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Mathematical model of colitis-associated colon cancer
被引:4
|作者:
Lo, Wing-Cheong
[1
]
Martin, Edward W., Jr.
[2
,3
,4
]
Hitchcock, Charles L.
[5
]
Friedman, Avner
[1
,6
]
机构:
[1] Ohio State Univ, Math Biosci Inst, Columbus, OH 43210 USA
[2] Ohio State Univ, Arthur G James Canc Hosp, Dept Surg, Div Surg Oncol, Columbus, OH 43210 USA
[3] Ohio State Univ, Richard J Solove Res Inst, Columbus, OH 43210 USA
[4] Ohio State Univ, Ctr Comprehens Canc, Columbus, OH 43210 USA
[5] Ohio State Univ, Dept Pathol, Columbus, OH 43210 USA
[6] Ohio State Univ, Dept Math, Columbus, OH 43210 USA
基金:
美国国家科学基金会;
关键词:
Colorectal cancer;
Mucin;
APC;
TP53;
Mathematical model;
NF-KAPPA-B;
BETA-CATENIN;
ALTERED DISTRIBUTION;
COLORECTAL-CANCER;
BINDING-PROTEINS;
MUCIN DYNAMICS;
GENE;
APC;
ACTIVATION;
INFLAMMATION;
D O I:
10.1016/j.jtbi.2012.09.025
中图分类号:
Q [生物科学];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
As a result of chronic inflammation of their colon, patients with ulcerative colitis or Crohn's disease are at risk of developing colon cancer. In this paper, we consider the progression of colitis-associated colon cancer. Unlike normal colon mucosa, the inflammed colon mucosa undergoes genetic mutations, affecting, in particular, tumor suppressors TP53 and adenomatous polyposis coli (APC) gene. We develop a mathematical model that involves these genes, under chronic inflammation, as well as NF-kappa B, beta-catenin, MUC1 and MUC2. The model demonstrates that increased level of cells with TP53 mutations results in abnormal growth and proliferation of the epithelium; further increase in the epithelium proliferation results from additional APC mutations. The model may serve as a conceptual framework for further data-based study of the early stage of colon cancer. (C) 2012 Elsevier Ltd. All rights reserved.
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页码:20 / 29
页数:10
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