Pinsky P F
Division of Cancer Prevention, National Cancer Institute, Bethesda, MD, USA.
J Theor Biol. 2000 Nov 21;207(2):129-43. doi: 10.1006/jtbi.2000.2148.
The overwhelming proportion of colorectal carcinomas are believed to originate as adenomatous polyps (adenomas), and the identification and removal of adenomas is an important component of colorectal cancer prevention efforts. Mathematical modeling of adenomas can increase our understanding of the natural history and biology of adenomas and colorectal cancer and can help in the effort to devise optimal prevention and screening strategies. Here we adapt the multi-stage model of carcinogenesis to the problem of the development and growth of adenomas. We show that, using plausible values for the biological parameters, the model can fit various aspects of adenoma data including adenoma prevalence by age, the size distribution of adenomas, clustering of adenomas within individuals and the correlation between distal and proximal adenomas. Explaining the clustering of adenomas within individuals, as well as other findings, requires heterogeneity in risk in the population; we show how such heterogeneity can be related to the distribution of biological parameters in the population. The model can also be adapted to account for adenoma development in two major syndromes related to colorectal cancer, familial adenomatous polyposis and hereditary non-polyposis colorectal cancer.
绝大多数结直肠癌被认为起源于腺瘤性息肉(腺瘤),识别并切除腺瘤是结直肠癌预防工作的重要组成部分。腺瘤的数学建模可以增进我们对腺瘤以及结直肠癌自然史和生物学特性的理解,并有助于制定最佳的预防和筛查策略。在此,我们将多阶段致癌模型应用于腺瘤发生和生长的问题。我们表明,使用生物学参数的合理值时,该模型能够拟合腺瘤数据的各个方面,包括按年龄划分的腺瘤患病率、腺瘤的大小分布、个体内腺瘤的聚集情况以及远端和近端腺瘤之间的相关性。要解释个体内腺瘤的聚集情况以及其他发现,需要人群中存在风险异质性;我们展示了这种异质性如何与人群中生物学参数的分布相关。该模型还可进行调整,以解释与结直肠癌相关的两种主要综合征——家族性腺瘤性息肉病和遗传性非息肉病性结直肠癌中的腺瘤发生情况。