Evidence map›Paper›PMID 18236071›Full record

ArticleVirchows Archiv : an international journal of pathology2008

Molecular characterisation of breast cancer patients at high and low recurrence risk.

Serena Bonin, Davide Brunetti, Elena Benedetti, Isabella Dotti, Nader Gorji, Giorgio Stanta

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Article in Virchows Archiv : an international journal of pathology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

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3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Serena BoninDepartment of Clinical, Morphological and Technological Sciences, International Centre for Genetic Engineering and Biotechnology, University of Trieste, Trieste, Italy.
Davide Brunetti
Elena Benedetti
Isabella Dotti
Nader Gorji
Giorgio Stanta

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The ability to predict the recurrence risk in breast cancer patients is not available for the individual. It is commonly accepted that the different clinical course of tumours with identical histology and stage are the result of differences at the molecular level. This case study of 80 patients affected by breast cancer looked at the messenger ribonucleic acid expression level of 22 genes, by using quantitative reverse transcriptase-polymerase chain reaction. Our results showed that a panel of seven genes is associated to patients' survival. Moreover, the combination of two couples of genes is able to define short- and long-living cohorts of patients. In particular, our findings strongly demonstrate that retinoblastoma (RB) and cyclin-dependent kinase 2 (CDK2) on one side and cytokeratin 8 (CK8) and epidermal growth factor receptor 2 (HER2) on the other may affect the clinical course of the disease in 56% of patients. Groups characterised by low RB and high CDK2 as with low CK8 and high HER2 have a higher risk of recurrences and death in 5 years. The identification of these sub-groups of patients with higher risk of early relapse could have further involvement in the selection of the cases to submit to therapy against HER2 or CDK2 as a possible therapy target.

Indexed as

Neoplasm Recurrence, LocalAgedBreast NeoplasmsCohort StudiesCyclin-Dependent Kinase 2Erb-b2 Receptor Tyrosine KinasesFemaleGene Expression Regulation, NeoplasticGenetic Predisposition to DiseaseHumansKeratin-8Middle AgedPhosphatidylinositol 3-KinasesProportional Hazards ModelsProto-Oncogene Proteins c-aktProto-Oncogene Proteins c-rafAKT3 protein, humanCDK2 protein, humanCyclin-Dependent Kinase 2Erb-b2 Receptor Tyrosine KinasesKeratin-8Phosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktProto-Oncogene Proteins c-rafRetinoblastoma Protein

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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.