A new approach for estimating the progression of pancreatic cancer

Shuhao Sun, F. Klebaner, Tianhai Tian
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引用次数: 5

Abstract

Cancer of the pancreas is a highly lethal disease and has an extremely poor prognosis. It is the fourth leading cause of death from cancer in the US and the twelfth worldwide. There are currently only few therapeutic options for patients with pancreatic cancer. Hence new insights into the pathogenesis of this lethal disease are urgently needed. In recent years, extensive biological research has been conducted to study the mechanisms that control the initiation and progression of pancreas cancer. Mathematical models have also been used to present quantitative analysis and predict reasonable time schemes for the progression of pancreatic cancer. However, in those published articles, it was assumed that the mutation rate was constant, which is not realistic. In this work, we present a new approach using non-constant mutation rate and hence reveal several important biological parameters of cancer progression, such as initial mutation rate as well as doubling time (or selective advantage coefficients) in different stages, and eventually present a better time scheme. Under more realistic assumptions regarding gene mutation and a more reasonable mutation rate, the averaged values of doubling time and selective advantage coefficient generated by our model are consistent with the predictions made by the published models.
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估计胰腺癌进展的新方法
胰腺癌是一种高度致命的疾病,预后极差。它是美国第四大癌症死亡原因,也是全球第12大癌症死亡原因。目前胰腺癌患者的治疗选择很少。因此,迫切需要对这种致命疾病的发病机制有新的认识。近年来,人们进行了大量的生物学研究,以研究控制胰腺癌发生和发展的机制。数学模型也被用于提供定量分析和预测胰腺癌进展的合理时间方案。然而,在那些发表的文章中,假设突变率是恒定的,这是不现实的。在这项工作中,我们提出了一种使用非恒定突变率的新方法,从而揭示了癌症进展的几个重要生物学参数,如初始突变率以及不同阶段的加倍时间(或选择优势系数),并最终提出了一个更好的时间方案。在更现实的基因突变假设和更合理的突变率下,我们的模型得到的加倍时间和选择优势系数的平均值与已有模型的预测一致。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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