Universitario Virgen del Rocío · ESUniversidad de Sevilla · ESConsejo Superior de Investigaciones Científicas · ESInstituto de Biomedicina de Sevilla · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Reliable biological markers that predict breast cancer (BC) outcomes after multidisciplinary therapy have not been fully elucidated. We investigated the association between casein kinase 1 epsilon (CK1ε) and the risk of recurrence in patients with BC. Using 168 available tumor samples from patients with BC treated with surgery +/- chemo(radio)therapy, we scored the CK1ε expression as high (≥ 1.5) or low (<1.5) using an immunohistochemical method. Kaplan-Meier analysis was performed to assess the risk of relapse, and Cox proportional hazards analyses were utilized to evaluate the effect of CK1ε expression on this risk. The median age at diagnosis was 60 years (range 35-96). A total of 58% of the patients underwent breast conservation surgery, while 42% underwent mastectomy. Adjuvant chemotherapy and radiation therapy were administered in 101 (60%) and 137 cases (82%), respectively. Relapse was observed in 24 patients (14%). Multivariate analysis found high expression of CK1ε to be associated with a statistically significant higher disease-free survival (DFS) in BC patients with wild-type p53 (Hazard ratio [HR] = 0.33; 95% CI, 0.12-0.91; P = 0.018) or poor histological differentiation ([HR] = 0.34; 95% CI, 0.12-0.94; P = 0.039) or in those without adjuvant chemotherapy ([HR] = 0.11; 95% CI, 0.01-0.97; P = 0.006). Our data indicate that CK1ε expression is associated with DFS in BC patients with wild-type p53 or poor histological differentiation or in those without adjuvant chemotherapy and thus may serve as a predictor of recurrence in these subsets of patients.

Indexed as

AdultAgedAged, 80 and overBiomarkers, TumorBreast NeoplasmsCasein Kinase 1 epsilonCell DifferentiationCell Line, TumorChemotherapy, AdjuvantDisease-Free SurvivalDisease ProgressionFemaleHumansImmunohistochemistryKaplan-Meier EstimateMastectomyBiomarkers, TumorCasein Kinase 1 epsilonTP53 protein, humanTumor Suppressor Protein p53breast cancercasein kinase 1 epsilon (CK1ε)disease-free survivaloutcomerelapse

Identifiers

PMID26327509
PMCPMC4745804
OpenAlexW1822344916

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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.