Opportunity Overview
This project will address this challenge using interdisciplinary systems biology approaches including computational modelling, experimental wet-lab work in cell lines, and validation in primary patient material and murine models.
Our computational/in vitro preliminary data suggests that mutations can re-wire the NF-KB signalling pathway, creating crosstalk between pro-survival/developmental signalling and pro-inflammatory signalling. One impact of this signalling crosstalk may be that mutated cells respond incorrectly to their microenvironment, and produce a pro-inflammatory response to pro-survival/developmental signals, resulting in microenvironment remodelling.
The student will perform computational modelling that predicts how mutations might alter the way B-cells cells interpret their environment. This work will leverage vast data available from cancer studies that spans the scales from mutations to outcomes. These predictions will then be tested in cell lines by measuring NF-KB activity and the cytokines expressed in mutated and unmutated cells using a combination of transfection/CRISPR-cas9 experiments to introduce mutated genes/knock-out genes respectively. Exciting results from the lab will be carried forward to lymph node biopsy samples, and cell line-derived xenograft models where cell lines with/without cross-talk driving mutations will be introduced and immune infiltration will be assayed using spectral flow cytometry.
Computational modelling...
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Start FreeSolicitation Details
| Issuing agency | BBSRC |
|---|---|
| Country | United Kingdom |
| Category | Research Development |
| Published | September 30, 2024 |
| Procurement stage | Active solicitation |
| Response due | September 29, 2028 |
| Status | Open — accepting responses |
| Official source | View original notice |
| Last verified | August 09, 2026 |
Source: UK Research and Innovation (UKRI) — Open Government Licence v3.0.
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