Mathematical Modelling of Tumour Dormancy
نویسنده
چکیده
Many tumours undergo periods in which they apparently do not grow but remain at a roughly constant size for extended periods. This is termed tumour dormancy. The mechanisms responsible for dormancy include failure to develop an internal blood supply, individual tumour cells exiting the cell cycle and a balance between the tumour and the immune response to it. Tumour dormancy is of considerable importance in the natural history of cancer. In many cancers, and in particular in breast cancer, recurrence can occur many years after surgery to remove the primary tumour, following a long period of occult disease. Mathematical modelling suggested that continuous growth of tumours was incompatible with data of the times of recurrence in breast cancer, suggesting that tumour dormancy was a common phenomenon. Modelling has also been applied to understanding the mechanisms responsible for dormancy, how they can be manipulated and the implications for cancer therapy. Here, the literature on mathematical modelling of tumour dormancy is reviewed. In conclusion, promising future directions for research are discussed.
منابع مشابه
Oscillations and bistability in the dynamics of cytotoxic reactions mediated by the response of immune cells to solid tumours
In this paper, we study the competition between tumour progression due to cancer cell replication and tumour regression due to immune cell cytotoxicity. We show that the increase of specificity alone during the development of the immune response is not sufficient in general to reject the tumour. Moreover, we describe three distinct and independent mechanisms that can, in the absence of external...
متن کاملOn immunotherapies and cancer vaccination protocols: a mathematical modelling approach.
In this paper we develop a new mathematical model of immunotherapy and cancer vaccination, focusing on the role of antigen presentation and co-stimulatory signaling pathways in cancer immunology. We investigate the effect of different cancer vaccination protocols on the well-documented phenomena of cancer dormancy and recurrence, and we provide a possible explanation of why adoptive (i.e. passi...
متن کاملUniversity of Dundee Modelling and investigation of the CD4+ T cells-macrophages paradox in melanoma immunotherapies Eftimie, Raluca; Hamam, Haneen
It is generally accepted that tumour cells can be eliminated by M1 anti-tumour macrophages and CD8+ T cells. However, experimental results over the past 10–15 years have shown that B16 mouse melanoma cells can be eliminated by the CD4+ T cells alone (either Th1 or Th2 sub-types), in the absence of CD8+ T cells. In some studies, elimination of B16 melanoma was associated with a Th1 immune respon...
متن کاملMelanoma dormancy in a mouse model is linked to GILZ/FOXO3A-dependent quiescence of disseminated stem-like cells
Metastatic cancer relapses following the reactivation of dormant, disseminated tumour cells; however, the cells and factors involved in this reactivation are just beginning to be identified. Using an immunotherapy-based syngeneic model of melanoma dormancy and GFP-labelled dormant cell-derived cell lines, we determined that vaccination against melanoma prevented tumour growth but did not preven...
متن کاملIn Silico Modelling of Tumour Margin Diffusion and Infiltration: Review of Current Status
As a result of advanced treatment techniques, requiring precise target definitions, a need for more accurate delineation of the Clinical Target Volume (CTV) has arisen. Mathematical modelling is found to be a powerful tool to provide fairly accurate predictions for the Microscopic Extension (ME) of a tumour to be incorporated in a CTV. In general terms, biomathematical models based on a sequenc...
متن کامل