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首页> 外文期刊>Mathematical Biosciences: An International Journal >Characterizing inhibited tumor growth in stem-cell-driven non-spatial cancers
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Characterizing inhibited tumor growth in stem-cell-driven non-spatial cancers

机译:在干细胞驱动的非空间癌症中表征抑制的肿瘤生长

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摘要

Healthy human tissue is highly regulated to maintain homeostasis. Secreted negative feedback factors that inhibit stem cell division and stem cell self-renewal play a fundamental role in establishing this control. The appearance of abnormal cancerous growth requires an escape from these regulatory mechanisms. In a previous study we found that for non-solid tumors if feedback inhibition on stem cell self-renewal is lost, but the feedback on the division rate is still intact, then the tumor dynamics are characterized by a relatively slow sub-exponential growth that we called inhibited growth. Here we characterize the cell dynamics of inhibited cancer growth by modeling feedback inhibition using Hill equations. We find asymptotic approximations for the growth rates of the stem cell and differentiated cell populations in terms of the strength of the inhibitory signal: stem cells grow as a power law t(1/k+1), and the differentiated cells grow as OM, where k is the Hill coefficient in the feedback law regulating cell divisions. It follows that as the tumor grows, undifferentiated cells take up an increasingly large fraction of the population. Implications of these results for specific cancers including CML are discussed. Understanding how the regulatory mechanisms that continue to operate in cancer affect the rate of disease progression can provide important insights relevant to chronic or other slow progressing types of cancer. (C) 2015 Elsevier Inc. All rights reserved.
机译:健康的人体组织受到严格调节以维持体内平衡。抑制干细胞分裂和干细胞自我更新的分泌的负反馈因子在建立这种控制中起着根本性的作用。异常的癌症生长的出现需要摆脱这些调节机制。在先前的研究中,我们发现对于非实体瘤,如果丧失了对干细胞自我更新的反馈抑制作用,但对分裂速率的反馈仍然完好无损,则肿瘤动力学的特征在于相对缓慢的亚指数生长,即我们称之为抑制增长。在这里,我们通过使用Hill方程对反馈抑制进行建模来表征抑制的癌症生长的细胞动力学。根据抑制信号的强度,我们发现了干细胞和分化细胞群的增长率的渐近近似值:干细胞随着幂律t(1 / k + 1)增长,而分化细胞随着OM增长,其中,k是调节细胞分裂的反馈定律中的希尔系数。因此,随着肿瘤的生长,未分化的细胞占据了越来越大的比例。讨论了这些结果对包括CML在内的特定癌症的影响。了解继续在癌症中起作用的调节机制如何影响疾病的进展速度,可以提供与慢性或其他缓慢进展的癌症类型相关的重要见解。 (C)2015 Elsevier Inc.保留所有权利。

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