The microenvironments of multistage carcinogenesis

被引:43
作者
Laconi, Ezio [1 ]
Doratiotto, Silvia [1 ]
Vineis, Paolo [2 ]
机构
[1] Univ Cagliari, Dipartimento Sci & Tecnol Biomed, Sez Patol Sperimentale, I-09125 Cagliari, Italy
[2] Univ London Imperial Coll Sci Technol & Med, Dept Epidemiol & Publ Hlth, London W2 1PG, England
关键词
carcinogenesis;
D O I
10.1016/j.semcancer.2008.03.019
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Overt neoplasia is often the result of a chronic disease process encompassing an extended segment of the lifespan of any species. A common pathway in the natural history of the disease is the appearance of focal proliferative lesions that are known to act as precursors for cancer development. It is becoming increasingly apparent that the emergence of such lesions is not a cell-autonomous phenomenon, but is heavily dependent on microenvironmental cues derived from the surrounding tissue. Specific alterations in the tissue microenvironment that can foster the selective growth of focal lesions are discussed herein. Furthermore, we argue that a fundamental property of focal lesions as it relates to their precancerous nature lies in their altered growth pattern as compared to the tissue where they reside. The resulting altered tissue architecture translates into the emergence of a unique tumor microenvironment inside these lesions, associated with altered blood vessels and/or blood supply which in turn can trigger biochemical and metabolic changes fueling tumor progression. A deeper understanding of the role(s) of tissue and tumor microenvironments in the pathogenesis of cancer is essential to design more effective strategies for the management of this disease. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:322 / 329
页数:8
相关论文
共 110 条
  • [41] HALL BG, 1990, GENETICS, V126, P5
  • [42] HANIGAN MH, 1985, CANCER RES, V45, P6063
  • [43] Neoplastic precursor lesions related to the development of cancer in inflammatory bowel disease
    Harpaz, Noam
    [J]. GASTROENTEROLOGY CLINICS OF NORTH AMERICA, 2007, 36 (04) : 901 - +
  • [44] Harris RS, 1999, MUTAT RES-REV MUTAT, V437, P51
  • [45] Hypoxia-induced genetic instability - a calculated mechanism underlying tumor progression
    Huang, L. Eric
    Bindra, Ranjit S.
    Glazer, Peter M.
    Harris, Adrian L.
    [J]. JOURNAL OF MOLECULAR MEDICINE-JMM, 2007, 85 (02): : 139 - 148
  • [46] Inflammation and cancer: An ancient link with novel potentials
    Hussain, S. Perwez
    Harris, Curtis C.
    [J]. INTERNATIONAL JOURNAL OF CANCER, 2007, 121 (11) : 2373 - 2380
  • [47] Hussain SP, 2001, CANCER RES, V61, P6350
  • [48] ON THE CLONAL ORIGIN OF TUMORS - A REVIEW OF EXPERIMENTAL-MODELS
    IANNACCONE, PM
    WEINBERG, WC
    DEAMANT, FD
    [J]. INTERNATIONAL JOURNAL OF CANCER, 1987, 39 (06) : 778 - 784
  • [49] The impact of donor age on living donor liver transplantation
    Ikegami, T
    Nishizaki, T
    Yanaga, K
    Shimada, M
    Kishikawa, K
    Nomoto, K
    Uchiyama, H
    Sugimachi, K
    [J]. TRANSPLANTATION, 2000, 70 (12) : 1703 - 1707
  • [50] Can cancer be reversed by engineering the tumor microenvironment?
    Ingber, Donald E.
    [J]. SEMINARS IN CANCER BIOLOGY, 2008, 18 (05) : 356 - 364