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Increased macroH2A1.1 Expression Correlates with Poor Survival of Triple-Negative Breast Cancer Patients
- Source :
- PLoS ONE, PLoS ONE, Public Library of Science, 2014, 9 (6), pp.e98930. ⟨10.1371/journal.pone.0098930⟩, PLoS ONE, Vol 9, Iss 6, p e98930 (2014)
- Publication Year :
- 2014
- Publisher :
- HAL CCSD, 2014.
-
Abstract
- PurposeEpithelial-Mesenchymal Transition (EMT) features appear to be key events in development and progression of breast cancer. Epigenetic modifications contribute to the establishment and maintenance of cancer subclasses, as well as to the EMT process. Whether histone variants contribute to these transformations is not known. We investigated the relative expression levels of histone macroH2A1 splice variants and correlated it with breast cancer status/prognosis/types.MethodsTo detect differential expression of macroH2A1 variant mRNAs in breast cancer cells and tumor samples, we used the following databases: GEO, EMBL-EBI and publisher databases (may-august 2012). We extracted macroH2A1.1/macroH2A1 mRNA ratios and performed correlation studies on intrinsic molecular subclasses of breast cancer and on molecular characteristics of EMT. Associations between molecular and survival data were determined.ResultsWe found increased macroH2A1.1/macroH2A1 mRNA ratios to be associated with the claudin-low intrinsic subtype in breast cancer cell lines. At the molecular level this association translates into a positive correlation between macroH2A1 ratios and molecular characteristics of the EMT process. Moreover, untreated Triple Negative Breast Cancers presenting a high macroH2A1.1 mRNA ratio exhibit a poor outcome.ConclusionThese results provide first evidence that macroH2A1.1 could be exploited as an actor in the maintenance of a transient cellular state in EMT progress towards metastatic development of breast tumors.
- Subjects :
- Epigenomics
Microarrays
[SDV]Life Sciences [q-bio]
Cancer Treatment
Gene Expression
Triple Negative Breast Neoplasms
Epigenesis, Genetic
Histones
Molecular Cell Biology
Breast Tumors
Medicine and Health Sciences
MESH: Epigenesis, Genetic
Triple-negative breast cancer
ComputingMilieux_MISCELLANEOUS
MESH: Histones
Regulation of gene expression
Multidisciplinary
biology
Chromosome Biology
MESH: Alternative Splicing
Obstetrics and Gynecology
Histone Modification
Genomics
MESH: Gene Expression Regulation, Neoplastic
MESH: Triple Negative Breast Neoplasms
Prognosis
Chromatin
3. Good health
Gene Expression Regulation, Neoplastic
Bioassays and Physiological Analysis
Histone
Oncology
MESH: Survival Analysis
Medicine
Epigenetics
Genetic Engineering
Transcriptome Analysis
Research Article
Biotechnology
Epithelial-Mesenchymal Transition
MESH: Cell Line, Tumor
Science
Research and Analysis Methods
MESH: Prognosis
Epigenetic Therapy
Molecular Genetics
Breast cancer
Cell Line, Tumor
Breast Cancer
Genetics
Cancer Genetics
medicine
Humans
Epithelial–mesenchymal transition
MESH: Humans
Biology and Life Sciences
Computational Biology
Cancers and Neoplasms
Cancer
Cell Biology
Genome Analysis
medicine.disease
Survival Analysis
Alternative Splicing
MESH: Epithelial-Mesenchymal Transition
Genetics of Disease
biology.protein
Cancer research
Women's Health
Genome Expression Analysis
Subjects
Details
- Language :
- English
- ISSN :
- 19326203
- Database :
- OpenAIRE
- Journal :
- PLoS ONE, PLoS ONE, Public Library of Science, 2014, 9 (6), pp.e98930. ⟨10.1371/journal.pone.0098930⟩, PLoS ONE, Vol 9, Iss 6, p e98930 (2014)
- Accession number :
- edsair.doi.dedup.....55fcefd9fc34368d5d05822ceb401fea
- Full Text :
- https://doi.org/10.1371/journal.pone.0098930⟩