Abstract

Breast cancer is the most diagnosed cancer in women, accounting for approximately 40,000 deaths annually in the USA. In Tunisia, the incidence of breast cancer is approximately 19 new cases per 100,000 women per year. Significant advances have been made in the areas of detection and treatment, but a significant number of breast cancers are detected late. The enormous progress in proteomics, enabled by recent advances in MS (mass spectrometry), has brought protein analysis back into the limelight of breast cancer research, reviving old areas as well as opening new fields of study like early detection, prognosis, diagnosis, and therapy. Several proteomics technologies have been used to uncover molecular mechanisms associated with breast carcinoma at the global level to discover protein patterns that distinguish disease and disease-free states with high sensitivity and specificity. Breast cancer proteomics has already identified markers of potential clinical interest (such as the molecular chaperone alpha B-crystallin) and technological innovations such as large scale and high throughput analysis are now driving the field. In this review, we discuss the basic features of proteomic technologies, including MS, and we consider the main current applications and challenges of proteomics in breast cancer research, including (i) protein expression profiling of breast tumours, tumour cells, tumour fluids and the auto-immune response of the breast cancer cells. All of these applications continue to benefit from further technological advances, such as the development of proteomics methods, high-resolution, highsensitivity MS, SERPA approach, and advanced bioinformatics for data handling and interpretation.

Highlights

  • By comparing 2-DE profiles between tumor and non-tumor samples and using MALDI-TOF mass spectrometry of their trypsinized fragments, we report the identification of two proteins of interest, namely haptoglobin precursor and alpha-1- antitrypsin precursor, whose expression was altered in sera from infiltrating ductal breast carcinoma patients (Hamrita et al, 2009)

  • The data reported appears to confirm this for breast cancer patients as well, and suggest that molecular alterations leading to an immune reaction directed toward antigens related to the system of protein folding may be an important marker in breast carcinogenesis

  • The identification of reliable biomarkers to track breast cancer, which should provide a better classification of tumors, allow for personalized therapy and exciting challenge for the scientific and medical community

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Summary

Introduction

Proteomic analysis can be viewed as a genome-wide assay to differentiate distinct cellular states and to determine the molecular mechanisms that control them (Anderson et al, 1996). Biomarkers can be defined as cellular, biochemical, and molecular alterations by which normal, abnormal, or biologic processes can be recognized or monitored (Vercoutter-Edouart et al, 2001; Hondermarck, 2003). These alterations should be able to objectively measure and evaluate normal biological process, pathogenic processes (like breast cancer), to a therapeutic intervention.

Utility and recent advancements in the proteomics approaches
Sera samples
Cells and Tissue samples
Validation of the biomarkers
Findings
Conclusions
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