FAILURE OF PROGRAMMED CELL-DEATH AND DIFFERENTIATION AS CAUSES OF TUMORS - SOME SIMPLE MATHEMATICAL-MODELS

被引:158
作者
TOMLINSON, IPM
BODMER, WF
机构
[1] Cancer Genetics Laboratory, Imperial Cancer Research Fund, London WC2A 3PX
关键词
TUMORIGENESIS; APOPTOSIS;
D O I
10.1073/pnas.92.24.11130
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Most models of tumorigenesis assume that the tumor grows by increased cell division. In these models, it is generally supposed that daughter cells behave as do their parents, and cell numbers have clear potential for exponential growth. We have constructed simple mathematical models of tumorigenesis through failure of programmed cell death (PCD) or differentiation. These models do not assume that descendant cells behave as their parents do. The models predict that exponential growth in cell numbers does sometimes occur, usually when stem cells fail to die or differentiate. At other times, exponential growth does not occur: instead, the number of cells in the population reaches a new, higher equilibrium. This behavior is predicted when fully differentiated cells fail to undergo PCD. When cells of intermediate differentiation fail to die or to differentiate further, the values of growth parameters determine whether growth is exponential or leads to a new equilibrium. The predictions of the model are sensitive to small differences in growth parameters. Failure of PCD and differentiation, leading to a new equilibrium number of cells, may explain many aspects of tumor behavior-for example, early premalignant lesions such as cervical intraepithelial neoplasia, the fact that some tumors very rarely become malignant, the observation of plateaux in the growth of some solid tumors, and, finally, long lag phases of growth until mutations arise that eventually result in exponential growth.
引用
收藏
页码:11130 / 11134
页数:5
相关论文
共 21 条
  • [1] THE AGE DISTRIBUTION OF CANCER AND A MULTI-STAGE THEORY OF CARCINOGENESIS
    ARMITAGE, P
    DOLL, R
    [J]. BRITISH JOURNAL OF CANCER, 1954, 8 (01) : 1 - 12
  • [2] A 2-STAGE THEORY OF CARCINOGENESIS IN RELATION TO THE AGE DISTRIBUTION OF HUMAN CANCER
    ARMITAGE, P
    DOLL, R
    [J]. BRITISH JOURNAL OF CANCER, 1957, 11 (02) : 161 - 169
  • [3] P53 BINDS SINGLE-STRANDED-DNA ENDS AND CATALYZES DNA RENATURATION AND STRAND TRANSFER
    BAKALKIN, G
    YAKOVLEVA, T
    SELIVANOVA, G
    MAGNUSSON, KP
    SZEKELY, L
    KISELEVA, E
    KLEIN, G
    TERENIUS, L
    WIMAN, KG
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (01) : 413 - 417
  • [4] MUTATION SELECTION AND NATURAL-HISTORY OF CANCER
    CAIRNS, J
    [J]. NATURE, 1975, 255 (5505) : 197 - 200
  • [5] THYMOCYTE APOPTOSIS INDUCED BY P53-DEPENDENT AND INDEPENDENT PATHWAYS
    CLARKE, AR
    PURDIE, CA
    HARRISON, DJ
    MORRIS, RG
    BIRD, CC
    HOOPER, ML
    WYLLIE, AH
    [J]. NATURE, 1993, 362 (6423) : 849 - 852
  • [6] THE TUMOR-SUPPRESSOR P53
    DONEHOWER, LA
    BRADLEY, A
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA, 1993, 1155 (02) : 181 - 205
  • [7] INDUCTION OF APOPTOSIS IN FIBROBLASTS BY C-MYC PROTEIN
    EVAN, GI
    WYLLIE, AH
    GILBERT, CS
    LITTLEWOOD, TD
    LAND, H
    BROOKS, M
    WATERS, CM
    PENN, LZ
    HANCOCK, DC
    [J]. CELL, 1992, 69 (01) : 119 - 128
  • [8] FANADI A, 1992, NATURE, V359, P554
  • [9] APOPTOSIS IN CANCER-THERAPY - CROSSING THE THRESHOLD
    FISHER, DE
    [J]. CELL, 1994, 78 (04) : 539 - 542
  • [10] MULTIPLE-MUTATION THEORY OF CARCINOGENESIS
    FISHER, JC
    [J]. NATURE, 1958, 181 (4609) : 651 - 652