In Austria, one in nine deaths among male cancer patients is due to prostate cancer. According to Statistics Austria, around 6,000 men are diagnosed with the disease every year. While some prostate cancers develop slowly and require minimal treatment, there are more aggressive forms that progress very quickly. In order to be able to treat prostate cancer more efficiently, it is necessary to understand the complex processes in the tumour at the molecular level.
Back in 2015, a research team led by experimental pathologist Lukas Kenner from MedUni Vienna's Department of Pathology and the Department of Laboratory Animal Pathology at Vetmeduni recognised, using a mouse model, that the protein STAT3 has a surprising tumour-suppressing role in prostate cancer. It was shown at that time that patients with low levels of STAT3 in cancer cells experience significantly worse disease progression than patients with high levels. A follow-up study showed that there was a higher metabolic rate in prostate cancer tissue as against healthy prostate tissue. This provides the tumour with extra energy to grow and metastasise.
The latest study by PhD student Robert Wiebringhaus from Lukas Kenner's team and molecular biologist Brigitte Hantusch builds on these findings. For the recent study, prostate cancer tissue was separated from healthy tissue using a laser microscope and the proteome, i.e. the totality of the proteins present, was then analysed using mass spectrometry (proteomics analysis). This facilitated the analysis of thousands of different peptides and proteins. There was found to be a higher concentration of proteins of the intracellular mitochondrial respiratory chain in the more aggressive cancer tissue. Mitochondria are organelles, i.e. structurally delimited cell areas with a specific biological function, and are also referred to as the "powerhouses of the cells". In a machinery consisting of enzyme complexes, the so-called respiratory chain or "oxidative phosphorylation" produces energy-rich degradation products via the breakdown of sugar and, in a final step, these generate the universal energy carrier adenosine triphosphate (ATP). This is an important regulator of cellular energy-producing processes. Those cells with a particularly high energy requirement, such as cancer cells, can cover this demand via oxidative phosphorylation.
Two proteins of interest from proteomics analysis – NDUFS1 and ATP5O – were studied in more depth in a collection of samples from patients with associated clinical data. Using immunohistochemical staining and data analysis, these two proteins were shown to be associated with a lower probability of survival in more aggressive forms of prostate cancerFurther analyses of the transcriptome, which comprises all genes that are transcribed in the cell at a certain point in time, also showed a rectified shift in the concentration of mRNA (messenger ribonucleic acid). This means that there is a direct correlation between the genetic transcripts and the proteins produced. The current study by Wiebringhaus et al. represents an important step in establishing a link between NDUFS, ATP5O and cancer aggressiveness. NDUFS1 and ATP5O could therefore serve as additional immunohistochemical markers for aggressive prostate tumours and, at the same time, as new targets for cancer treatment.
Proteomic Analysis Identifies NDUFS1 and ATP5O as Novel Markers for Survival Outcome in Prostate Cancer.
Robert Wiebringhaus, Matteo Pecoraro, Heidi A. Neubauer, Karolína Trachtová, Bettina Trimmel, Maritta Wieselberg, Jan Pencik, Gerda Egger, Christoph Krall, Richard Moriggl, Matthias Mann, Brigitte Hantusch and Lukas Kenner