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Contact Details

Phone
+64 3 479 7797
Email
adele.woolley@otago.ac.nz
Position
Senior Lecturer
Department
Department of Pathology (Dunedin)
Qualifications
BPhEd BSc PGDipSci PhD(Otago)
Research summary
Cytoskeletal dynamics in cell cycle and cell migration
Teaching
  • PATH 201 Foundations of Human Diseases (course convenor)
  • PATH 302 Cancer Biology
  • MICN 301 Vertical Pathology Module
  • CMC 301 Cancer and Diabetes
Memberships
  • Australian and New Zealand Society for Cell and Developmental Biology
  • Federation of University Women
  • Dunedin Company of Physiologists
  • TEMTIA (Society of Epithelial-Mesenchymal transition)
  • Department of Pathology Teaching committee
  • BBiomedSc Operational Committee
Clinical
Cancer biology, and Inflammatory microenvironment in cancer and other inflammatory diseases

Research

One of our foci is on the cell cycle and cell migration, fundamental cellular processes that underpin many diseases, including cancer.

The cell cycle is the sequence of events by which cells faithfully replicate their DNA and then segregate the duplicated chromosomal DNA equally between two daughter cells. An intricate network of regulatory pathways ensures that each cell cycle event is performed correctly and in proper sequence. In healthy tissues, cell division is a well-controlled process during which both our duplicated genetic and cytoplasmic material is equally distributed over two newly formed daughter cells, such that after a round of cell division each daughter cell has a complete set of 46 chromosomes. Cancer arises as a consequence of uncontrolled cell division resulting in chromosomal instability.

We are also researching Metastasis (the movement of cancer cells to distant parts of the body). This is the primary cause of death in cancer patients. We are interested in understanding the regulation of cell cycle exit and early cell migration. We are also investigating the role of the microenvironment in both cancer and inflammatory diseases such as osteo- and rheumatoid arthritis.

We use experimental approaches to study changes in cellular processes that take place in disease. Ultimately, by understanding the dynamics of these cellular processes, we can provide a platform for intervention in disease. We aim to use these discoveries to develop biomarkers for specific disease states.

Additional details

The Woolley Laboratory

Publications

Wiles, A. K., Mehta, S., Millier, M., Woolley, A. G., Li, K., Parker, K., Kazantseva, M., Wilson, M., Young, K., Bowie, S., Ray, S., Slatter, T. L., Stamp, L. K., Hessian, P. A., & Braithwaite, A. W. (2023). Activated CD90/Thy-1 fibroblasts co-express the Δ133p53β isoform and are associated with highly inflamed rheumatoid arthritis. Arthritis Research & Therapy, 25, 62. doi: 10.1186/s13075-023-03040-8 Journal - Research Article

Shields, N. J., Peyroux, E. M., Campbell, K., Mehta, S., Woolley, A. G., Counoupas, C., Neumann, S., & Young, S. L. (2022). Calpains released from necrotic tumor cells enhance antigen cross-presentation to activate CD8+ T cells in vitro. Journal of Immunology, 209(9), 1635-1651. doi: 10.4049/jimmunol.2100500 Journal - Research Article

McDougall, L., Kueh, J. T. B., Ward, J., Tyndall, J. D. A., Woolley, A. G., Mehta, S., Stayner, C., Larsen, D. S., & Eccles, M. R. (2021). Chemical synthesis of the PAX protein inhibitor EG1 and its ability to slow the growth of human colorectal carcinoma cells. Frontiers in Oncology, 11, 709540. doi: 10.3389/fonc.2021.709540 Journal - Research Article

Mehta, S., Algie, M., Al-Jabry, T., McKinney, C., Kannan, S., Verma, C. S., … Parker, K., Henderson, L., Gould, M. L., Bhatia, P., Harfoot, R., … Kleffmann, T., … Woolley, A. G., … Braithwaite, A. (2020). Critical role for cold shock protein YB-1 in cytokinesis. Cancers, 12, 2473. doi: 10.3390/cancers12092473 Journal - Research Article

Mehta, S., McKinney, C., Algie, M., Verma, C. S., Kannan, S., Harfoot, R., … Gould, M. L., Parker, K., … Cunliffe, H. E., … Kleffmann, T., Braithwaite, A. W., & Woolley, A. G. (2020). Dephosphorylation of YB-1 is required for nuclear localisation during G2 phase of the cell cycle. Cancers, 12(2), 315. doi: 10.3390/cancers12020315 Journal - Research Article

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