Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.768053
Title: Heterotypic cell-cell interactions between KrasG12D cells and normal neighbours in early pancreatic cancer
Author: Hill, William
ISNI:       0000 0004 7652 3086
Awarding Body: Cardiff University
Current Institution: Cardiff University
Date of Award: 2018
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Abstract:
At the initial stages of tumourigenesis, transformation occurs in a single cell within a healthy epithelial sheet. Competitive interactions between normal and Ras-transformed cells can drive the elimination of mutant cells from tissues to protect from carcinogenesis. Moreover, we have previously demonstrated that normal cells detect and eliminate Ras-transformed cells via differential EphA2 signalling. KrasG12D expressing cells (KrasG12D cells) initiate and drive the earliest stages of pancreatic cancer yet it is unclear if normal pancreatic cells can eliminate oncogenic cells. Here we use low level, stochastic induction of KrasG12D mutations in the pancreas to model the interaction of normal and transformed epithelial cells. We show that Ras-transformed cells adopt a contractile morphology and are eliminated from healthy tissue when present at low numbers. When surrounded by normal cells, KrasG12D cells become segregated, increase in compactness and are often extruded. We find that E-cadherin-based cell-cell contacts are downregulated and internalised in mutant cells when surrounded by normal neighbours in an EphA2-dependent manner. Our evidence also suggests that normal cells suppress progression of Ras-transformed cells to an early disease state. Together, this study suggests that non-transformed pancreatic epithelial cells can eliminate KrasG12D cells from the tissue via EphA2 signalling. These data identify a novel putative tumour-suppressive mechanism in the adult pancreas that mutant cells must first overcome to drive tumourigenesis. Understanding the earliest stages of pancreatic carcinogenesis will provide insight into how risk factors promote disease and may elucidate how pancreatic cancer spreads around the body.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.768053  DOI: Not available
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