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Tumor growth model identification and analysis in case of C38 colon adenocarcinoma and B16 melanoma

机译:C38结肠腺癌和B16黑色素瘤的肿瘤生长模型鉴定与分析

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Cancer fighting treatments are expanding, and a promising type, targeted molecular therapies have a new approach. The aim of these therapies is not to eliminate the whole tumor, but to control the tumor into a given state and keep it there. Explicit knowledge of tumor growth dynamics and the effects of targeted molecular therapies is crucial in tumor treatment development. We show the results of mouse experiments where tumor growth was investigated in case of C38 colon adenocarcinoma and B16 melanoma. Several curves were fitted and tumor growth dynamics was examined. Three attributes of tumor were measured: tumor volume, tumor mass and vascularization; and tumor growth dynamics was examined. Tumor volume was measured with digital caliper, vascularization was investigated with CD31 antibody immunohistochemistry staining on frozen sections. The relationship between these tumor attributes were examined with linear regression analysis. The dynamics of tumor growth was identified as a second order linear system.
机译:癌症的治疗方法正在扩大,一种有前途的靶向分子疗法有了新的方法。这些疗法的目的不是消除整个肿瘤,而是将肿瘤控制在给定状态并将其保持在那里。明确了解肿瘤生长动力学和靶向分子疗法的作用对于肿瘤治疗的发展至关重要。我们显示了小鼠实验的结果,其中在C38结肠腺癌和B16黑色素瘤的情况下研究了肿瘤的生长。拟合了几条曲线并检查了肿瘤生长动力学。测量了肿瘤的三个属性:肿瘤体积,肿瘤质量和血管化;并检查了肿瘤的生长动力学。用数字卡尺测量肿瘤体积,在冷冻切片上用CD31抗体免疫组织化学染色研究血管形成。用线性回归分析检查这些肿瘤属性之间的关系。肿瘤生长的动力学被确定为二阶线性系统。

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