Researchers at NUH are harnessing machine learning to map cancers,
offering a clearer view of how cells within tumours behave to design
and develop more effective treaments.
Issue 6 | September 2024
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What if, like a tourist effortlessly traversing unfamiliar terrain with the help of a reliable navigation app, we could map every cell within a tumour — enabling us to visualise and understand not just which cells are present, but also their precise locations and how they ‘talk’ to one another?
Researchers call this approach ‘spatial biology’. Dr Anand Jeyasekharan, Senior Consultant, Department of Haematology-Oncology, National University Cancer Institute, Singapore, is leveraging the technique to battle cancer, where advanced imaging equipment is used to analyse cancer with high molecular detail.
Spatial biology strips down biological systems to their key components, such as gene and protein expression, analysing them in three dimensions. It explores how cells and molecules are distributed within and interact across a tissue, what their environment indicates about their behaviour, and where they are located and why.
Consider embryonic development — a process in which humans and other organisms grow from a single cell. By deciphering how various cell types organise into complex tissue architectures, and subsequently, into a final form, scientists can decode the mechanisms through which embryos develop, uncovering insights into organ and tissue formation.
In the context of oncology, tumours are dynamic ecosystems composed of malignant and non-malignant cell types — cancer cells, stromal cells and immune cells — that evolve rapidly in response to various internal and external factors.
“Studying the body’s reaction to cancer cells is like observing a battlefield where two armies are programmed to annihilate each other,” says Dr Jeyasekharan. “Examining cells in their natural context and understanding cell-to-cell communication within tumours could help us detect tumours faster, deliver more accurate diagnoses and identify key targets for personalised anti-cancer drugs.”
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