Papadimitrakopoulou V A, Shin D M, Hong W K
Department of Thoracic/Head and Neck Medical Oncology, University of Texas M.D. Anderson Cancer Center, Houston 77030, USA.
Cancer Metastasis Rev. 1996 Mar;15(1):53-76. doi: 10.1007/BF00049487.
One way to explain the development of head and neck cancer is through the theories of field cancerization, i.e., the exposure of an entire field of tissue to repeated carcinogenic insult, and multistep process, i.e., development of multiple cancers in a predisposed filed through a series of recognizable stages. Recent molecular genetic studies of histologically normal and premalignant epithelia of high-risk subjects and studies of malignant tumors in aerodigestive tract epithelia have identified a continuum of accumulated specific genetic alterations that possibly occur during the clonal evolution of tumors, namely, during the multistep process. Second primary or multiple primary tumors arise in the same fields as independent clones, with similar but unique molecular genetic and/or cellular alterations. Consequently, the assessment of these genetic and phenotypic alterations has been integrated into clinical chemoprevention trials in an effort to identify biomarkers that are also risk predictors and intermediate end points. This review covers candidate biomarkers of the processes of field cancerization and multistep tumor development in aerodigestive tract epithelia, including general and specific genetic markers, proliferation markers, and squamous differentiation markers.
解释头颈癌发展的一种方式是通过场癌化理论,即整个组织场暴露于反复的致癌性损伤,以及多步骤过程,即在易感区域通过一系列可识别的阶段发展出多种癌症。近期对高危受试者组织学正常和癌前上皮的分子遗传学研究以及对气道消化道上皮恶性肿瘤的研究,已经确定了在肿瘤克隆进化过程中可能发生的一系列累积的特定基因改变,即在多步骤过程中。第二原发性或多发性原发性肿瘤在相同区域作为独立克隆出现,具有相似但独特的分子遗传学和/或细胞改变。因此,对这些基因和表型改变的评估已被纳入临床化学预防试验,以努力识别同时也是风险预测指标和中间终点的生物标志物。本综述涵盖了气道消化道上皮场癌化和肿瘤多步骤发展过程的候选生物标志物,包括一般和特定的基因标志物、增殖标志物和鳞状分化标志物。