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http://purl.uniprot.org/citations/28859055http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/28859055http://www.w3.org/2000/01/rdf-schema#comment"

Background

Cancer cell proliferation is a critical feature in classifying and predicting the outcome of breast carcinoma. Separase has a central role in cell cycle progression in unleashing sister-chromatids at anaphase onset. Abnormally functioning separase is known to lead to chromosomal instability.

Methods

The study comprises 349 breast carcinoma patients treated in Central Hospital of Central Finland. The prognostic value, role as a proliferation marker and regulatory interactions of separase are evaluated by immunohistochemical and double- and triple-immunofluorescence (IF) detections based on complete clinical data and >22-year follow-up of the patient material.

Results

In our material, abnormal separase expression predicted doubled risk of breast cancer death (P<0.001). Up to 11.3-year survival difference was observed when comparing patients with and without separase expressing cancer cell mitoses. Particularly, abnormal separase expression predicted impaired survival for luminal breast carcinoma (P<0.001, respectively). In multivariate analyses, abnormal separase expression showed independent prognostic value. The complex inhibitory interactions involving securin and cyclin B1 were investigated in double- and triple-IFs and revealed patient subgroups with aberrant regulation and expression patterns of separase.

Conclusions

In our experience, separase is a promising and clinically applicable proliferation marker. Separase expression shows strong and independent prognostic value and could be developed into a biomarker for treatment decisions in breast carcinoma, particularly defining prognostic subgroups among luminal carcinomas."xsd:string
http://purl.uniprot.org/citations/28859055http://purl.org/dc/terms/identifier"doi:10.1038/bjc.2017.301"xsd:string
http://purl.uniprot.org/citations/28859055http://purl.uniprot.org/core/author"Kuopio T."xsd:string
http://purl.uniprot.org/citations/28859055http://purl.uniprot.org/core/author"Nykanen M."xsd:string
http://purl.uniprot.org/citations/28859055http://purl.uniprot.org/core/author"Loyttyniemi E."xsd:string
http://purl.uniprot.org/citations/28859055http://purl.uniprot.org/core/author"Kronqvist P."xsd:string
http://purl.uniprot.org/citations/28859055http://purl.uniprot.org/core/author"Talvinen K."xsd:string
http://purl.uniprot.org/citations/28859055http://purl.uniprot.org/core/author"Gurvits N."xsd:string
http://purl.uniprot.org/citations/28859055http://purl.uniprot.org/core/date"2017"xsd:gYear
http://purl.uniprot.org/citations/28859055http://purl.uniprot.org/core/name"Br J Cancer"xsd:string
http://purl.uniprot.org/citations/28859055http://purl.uniprot.org/core/pages"1383-1391"xsd:string
http://purl.uniprot.org/citations/28859055http://purl.uniprot.org/core/title"Separase is a marker for prognosis and mitotic activity in breast cancer."xsd:string
http://purl.uniprot.org/citations/28859055http://purl.uniprot.org/core/volume"117"xsd:string
http://purl.uniprot.org/citations/28859055http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/28859055
http://purl.uniprot.org/citations/28859055http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/28859055
http://purl.uniprot.org/uniprot/#_B4DRU1-mappedCitation-28859055http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/28859055
http://purl.uniprot.org/uniprot/#_Q14674-mappedCitation-28859055http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/28859055
http://purl.uniprot.org/uniprot/Q14674http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/28859055
http://purl.uniprot.org/uniprot/B4DRU1http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/28859055