Literature DB >> 22961600

Subdivision of molecularly-classified groups by new gene signatures in breast cancer patients.

Athanasios Armakolas1, George P Stathopoulos, Adrianos Nezos, Apostolos Theos, Martha Stathaki, Michael Koutsilieris.   

Abstract

Gene expression patterns as well as gene interactions are under investigation for their involvement in tumour heterogeneity. The molecular classification of breast cancer based on hormone receptor expression, grade and HER2 receptor levels, is indicative but not adequate enough to complete the prognostic data. The objectives of this study were to validate the prognostic value of 19 genes, solely, and as parts of classifiers (sets of genes), in breast cancer patients and to determine whether the expression of these genes and classifiers is correlated with breast cancer molecular classification. Gene expression was examined in the blood of 88 breast cancer patients and 50 healthy controls using multiplex quantitative real-time PCR. Patients with a second primary malignancy showed a statistically significant difference when compared with: i) patients with a single breast cancer, for an 8-gene classifier (p<0.02); and ii) healthy individuals (classifier FBX033, FLJ339115) (p<0.01), with respect to gene expression. The classifier ENY2, USP38 was associated with the development of primary breast cancer. A newly established classifier (ENY2, USP38, RPS7, Osbpl-1 and ETF1) indicated a statistically significant association with HER2 subtype patients, compared to patients with a different molecular classification (p<0.04). The gene FLJ33915 was differentially expressed in a subgroup of HER2-positive patients with infiltrated axillary lymph nodes (p<0.028). We validated the prognostic value of 4 classifiers for primary and second primary malignancy. Evidence of a classifier predicting the HER2 subtype and the gene FLJ33915 which subdivides HER2 subtype patients is also presented.

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Year:  2012        PMID: 22961600     DOI: 10.3892/or.2012.2018

Source DB:  PubMed          Journal:  Oncol Rep        ISSN: 1021-335X            Impact factor:   3.906


  4 in total

1.  Cytoplasmic ATXN7L3B Interferes with Nuclear Functions of the SAGA Deubiquitinase Module.

Authors:  Wenqian Li; Boyko S Atanassov; Xianjiang Lan; Ryan D Mohan; Selene K Swanson; Aimee T Farria; Laurence Florens; Michael P Washburn; Jerry L Workman; Sharon Y R Dent
Journal:  Mol Cell Biol       Date:  2016-10-28       Impact factor: 4.272

2.  The deubiquitinase USP38 affects cellular functions through interacting with LSD1.

Authors:  Wenbin Liu; Qi Zhang; Yuanyuan Fang; Yanan Wang
Journal:  Biol Res       Date:  2018-11-29       Impact factor: 5.612

3.  Differential Second Primary Malignancy Occurrence After Breast Cancer According to HER2 Status: A Population-Based Study.

Authors:  Xiaoyi Lin; Xin Lin; Yingzi Li; Yuchen Zhang; Jiali Lin; Guochun Zhang
Journal:  Int J Gen Med       Date:  2021-11-24

4.  Computational analysis and verification of molecular genetic targets for glioblastoma.

Authors:  Liang Xue; Haibing Liu; Yehuang Chen; Liangfeng Wei; Jingfang Hong
Journal:  Biosci Rep       Date:  2020-06-26       Impact factor: 3.840

  4 in total

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