Pollack R E, Kopelovich L
Methods Achiev Exp Pathol. 1979;9:207-30.
Adenopolyposis of the colon and rectum (ACR) links the well-characterized phenomena of murine oncogenic virus transformation with the progression of a human cancer. The same syndrome links defects in fibroblast growth control and cytoskeletal organization to a tumor of epithelial origin. Since skin fibroblasts are involved in this colonic tumor, the syndrome is very likely to be systemic. That is, one element of normal growth regulation of epithelial cells in situ may be provided by the fibroblasts residing beneath their basement membrane. These observations have led to a novel approach to early detection of persons at risk for a tumor, via the behavior of their skin fibroblasts in culture. At present, it is rarely possible to detect persons at risk for malignancy before the appearance of a frank invasive or metastatic growth. Although many biochemical assays have been proposed as indicators of pre-malignant states or cryptic early tumors, most have eventually been shown to be related to age, sex drug treatment, or other variables linked to but not clearly indicative of, a malignancy. Two serious problems limiting attempts to detect preneoplastic states or a disposition to eventual neoplasia are the inherent low frequency of incidence of any single type of tumor and the difficulty of obtaining identical sample material from prospective or actual patients once they are located. Our approach to these problems significantly departs from the common dependence upon isolation of cells from the site of a tumor. Clearly, it is an easier task to scan skin fibroblasts for disrupted cytoskeletal patterns than it is to obtain epithelia cells from most tissues at high risk for malignancy. This line of work, buttressed by information derived from the model system of SV40 transformation, may provide a novel mode of early detection of other human malignancies, as it has for ACR.
结肠和直肠腺瘤性息肉病(ACR)将小鼠致癌病毒转化这一特征明确的现象与人类癌症的进展联系起来。同一综合征还将成纤维细胞生长控制和细胞骨架组织的缺陷与上皮起源的肿瘤联系起来。由于皮肤成纤维细胞与这种结肠肿瘤有关,该综合征很可能是全身性的。也就是说,原位上皮细胞正常生长调节的一个要素可能由位于其基底膜下方的成纤维细胞提供。这些观察结果导致了一种通过培养皮肤成纤维细胞的行为来早期检测有肿瘤风险人群的新方法。目前,在出现明显的侵袭性或转移性生长之前,很少有可能检测出有恶性肿瘤风险的人群。尽管已经提出了许多生化检测方法作为癌前状态或隐匿性早期肿瘤的指标,但大多数最终都被证明与年龄、性别、药物治疗或其他与恶性肿瘤相关但不明确指示恶性肿瘤的变量有关。限制检测癌前状态或最终发生肿瘤倾向的尝试的两个严重问题是任何单一类型肿瘤固有的低发病率,以及一旦找到潜在或实际患者,从他们身上获取相同样本材料的困难。我们解决这些问题的方法与通常依赖从肿瘤部位分离细胞的方法有很大不同。显然,扫描皮肤成纤维细胞的细胞骨架模式紊乱比从大多数有恶性肿瘤高风险的组织中获取上皮细胞要容易得多。这项工作得到了来自SV40转化模型系统的信息的支持,可能会为其他人类恶性肿瘤提供一种新的早期检测模式,就像它对ACR所做的那样。