Breast Neoplasms Clinical Trial
Official title:
Study of Metabolites Markers in Adjuvant Breast Cancer
The breast cancer is composed of multiple biological entities. Recent progress in molecular
biology, DNA or RNA chip, permitted the global tumour genome or transcriptome study. Those
technics, leads to an increased in the molecular biology knowledge and a better oncogenesis
understanding. Breast cancer taxonomy was established following the tumor genetic profile.
Moreover this classification is incomplete and didn't include the metabolic pathways other
than hormonal or HER2 pathways.
The metabolomics is an expanding field of research exploring the metabolites in cells,
tissues or biologics fluids. It allows assessing the variation activation of the different
cellular metabolic pathways. In oncology, it could highlight the main metabolic disturbances,
the interaction of tumor cells and to identify the metabolic pathways involved in oncogenesis
using the tumor cells metabolites profiles.
Compared to genomic, the metabolomics integrated the impact of the cells environments on the
cells biology. The cells environment plays, in fact, a key role in the oncogenesis and in the
tumor cells phenotypes. The metabolomics, thus being a complementary approach of the genomic
in order to assess a better knowledge of the impact of the extracellular environment on the
tumor cell phenotype. In addition, the metabolomics analyses are fast and not expensive
compatible with routine practice.
The main objective of this study is to highlight a metabolic alteration specific to certain
tumors phenotypes in order to have better understanding of the biology of the numerous breast
cancer entities and find some biomarkers which could be some possible therapeutic target.
Using a high resolution mass spectrometer, the investigators will analyze 52 tumor samples
from frozen breast surgical specimen preserved in the Centre Antoine lacassagne tumor bank.
The tissue analysis could be associated with a serum sample analysis from the frozen serum
bank of the Centre Antoine Lacassagne. With 30 patients who performed a 18 FDG-PET before the
surgery, The investigators will analyzed the correlation between the tumoral activation of
the glycolysis pathways, quantified with mass spectroscopy and the 18FDG uptake. Using the 17
frozen serums available, the investigators will perform a screening to identify some
metabolites or metabolites profile which could be detected in the serum in order to develop a
new liquid biopsy approach. This study is a retrospective study based on data and sample
already available in the center and collected during the routine practice.
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