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UCL Division of Biosciences

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CDB Seminar - Prof Laura M Machesky

06 June 2024, 12:00 pm–1:00 pm

Photo of Prof Laura Machesky

Title: Mechanosensing in the cancer microenvironment

This event is free.

Event Information

Open to

All

Availability

Yes

Cost

Free

Organiser

Michael Wright – Cell and Developmental Biology

Abstract: Pancreatic cancer is highly metastatic, with a 5-year survival rate of less than 10%. Tumours are hallmarked by accumulation of highly fibrotic extracellular matrix, which correlates with poor prognosis and spread to organs such as liver, lung and peritoneal cavity. Our aim is to understand the molecular connections between force sensing and aggressiveness of tumour cells. We recently discovered a connection between mechanosensing, invasive migration and metabolic supply/demand in pancreatic cancer cells. I will discuss our model for how cells align their cytoskeletal polarity with their metabolic machinery to meet the high demands of the cancer microenvironment. If we can better model and understand this alignment, we can hope to find new ways to target the aggressiveness and spread of pancreatic cancer.

Suggested references:

  • Papalazarou V, Zhang T, Paul NR, Juin A, Cantini M, Maddocks ODK, Salmeron-Sanchez M, Machesky LM. The creatine-phosphagen system is mechanoresponsive in pancreatic adenocarcinoma and fuels invasion and metastasis. Nat Metab. 2020 Jan;2(1):62-80. doi: 10.1038/s42255-019-0159-z. Epub 2020 Jan 20. PMID: 32694686
  • Papalazarou V, Drew J, Juin A, Spence HJ, Whitelaw J, Nixon C, Salmeron-Sanchez M, Machesky LM. Collagen VI expression is negatively mechanosensitive in pancreatic cancer cells and supports the metastatic niche. J Cell Sci. 2022 Dec 15;135(24):jcs259978. doi: 10.1242/jcs.259978. Epub 2022 Dec 22. PMID: 36546396; PMCID: PMC9845737

Zoom: https://ucl.zoom.us/j/98418261199

Host: Barbara Conradt and Sandip Patel

About the Speaker

Prof Laura M Machesky

Sir William Dunn Professor of Biochemistry at University of Cambridge

Cell migration allows the shaping of complex tissues during development, the homing of immune cells and also the escape of cancer cells from a tumour during metastasis.  During their journeys, cells encounter environments of varying stiffness, texture and composition.  They respond to environmental forces with changes in shape, adhesion and signaling.  Tumours create stressful environments, imposing challenges of starvation, pressure and physical barriers on cells that require plastic adaptive behaviour.  Tumours frequently are stiffer than normal tissues due to fibrotic extracellular matrix and compression forces due to their rapid growth.  Cancer metastasis remains the most deadly aspect of solid tumours and the most intractable. We are interested in how the extracellular environment shapes the responses of cells and drives activities such as migration, extracellular matrix remodeling and energy flux.  We recently discovered that pancreatic cancer cells can sense the stiffness of their environment and respond not only with changes in migration, but also with metabolic adaptations that fuel enhanced invasiveness.  This led us to hypothesise that cells couple their metabolic machinery to their cytoskeletons to optimise energy flow during stressful energy-consuming activities, such as invasion of extracellular matrix.  Cells can also repurpose their actin cytoskeletons to take up nutrients via macropinocytosis and phagocytosis and thus address energy shortages.  We study how cells make decisions about whether to use their cytoskeleton to eat or to walk and thus how they achieve plasticity to survive various environmental challenges.

More about Prof Laura M Machesky