Dulbecco R, Armstrong B, Allen R
Monoclonal Antibody Laboratory, Armand Hammer Cancer Center, Salk Institute, San Diego, CA 92138.
Proc Natl Acad Sci U S A. 1988 Dec;85(23):9292-6. doi: 10.1073/pnas.85.23.9292.
To work toward an understanding of the mechanisms of cancer progression, we have followed the changes in expression of several genes in rat mammary carcinomas during the development of invasion. Tumors were induced by N-methyl-N-nitrosourea and serially transplanted to isogeneic rats. Gene expression in individual cells was followed by immunofluorescence microscopy. We show that invading cells do not express the same genes as the primary tumor or normal adult mammary gland but are similar to the primitive mammary duct cells present in late embryos. In the most advanced tumors, the most fundamental epithelial characteristic, polarity, is lost. Relative to the mechanism of invasion, we observe that the basal lamina, often thinner than normal, always coats the strands of invading cells and may be entirely absent from single invasive cells only. These observations suggest that the basal lamina ultimately disappears because of reduced expression of the genes or the failure to assemble the components. In these tumors it is the progressive alteration in gene expression rather than the enzymatic breakdown of the basal lamina that leads to invasion. These results show that the most important aspect of cancer progression is the progressive alteration of gene expression. They also raise questions about the mechanism that causes tumor cells to retrace the steps in their differentiation.
为了深入了解癌症进展的机制,我们追踪了大鼠乳腺癌在侵袭过程中几种基因表达的变化。通过N-甲基-N-亚硝基脲诱导肿瘤,并将其连续移植到同基因大鼠体内。利用免疫荧光显微镜观察单个细胞中的基因表达。我们发现,侵袭细胞所表达的基因与原发性肿瘤或正常成年乳腺组织不同,而是类似于晚期胚胎中存在的原始乳腺导管细胞。在最晚期的肿瘤中,最基本的上皮特征——极性丧失。关于侵袭机制,我们观察到,基底膜通常比正常的薄,总是覆盖着侵袭细胞束,并且可能仅在单个侵袭细胞中完全缺失。这些观察结果表明,基底膜最终消失是由于基因表达减少或未能组装其成分。在这些肿瘤中,是基因表达的渐进性改变而非基底膜的酶解导致了侵袭。这些结果表明,癌症进展的最重要方面是基因表达的渐进性改变。它们还引发了关于导致肿瘤细胞回溯其分化步骤的机制的问题。