WANT A PROFILE LIKE THIS?
Create my FREE Plan Or learn about other options
John Cassidy
PeerJ Author
135 Points

Contributions by role

Author 100
Preprint Author 35

Contributions by subject area

Bioinformatics
Cell Biology
Genomics
Drugs and Devices
Orthopedics

John W Cassidy

PeerJ Author

Summary

Large-scale genomics projects such as The Cancer Genome Atlas and METABRIC have begun to unravel the diverse heterogeneity of human malignancies. Further to this intertumour heterogeneity, recent studies have highlighted the heterogeneity within a single tumour (intratumour heterogeneity). Although it is beginning to become apparent that clonal populations within a tumour can have clinically relevant effects, we are far from understanding the drivers of clonal dynamics.

Patient-derived tumour xenografts (PDXs) have emerged as a powerful technology capable of retaining the molecular heterogeneity of their originating sample. Our research aims to fully describe the clonal dynamics in a panel of breast cancer PDX models, how these vary between models and how clonal dynamics are affected by passage. Furthermore, we will investigate the clonal dynamics involved in the development of drug resistance and strategies to perturb these dynamics with novel therapeutics.

Cell Biology Genomics

Past or current institution affiliations

University of Cambridge
University of Glasgow

Websites

  • Google Scholar
  • Cambridge Cancer Centre

PeerJ Contributions

  • Articles 1
  • Preprints 1
April 19, 2016
BMP2/BMPR1A is linked to tumour progression in dedifferentiated liposarcomas
Hannah L. O’Neill, Amy P. Cassidy, Olivia B. Harris, John W. Cassidy
https://doi.org/10.7717/peerj.1957 PubMed 27114889
February 6, 2016 - Version: 1
BMPR1A signalling is linked to tumour progression in dedifferentiated liposarcomas: lessons for rhBMP2 use in spinal surgery
Hannah L O'Neill, Amy P Cassidy, Olivia B Harris, John W Cassidy
https://doi.org/10.7287/peerj.preprints.1719v1