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Innovate photonic devices for digital histopathology

Ongoing

We will deliver cost-effective, compact, and quantitative imaging applications to disrupt medical diagnosis permitting bed-side digital histopathology.

In biomedical research, the limitations of current light sources hinder progress in crucial areas. Conventional instruments confine two-photon microscopy and time-resolved detection to specialised labs, impeding cancer research and diagnostics breakthroughs. With this in mind, the EU-funded HILIGHT project aims to overcome existing limitations and pave the way for transformative advancements in biomedical and healthcare applications. Specifically, it will introduce a miniaturised optical pulse burst source and cutting-edge sensing technology. Two key applications underscore its potential impact: instantaneous digital histopathology and cancer research. With a consortium comprising leading partners from five European countries, the collaborative effort is expected to facilitate faster diagnoses and more effective treatments.

The project objectives are to:

  1. innovate fabrication of ultra-fast near-infrared lasers to manufacture compact and cost-effective light sources for two-photon microscopy
  2. innovate fabrication of ultra-fast time-resolved detectors to implement flexible and quantitative detection schemes for histopathology and biomedical applications
  3. translate these technology innovation to healthcare and biomedical research with the direct involvement of commercial and academic partners.
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Meet the Principal Investigator(s) for the project

Dr Alessandro Esposito
Dr Alessandro Esposito - I joined the University of Brunel in 2022 as a Lecturer in Biosciences (epigenetics). I am looking forward to sharing with students my passion for understanding how cells and tissues work, particularly how cells make decisions and differ from each other despite sharing an identical genome. My journey started in Sanremo, a small town on the Riviera dei Fiori in Italy. Passionate about science, physics and biology, I moved to the Ligurian capital to complete my studies, where I obtained my BSc in Physics at the University of Genoa. I specialized in Biophysics, microscopy, and neurosciences. I then completed my PhD in Biophysics at the University of Utrecht (NL), while working at the European Neuroscience Institute in Goettingen (DL). I had the opportunity to develop microscopes dedicated to biochemical imaging and the study of molecular mechanisms underpinning neurodegenerative diseases. Meanwhile, I trained in cell and molecular biology aiming to work at the interface between disciplines. In 2007, I started a long stint of work at the University of Cambridge. First, I developed novel analytical tools contributing to redefining models of red blood cell homeostasis infected by P. falciparum (malaria). In recognition of my early work, I was awarded a Life Science Interface fellowship by the EPSRC in 2009 to develop heavily multiplexed biochemical imaging tools and applications. Soon after, I moved to the MRC Cancer Unit where I led the ‘Systems Microscopy initiative’ and retrained in cancer biology. My work developed along two research streams: i) the study of cellular responses to DNA damage and mutations in signalling pathways and ii) the innovation of biochemical imaging technologies. Within the Director group, my team contributed to revealing the vast cell-to-cell variability in stress responses of genetically identical cells, a feature of biological systems that hinder the efficacy of disease management and therapeutic efficacy. Since 2019, my primary focus has been to understand how DNA damage and mutations in KRAS derange homeostatic programmes leading to cancer, in particular in models of pancreatic and colorectal cancers.  My group combines multi-omics data with single-cell biochemical imaging techniques aiming to achieve a deeper understanding of cancer phenotypes during the earliest stages of carcinogenesis, with particular attention to cell-to-cell variability of non-genetic origin and cell-to-cell communication. After the closure of the MRC Cancer Unit in 2022, I started my new adventure at the University of Brunel. The majority of my work is dedicated to the study of non-genetic factors causing cell-to-cell variability in signalling and metabolic pathways. At the Centre of Genome Engineering and Maintainance, I aim to dissect epigenetic mechanisms underpinning cellular variability in fate decisions. 

Related Research Group(s)

dna

Genome Engineering and Maintenance - Diverse research network focused on molecular, cellular, organismal and computational aspects of genome biology.


Partnering with confidence

Organisations interested in our research can partner with us with confidence backed by an external and independent benchmark: The Knowledge Exchange Framework. Read more.


Project last modified 22/02/2024