Abstract

Cancer chemoresistance (including adaptive resistance) has emerged as a barrier in developing successful chemotherapeutic strategies. We use Monte Carlo simulation based single cell analysis to provide insights into the regulatory mechanisms for generating chemoresistance under TRAIL (death ligand) induction. Based on stochastic computer simulations we elucidate systems biology of cancer cell apoptosis (at the level of single cells) and search for an optimal death ligand from a group of recently studied TRAIL affinity variants. In addition to assessing the population level behavior in cell death activation under induction of TRAIL/TRAIL-variant, Monte Carlo approach allows us to analyze cell-to-cell stochastic fluctuations in time-to-death that has implications for generating resistant cancer cells. We discuss application of Monte Carlo simulations in the context of developing more personalized approaches in treating various cancers. Initial findings indicate single cell in silico approaches can be utilized for disease subtype classification and in characterizing a given tumor, and, for finding an optimal strategy (such as network modules to target and ligands needed) in targeting a given tumor.

Highlights

  • Resistance to apoptotic cell death is a defining feature of malignant phenotype in cancer cells

  • In this article, based on our ongoing effort in studying single cell biology of apoptosis induction by various chemotherapeutic agents, we report potential applications of stochastic simulations in developing effective cancer therapy

  • Based on recent experimental studies of apoptotic activation induced by affinity variant ligands [15,16], we carry out Monte Carlo simulation of apoptotic activation for two such altered ligands (DR5A and DR5B) in death receptor 5 expressing cancer cells [16]

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Summary

Introduction

Resistance to apoptotic cell death is a defining feature of malignant phenotype in cancer cells. We have engaged in developing Monte Carlo models that started elucidating the mechanisms for TRAIL induced bimodal apoptotic activation (of purely stochastic kinetic origin [14]) leading to fractional cell killing and generation of resistant phenotypes.

Results
Conclusion

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