Delayed Onset of Symptoms Through Feedback Interference in Chronic Cancers.

Convergent science physical oncology Pub Date : 2016-01-01 Epub Date: 2016-10-21 DOI:10.1088/2057-1739/2/4/045002
Seth Haney, Tannishtha Reya, Maxim Bazhenov
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引用次数: 1

Abstract

In many cancers, such as Chronic Myelogenous Leukemia (CML), pancreatic, and colorectal cancer, long delays exist between the initiation of the disease and the onset of debilitating symptoms. The early stages of these diseases present manageable symptoms and, in the case of CML, highly effective treatment options. Progression to the more aggressive stages of the diseases limits effective treatment and significantly exacerbates patient prognosis. The mechanisms causing delay and disease progression are largely unknown. The later stages of these diseases are characterized by excessive build up of primitive cell types, indicating a disruption in the normal cell differentiation process that is commonly regulated through feedback from differentiated types. In this study, we propose a mechanism where mutated primitive cells produce a feedback interference signal that desensitizes them to a normal homeostatic feedback. Using a mathematical model, we show that this mechanism can account for the long delay period between occurrence of genetic changes and symptomatic onset characterized by fast growth of cancerous cell population. Finally, we explore novel concepts for potential treatment of chronic cancers.

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通过反馈干扰延缓慢性癌症症状的发作。
在许多癌症中,如慢性骨髓性白血病(CML)、胰腺癌和结直肠癌,在发病和出现衰弱症状之间存在很长时间的延迟。这些疾病的早期阶段表现出可控的症状,在慢性粒细胞白血病的情况下,有非常有效的治疗方案。疾病进展到更严重的阶段限制了有效的治疗,并显著恶化了患者的预后。导致延迟和疾病进展的机制在很大程度上是未知的。这些疾病的后期阶段的特点是原始细胞类型的过度建立,表明正常细胞分化过程的中断,通常通过分化类型的反馈来调节。在这项研究中,我们提出了一种机制,突变的原始细胞产生反馈干扰信号,使它们对正常的稳态反馈脱敏。利用数学模型,我们发现这种机制可以解释遗传变化的发生和以癌细胞群快速生长为特征的症状发作之间的长延迟期。最后,我们探讨了慢性癌症潜在治疗的新概念。
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