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A Mathematical Modelling for Estradiol Influence on DNA Damage Response and G1/S Transition Phase Regulations in Early Stage of Breast Cancer

机译:雌二醇对乳腺癌早期DNA损伤反应和G1 / S转变阶段规范的数学建模

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Breast cancer is a malignant disease that triggers the anomalies of the cells proliferation in breast tissue. There are some known factors that have ability to increase someone risk to suffer this disease, i.e., hormone, genetics, lifestyle, etc. One of the important hormone for the growth of breast tissue is estrogen, but it also contributes to breast cancer via DNA damage induced by producing the oxidative metabolites. Also, estrogen can provoke excessive proliferation that triggers the tumorigenesis process, where the key effectors are C-Myc and Cyclin D1 (CycDl). In this paper, we introduce a new mathematical model of the DNA damage as the response of the estrogen involving the Gl/S transition phase in cell cycle. The model is a 15-dimensional system of the first order of ODE that shows the chemical reactions between proteins and hormones that play important roles in cell cycle regulations. The model could be a foundation to understand the initial behavior of the breast cancer. We use numerical simulations by using fourth order Runge Kutta method to study the molecular behavior of the normal cells and the anomalies on the abnormal cells that initially lead breast cancer.
机译:乳腺癌是一种恶性疾病,触发了乳腺组织中细胞增殖的异常。有一些已知因素可以增加患有这种疾病的风险,即激素,遗传学,生活方式等。乳腺组织生长的重要激素之一是雌激素,但它也通过DNA促进乳腺癌通过产生氧化代谢物诱导的损伤。此外,雌激素可以引发过量的增殖,触发肿瘤发生过程,其中关键效应是C-MYC和细胞周期蛋白D1(CYCDL)。在本文中,我们将DNA损伤的新数学模型引入了涉及细胞周期中GL / S转化相的雌激素的响应。该模型是第一顺序的15维系统,其赋予蛋白质和激素之间的化学反应,这些反应在细胞周期法规中起重要作用。该模型可能是理解乳腺癌初始行为的基础。我们使用使用数值模拟来使用第四阶runge kutta方法来研究正常细胞和异常细胞上最初引入乳腺癌的异常的分子行为。

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