A Three-State Mathematical Model of Hyperthermic Cell Death

Thermal treatments for tissue ablation rely upon the heating of cells past a threshold beyond which the cells are considered destroyed, denatured, or killed. In this article, a novel three-state model for cell death is proposed where there exists a vulnerable state positioned between the alive and dead states used in a number of existing cell death models. Proposed rate coefficients include temperature dependence and the model is fitted to experimental data of heated co-cultures of hepatocytes and lung fibroblasts with very small RMS error. The experimental data utilized include further reductions in cell viabilities over 24 and 48 h post-heating and these data are used to extend the three-state model to account for slow cell death. For the two cell lines employed in the experimental data, the three parameters for fast cell death appear to be linearly increasing with % content of lung fibroblast, while the sparse nature of the data did not indicate any co-culture make-up dependence for the parameters for slow cell death. A critical post-heating cell viability threshold is proposed beyond which cells progress to death; and these results are of practical importance with potential for more accurate prediction of cell death.

[1]  Comparison of Two Mathematical Models for Hyperthermic Cell Death , 2010 .

[2]  J F Fowler,et al.  DIFFERENCES IN SURVIVAL CURVE SHAPES FOR FORMAL MULTI-TARGET AND MULTI-HIT MODELS , 1964 .

[3]  J. L. Roti,et al.  Comparison of two mathematical models for describing heat-induced cell killing. , 1980, Radiation research.

[4]  A. Moritz,et al.  Studies of Thermal Injury: III. The Pathology and Pathogenesis of Cutaneous Burns. An Experimental Study. , 1947, The American journal of pathology.

[5]  A. Moritz,et al.  Studies of Thermal Injury: I. The Conduction of Heat to and through Skin and the Temperatures Attained Therein. A Theoretical and an Experimental Investigation. , 1947, The American journal of pathology.

[6]  W. Telford,et al.  Spontaneous apoptosis and expression of cell surface heat‐shock proteins in cultured EL‐4 lymphoma cells , 1999, Cell proliferation.

[7]  A mathematical analysis of the results of experiments on rats' livers by local laser hyperthermia , 1989, Lasers in Medical Science.

[8]  A. Moritz,et al.  Studies of Thermal Injury: II. The Relative Importance of Time and Surface Temperature in the Causation of Cutaneous Burns. , 1947, The American journal of pathology.

[9]  J W Gray,et al.  Effects of hyperthermia on survival and progression of Chinese hamster ovary cells. , 1978, Cancer research.

[10]  M Birth,et al.  Influence of operator experience in radiofrequency ablation of malignant liver tumours on treatment outcome. , 2006, European journal of surgical oncology : the journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology.

[11]  S. Calderwood,et al.  TEMPERATURE RANGE AND SELECTIVE SENSITIVITY OF TUMORS TO HYPERTHERMIA: A CRITICAL REVIEW , 1980, Annals of the New York Academy of Sciences.

[12]  W. Dewey,et al.  Cell killing and the sequencing of hyperthermia and radiation. , 1979, International journal of radiation oncology, biology, physics.

[13]  John A Pearce,et al.  Models for thermal damage in tissues: processes and applications. , 2010, Critical reviews in biomedical engineering.

[14]  G. Dienes A kinetic model of biological radiation response. , 1966, Radiation research.

[15]  S T Clegg,et al.  Estimation of cell survival in tumours heated to nonuniform temperature distributions. , 1996, International journal of hyperthermia : the official journal of European Society for Hyperthermic Oncology, North American Hyperthermia Group.

[16]  H. Jung,et al.  A generalized concept for cell killing by heat. , 1986, Radiation research.

[17]  Michael S. Breen,et al.  Modeling cellular thermal damage from radio-frequency ablation , 2002, Proceedings of the Second Joint 24th Annual Conference and the Annual Fall Meeting of the Biomedical Engineering Society] [Engineering in Medicine and Biology.

[18]  H. Jung Step-down heating of CHO cells at 37.5-39 degrees C. , 1989, International Journal of Hyperthermia.

[19]  G S Gazelle,et al.  Percutaneous radiofrequency tissue ablation: optimization of pulsed-radiofrequency technique to increase coagulation necrosis. , 1999, Journal of vascular and interventional radiology : JVIR.

[20]  H. Jung A generalized concept for cell killing by heat. Effect of chronically induced thermotolerance. , 1991, Radiation research.

[21]  Yusheng Feng,et al.  A two-state cell damage model under hyperthermic conditions: theory and in vitro experiments. , 2008, Journal of biomechanical engineering.

[22]  D. Haines,et al.  Microwave catheter ablation of myocardium in vitro. Assessment of the characteristics of tissue heating and injury. , 1994, Circulation.

[23]  H. Arkin,et al.  Recent developments in modeling heat transfer in blood perfused tissues , 1994, IEEE Transactions on Biomedical Engineering.

[24]  N. Uchida,et al.  A model for cell killing by continuous heating. , 1993, Medical hypotheses.

[25]  A Szasz,et al.  Dose concept of oncological hyperthermia: heat-equation considering the cell destruction. , 2006, Journal of cancer research and therapeutics.

[26]  W. Dewey,et al.  Cellular responses to combinations of hyperthermia and radiation. , 1977, Radiology.

[27]  W. Dewey,et al.  Thermal dose determination in cancer therapy. , 1984, International journal of radiation oncology, biology, physics.

[28]  L. F. F. L-G Pathological Effects of Hyperthermia in Normal Tissues , 1984 .

[29]  Kenneth R Diller,et al.  Correlation of HSP70 expression and cell viability following thermal stimulation of bovine aortic endothelial cells. , 2005, Journal of biomechanical engineering.