SELDI-TOF proteomic profiling of breast carcinomas identifies clinicopathologically relevant groups of patients similar to previously defined clusters from cDNA expression.

Expression profiling and biomarker(s) discovery aim to provide means for tumour diagnosis, classification, therapy response and prognosis. The identification of novel markers could potentially lead to the building of robust early detection strategies and personalized, effective breast cancer therapies that would improve patient outcome. Recent evidence supports the hypothesis that genomic expression profiling using microarray analysis is a reliable method for breast cancer classification and prognostication. However, genes clearly do not act by themselves, or indeed they do not have catalytic or signalling capabilities. Hence, genetic biomarker information alone cannot perfectly predict cancer and its response to treatment. Genes clearly exert their effect after transcription through translation into active proteins. Consequently, postgenomic projects correlating protein expression profiles with tumour classification have led to some established biomarkers. In this regard, these biomarkers associate with disease prediction and can be associated with treatment response. Recently, Brozokova and colleagues demonstrated that surface-enhanced laser desorption ionization time of flight mass spectrometry (SELDI-TOF MS) profiling of breast cancer tissue proteomes can potentially expand the biomarker repertoire and our knowledge of breast cancer behaviour.

New technologies for predicting or classifying cancer are constantly evolving. Reported in this issue, a study by Brozokova and coworkers [1] demonstrates that protein expression profiling may enhance our accuracy of detection and prognostication in breast cancer. It has become clear that histological analysis is not, by itself, adequate in predicting clinical outcome and insensitive in identifying the optimal therapeutic strategy in many cancers [2]. Individual tumours often carry a specific molecular footprint that may have more in common with another tumour of different histological type, and emphasis is now shifting toward specific clinical management of these individual molecular patterns rather than a blanket, 'one size fits all' therapy for tumours with common histology. Breast cancer is a major killer that remains challenging in terms of molecular complexity and treatment response. The multifactorial nature of breast cancer lends itself to the use of multiple biomarkers for early detection, monitoring of response to therapy, and clinical outcome prediction. Microarray-based gene expression profiling has provided new insight into the molecular intricacy of breast cancer and has provided a clinically valuable breast cancer classification system [3-5]. However, cDNA profiles do not provide a complete picture. After all, it is proteins in all their many post-translational coats -and not RNA transcripts – that run the intracellular machinery. Thus, there is a need to identify new, more accurate markers of disease. Enter proteomic profiling.

Brozokova and colleagues [1] employed proteomics using surface-enhanced laser desorption ionization time of flight mass spectrometry (SELDI-TOF MS) to identify relevant molecular signatures of breast cancer. This work revealed subgroups of patients with differential co-expression of protein peaks in diverse tumour subclasses, and demonstrated differing clinicopathological characteristics in tumour type, nuclear grade, hormonal status, mucin 1, and cyto-keratin 5/6 or 14 between these groups. Significantly, the patient subgroups identified by hierarchical clustering of SELDI-TOF MS peaks were analogous to breast cancer classifications based on gene expression profiling, classifying the tumours into luminal, basal and HER2 subtypes [3].

Use of SELDI TOF MS has three main advantages. First, the reliability of signatures of breast cancer gene expression is becoming increasingly acknowledged, and proteomic profiling is considered to be the final step in drawing a biological picture of cancers. Second, despite variable biomarker detection from separate studies [6-10], mass spectrometry represents an additional approach to mine novel proteins. Third, these new biomarkers may well relate to tumour development and behaviour extrapolated from minimal starting material and high throughput proteomic capabilities.

A fundamental part of the study conducted by Brozokova and colleagues was the progression from descriptive knowledge of protein peak signature classification to the identification of two proposed biomarkers. Here, they identified two significant biomarkers, namely heat shock protein (HSP)27 and annexin V, which were over-expressed in subcohorts of patients corresponding to luminal A subtypes. Significantly, HSP27 appears to be a bona fide biomarker, because it was shown to be elevated in oestrogen receptor positive patients in a previous study [11]. Further confirmation has been reported; specifically, HSP27 and a related protein isoform of the annexin family were found to correlate with chemo-resistance in breast cancer [12].

Evidently, SELDI-TOF MS and mass spectrometry in general allow a more rapid identification of many potential biomarkers from biological samples. This study and those described above support the use of SELDI as a complementary method of breast cancer classification and biomarker discovery. The identification of biomarker proteins in this work is a key element in elucidating the relevant pathways of breast cancer, and highlights the possibility that some of these biomarkers may be monitored/targeted in future treatment modalities. There are some issues regarding SELDI's role in disease prognosis and classification, which would benefit from larger, multicentre validation studies. However, as mass spectrometry technology evolves, it is becoming increasingly clear that changes in proteomic profiles of breast cancer will aid in disease stratification and prognostication, and will significantly help to guide selection of treatment regimens.

Abbreviations

HSP = heat shock protein; SELDI-TOF MS = surface-enhanced laser desorption ionization time of flight mass spectrometry.

Competing interests

The authors declare that they have no competing interests.