Cruk Ci Phd Studentship: Dissecting Malignant Cell-intrinsic and

1 week ago


Cambridge, United Kingdom University of Cambridge Full time

**PhD studentship**: Dissecting malignant cell-intrinsic and -extrinsic drivers of pancreatic cancer metastasis

**Supervisor**: Dr Giulia Biffi

**Department/location**: Cancer Research UK Cambridge Institute

**Project details**

Cancer-associated fibroblasts (CAFs) have been shown to promote pancreatic cancer progression. Our laboratory and others have demonstrated that CAFs are characterised by different populations that can differentially contribute to tumour growth, metastasis formation, therapy response and immunosuppression.

This research project will investigate the interplay between different CAF populations and malignant cells in pancreatic primary tumours and metastases with the goal to design combinatorial therapeutic approaches.
The project will involve the use of genetically complex organoid-derived transplantation mouse models of pancreatic cancer, novel genetically engineered mouse models for the depletion of different CAF populations, in vitro three-dimensional pancreatic tumour organoid/fibroblast co-culture models, CRISPR-based technologies, bulk and single-cell RNA-sequencing, flow cytometry, multiplex immunofluorescence, and standard molecular biology and biochemistry techniques. A computational component may also be available, depending on the skills and preference of the student but most of the project will be wet-lab-based.

References/further reading 1) Lloyd E.G., Jihad M., Manansala J.S., Li W., Cheng P.S.W., Mucciolo G., Zaccaria M., Pinto Teles S., Araos Henríquez J., Harish S., Brais R., Ashworth S., Luo W., Johnson P.M., Veghini L., Vallespinos M., Corbo V., Biffi G. SMAD4 and KRAS status shape malignant-stromal crosstalk in pancreatic cancer. Cancer Res (2025).

2) Mucciolo G., Araos Henríquez J., Jihad M., Pinto Teles S., Manansala J.S., Li W., Ashworth S., Lloyd E.G., Cheng P.S.W., Luo W., Anand A., Sawle A., Piskorz A., Biffi G. ¬EGFR-activated myofibroblasts promote metastasis of pancreatic cancer. Cancer Cell (2024).

3) Cheng P.S.W., Zaccaria M., Biffi G. Functional heterogeneity of fibroblasts in primary tumors and metastases. Trends in Cancer (2024).

4) Biffi G. and Tuveson DA. Diversity and Biology of Cancer-associated Fibroblasts. Physiol Rev (2021). 5) Biffi G, et al. IL1-Induced JAK/STAT Signaling Is Antagonized by TGFbeta to Shape CAF Heterogeneity in Pancreatic Ductal Adenocarcinoma. Cancer Discov (2019). Preferred skills/knowledge Applicants are expected to have laboratory experience in tissue culture and molecular biology techniques (e.g. RNA/protein analyses). Experience in mouse work, organoids, CRISPR, flow cytometry and computational skills is highly desirable. Please note that working with laboratory mice throughout the PhD is an essential requirement.

**Funding** This four-year studentship includes full funding for University fees and an index-linked stipend starting at £22,500 for four years.

Applicants with relevant research experience, gained through Master's study or while working in a laboratory, are strongly encouraged to apply.

**How to apply**

The University has a responsibility to ensure that all employees are eligible to live and work in the UK.

**Key information**:
**Department/location**:
Cancer Research UK Cambridge Institute

**Salary**:
**Reference**:
SW47202

**Category**:
Studentships

**Date published**:
8 September 2025

**Closing date**:
17 October 2025



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