Research groups
Colleges
Bobby White
BA
DPhil Student
Focus: the tumour microenvironment in cancer evolution
I am fascinated by how chemical and physical forces are translated into longer-term changes in cell behaviour. Such cellular regulation is integral to cancer biology, and disentangling the underlying mechanisms yields actionable targets for clinical oncology. This is why I study Cancer Science.
Cancer growth and metastasis require adequate metabolism to power the relevant biological processes. Indeed, the metabolic profile of a cancer correlates with its prognosis. Acidity and diffusion-limited oxygen availability are signatures of the solid tumour microenvironment, yet limit metabolism in most human cells. In the Swietach Group, we propose that subpopulations of cells within a cancer are resilient to these adverse microenvironmental conditions and thus exhibit a survival advantage. In turn, aggressive cancer cell behaviours, which require an adequate metabolic rate, are selected for during the somatic evolution of a tumour. I investigate this hypothesis by manipulating the interplay between acidity, oxygen and metabolism using in vitro and in vivo models of colorectal cancer. I aim to define factors that can curtail selection pressures for metabolically resilient and aggressive cancer behaviours, offering interventions to disrupt cancer growth in patients. My research is funded by a Cancer Research UK studentship.
I joined the University of Oxford in 2017 to study Medicine. In 2019, I intercalated a BA in Medical Sciences, achieving First Class Honours and the Andrew Hopley Memorial Prize for Excellence in Medicine. During my BA, I undertook my Final Honours School research with the Swietach Group, investigating acid-regulated signalling in cell growth. I am now further intercalating this DPhil with the Swietach Group into my Medical degree.
Recent publications
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Protocol for separating cancer cell subpopulations by metabolic activity using flow cytometry.
Journal article
Blaszczak W. et al, (2024), STAR Protoc, 5
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Phenotypic screen of sixty-eight colorectal cancer cell lines identifies CEACAM6 and CEACAM5 as markers of acid resistance.
Journal article
Michl J. et al, (2024), Proc Natl Acad Sci U S A, 121
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Dynamic IL-6R/STAT3 signaling leads to heterogeneity of metabolic phenotype in pancreatic ductal adenocarcinoma cells.
Journal article
Blaszczak W. et al, (2023), Cell Rep, 43
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What can we learn about acid-base transporters in cancer from studying somatic mutations in their genes?
Journal article
White B. and Swietach P., (2023), Pflugers Arch
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Acid-adapted cancer cells alkalinize their cytoplasm by degrading the acid-loading membrane transporter anion exchanger 2, SLC4A2.
Journal article
Michl J. et al, (2023), Cell Rep, 42