C38结肠腺癌和B16黑色素瘤肿瘤生长模型的鉴定与分析

Johanna Sápi, D. Drexler, I. Harmati, A. Szeles, B. Kiss, Z. Sápi, L. Kovács
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引用次数: 8

摘要

抗癌治疗正在扩大,一种有前途的类型,靶向分子治疗有了新的方法。这些疗法的目的不是消灭整个肿瘤,而是将肿瘤控制在一个给定的状态,并使其保持在那里。明确了解肿瘤生长动力学和靶向分子治疗的效果对肿瘤治疗的发展至关重要。我们展示了在C38结肠腺癌和B16黑色素瘤的情况下研究肿瘤生长的小鼠实验结果。拟合了几条曲线,并检查了肿瘤生长动力学。测量肿瘤的三个属性:肿瘤体积、肿瘤质量和血管化;观察肿瘤生长动态。用数字卡尺测量肿瘤体积,冷冻切片用CD31抗体免疫组化染色观察血管形成。用线性回归分析检验这些肿瘤属性之间的关系。肿瘤生长动力学被确定为一个二阶线性系统。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Tumor growth model identification and analysis in case of C38 colon adenocarcinoma and B16 melanoma
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.
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