Evidence map›Paper›PMID 29075961›Full record

ArticleMolecular diagnosis & therapy2018

Checkpoint Kinase 1 Expression Predicts Poor Prognosis in Nigerian Breast Cancer Patients.

Henry Okuchukwu Ebili, Victoria O Iyawe, Kikelomo Rachel Adeleke, Babatunde Abayomi Salami, Adekunbiola Aina Banjo, Chris Nolan, Emad Rakha, Ian Ellis, Andrew Green, Ayodeji Olayinka Johnson Agboola

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Article in Molecular diagnosis & therapy, 2018. 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
2.7field-weighted citation impact, top 8% 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, 12 citations in OpenAlex.

  1. Article
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  4. Biomarkers for Breast Adenocarcinoma Using In Silico Approaches.Evidence-based complementary and alternative medicine : eCAM · 2022
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  5. Article
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  8. Comprehensive Analysis of Candidate Diagnostic and Prognostic Biomarkers Associated with Lung Adenocarcinoma.Medical science monitor : international medical journal of experimental and clinical research · 2020
    Article
  9. Article
  10. Article
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 2 countries.

Henry Okuchukwu EbiliDepartment of Morbid Anatomy and Histopathology, Olabisi Onabanjo University, Sagamu Campus, Hospital Road, Sagamu, Ogun State, Nigeria. ebili.henry@oouagoiwoye.edu.ng.
Victoria O IyaweDepartment of Morbid Anatomy and Histopathology, Olabisi Onabanjo University, Sagamu Campus, Hospital Road, Sagamu, Ogun State, Nigeria.
Kikelomo Rachel AdelekeDepartment of Morbid Anatomy and Histopathology, Olabisi Onabanjo University, Sagamu Campus, Hospital Road, Sagamu, Ogun State, Nigeria.
Babatunde Abayomi SalamiDepartment of Surgery, Olabisi Onabanjo University, Ago-Iwoye, Nigeria.
Adekunbiola Aina BanjoDepartment of Morbid Anatomy and Histopathology, Olabisi Onabanjo University, Sagamu Campus, Hospital Road, Sagamu, Ogun State, Nigeria.
Chris NolanDivision of Cancer and Stem Cells, School of Medicine, University of Nottingham, Nottingham, UK.
Emad RakhaDivision of Cancer and Stem Cells, School of Medicine, University of Nottingham, Nottingham, UK.
Ian EllisDivision of Cancer and Stem Cells, School of Medicine, University of Nottingham, Nottingham, UK.
Andrew GreenDivision of Cancer and Stem Cells, School of Medicine, University of Nottingham, Nottingham, UK.
Ayodeji Olayinka Johnson AgboolaDepartment of Morbid Anatomy and Histopathology, Olabisi Onabanjo University, Sagamu Campus, Hospital Road, Sagamu, Ogun State, Nigeria.
Olabisi Onabanjo University · NGUniversity of Nottingham · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCheckpoint kinase 1 (CHEK1), a DNA damage sensor and cell death pathway stimulator, is regarded as an oncogene in tumours, where its activities are considered essential for tumourigenesis and the survival of cancer cells treated with chemotherapy and radiotherapy. In breast cancer, CHEK1 expression has been associated with an aggressive tumour phenotype, the triple-negative breast cancer subtype, an aberrant response to tamoxifen, and poor prognosis. However, the relevance of CHEK1 expression has, hitherto, not been investigated in an indigenous African population. We therefore aimed to investigate the clinicopathological, biological, and prognostic significance of CHEK1 expression in a cohort of Nigerian breast cancer cases. MATERIAL AND

methodsTissue microarrays of 207 Nigerian breast cancer cases were tested for CHEK1 expression using immunohistochemistry. The clinicopathological, molecular, and prognostic characteristics of CHEK1-positive tumours were determined using the Chi-squared test and Kaplan-Meier and Cox regression analyses in SPSS Version 16.

resultsNuclear expression of CHEK1 was present in 61% of breast tumours and was associated with tumour size, triple-negative cancer, basal-like phenotype, the epithelial-mesenchymal transition, p53 over-expression, DNA homologous repair pathway dysfunction, and poor prognosis.

conclusionsThe rate expression of CHEK1 is high in Nigerian breast cancer cases and is associated with an aggressive phenotype and poor prognosis.

Indexed as

Up-RegulationBiomarkers, TumorBreast NeoplasmsCell NucleusCheckpoint Kinase 1FemaleGene Expression Regulation, NeoplasticHumansNigeriaPrognosisSurvival AnalysisTissue Array AnalysisTumor BurdenBiomarkers, TumorCheckpoint Kinase 1CHEK1 protein, human

Identifiers

PMID29075961
OpenAlexW2766101490

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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.