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  *EPSRC* Novel Synthetic Biology Approach to Monitor Transient Tumour-Immune Cell Interaction in vivo


   School of Biological Sciences

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  Dr E Cachat, Dr Binzhi Qian  No more applications being accepted  Competition Funded PhD Project (European/UK Students Only)

About the Project

This project aims at monitoring the dynamic interactions between tumour cells and macrophages in cancer metastasis models, by combining synthetic biology and intra-vital imaging approaches.

Metastasis, the spreading of tumour cells to secondary organs, accounts for over 90% of death from cancer and is the most pressing challenge for cancer research. Mounting clinical and preclinical evidences indicate that tumour/immune cells interactions have profound effects on cancer progression to metastasis (Kitamura et al., 2015). Previous studies have illustrated that tumour cells interaction with macrophages, a type of innate immune cells, is particularly critical for metastasis (Qian et al., 2011). The interaction is dynamic and complex, as there are different macrophage subsets with pro- or anti- tumour function differentially regulated by tissue microenvironment. Intra-vital imaging provides a powerful method to illustrate dynamic cell-cell interaction in relevant in vivo tissue environment. However, recording these transient interactions and interpreting their effect on disease progression has been challenging.

Synthetic biology allows the engineering of new functions into cells through sensor and actuator synthetic systems. Recently, synthetic chimeric receptors have been developed and engineered in cells, to respond to contact with specific ligands presented on neighbouring cells (Morsut et al., 2016). In this project, new synthetic receptor cell lines will be developed to detect tumour cell interactions with different subsets of macrophages that bear distinct cell surface markers. These cells will report contact through fluorescent protein expression and allow real-time monitoring of macrophage/tumour cells interaction both in vitro and in mice cancer models, shedding light on the pivotal role played by these intercellular contacts in cancer progression. This project will provide novel insights into the disease mechanism and highlight potential therapeutic strategies to effectively treat this lethal disease.

The supervisory team provides complimentary expertise in mammalian synthetic biology (EC) and tumour-macrophage interaction and in vivo metastasis models (BZQ), to ensure the success of this multi-disciplinary project based at the UK Centre for Mammalian Synthetic Biology (School of Biology, UoE) and the Cancer Research UK Edinburgh Centre (School of Clinical Sciences, UoE). Within this project, the student will receive extensive training in scientific research skills and analytical methods, but also acquire specific skills in molecular and synthetic biology, as well as skills in in vivo cancer models, including intra-vital microscopy and multi-parameter flow cytometry.

Further Information

Elise Cachat: http://www.ed.ac.uk/biology/people/profile/ecachat
Bin-Zhi Qian: http://www.ed.ac.uk/cancer-centre/research/qian-group




Funding Notes

This project is eligible for EPSRC funding and is open to UK nationals (or EU students who have been resident in the UK for 3+ years immediately prior to the programme start date)

Deadline for applications: 27 July 2018

References

- Kitamura T, Qian BZ and Pollard JW. Immune cell promotion of metastasis. Nature Review Immunology 2015. 2:73-86.
- Qian BZ, Li J, Zhang H, Kitamura T, Campion LR, Kaiser EA, Zhang J, Snyder LA and Pollard JW. CCL2 recruits inflammatory monocytes to facilitate breast tumour metastasis. Nature 2011. 475:222-25.
- Morsut L, Roybal KT, Xiong X, Gordley RM, Coyle SM, Thomson M and Lim WA. Engineering customized cell sensing and response behaviors using synthetic notch receptors. Cell 2016. 164:780-791.


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