4.6 Article

The Breast Cancer Protein Co-Expression Landscape

Journal

CANCERS
Volume 14, Issue 12, Pages -

Publisher

MDPI
DOI: 10.3390/cancers14122957

Keywords

breast cancer; proteomics; co-expression networks; protein-protein interactions

Categories

Funding

  1. National Institute of Genomic Medicine, Mexico
  2. Laboratorio Nacional de Ciencias de la Complejidad, from the Universidad Nacional Autonoma de Mexico
  3. 2016 Marcos Moshinsky Fellowship in the Physical Sciences

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This study explores the abundance and co-occurrence patterns of proteins in breast cancer cells and healthy cells. The findings suggest that these differences in proteins may be associated with relevant aspects of tumor biology. The results provide valuable information for the development of diagnostic, prognostic, and therapeutic tools for cancer.
Simple Summary Proteins are among the most fundamental building blocks and molecular players behind the functions of cells and tissues. Their abundance and interaction patterns shape, to a large extent, what happens at the cellular and organ levels. This is also true regarding tumor tissues. In this work, we explored the patterns of abundance and co-occurrence of a large number of proteins in breast cancer cells and their healthy counterparts. We discovered the main differences and tried to see whether those differences may be associated with relevant aspects of the biology of these tumors. Our final goal is to provide information to empower cancer clinicians and pharmacologists to develop better diagnostic, prognostic, and therapeutic tools. Breast cancer is a complex phenotype (or better yet, several complex phenotypes) characterized by the interplay of a large number of cellular and biomolecular entities. Biological networks have been successfully used to capture some of the heterogeneity of intricate pathophenotypes, including cancer. Gene coexpression networks, in particular, have been used to study large-scale regulatory patterns. Ultimately, biological processes are carried out by proteins and their complexes. However, to date, most of the tumor profiling research has focused on the genomic and transcriptomic information. Here, we tried to expand this profiling through the analysis of open proteomic data via mutual information co-expression networks' analysis. We could observe that there are distinctive biological processes associated with communities of these networks and how some transcriptional co-expression phenomena are lost at the protein level. These kinds of data and network analyses are a broad resource to explore cellular behavior and cancer research.

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