Dulbecco R, Armstrong B
Monoclonal Antibody Laboratory of the Armand Hammer Cancer Center, Salk Institute, San Diego, CA 92138.
Proc Natl Acad Sci U S A. 1988 Nov;85(22):8659-63. doi: 10.1073/pnas.85.22.8659.
We have studied the progression of breast tumors induced by N-methyl-N-nitrosourea in Wistar/Furst rats during serial passages through isogeneic animals, using characteristic markers previously defined. The tumors contained various types of structure, which evolve from intraductal nodes to duct-like structures and then to invasive strands or cells. Most primary tumors were not invasive but became so in subsequent transfers. The distribution of invasive and noninvasive tumors in the various lineages was not random, implying that the tumors differed from their inception in the propensity toward invasion. In different lineages invasive structures appeared repeatedly and independently but with different frequencies, suggesting that they were produced by a stochastic mechanism with different probability of occurrence. The possible nature of this mechanism is discussed. This experimental system is useful for further studies of tumor invasion; the results obtained are relevant for understanding and evaluating the evolution of human breast cancer.
我们利用先前定义的特征性标志物,研究了N-甲基-N-亚硝基脲诱导的Wistar/Furst大鼠乳腺肿瘤在同基因动物中连续传代过程中的进展情况。肿瘤包含多种类型的结构,从导管内结节演变为导管样结构,然后发展为浸润性条索或细胞。大多数原发性肿瘤无浸润性,但在随后的传代中会出现浸润性。不同谱系中浸润性和非浸润性肿瘤的分布并非随机,这意味着肿瘤从一开始就存在侵袭倾向的差异。在不同谱系中,浸润性结构反复独立出现,但频率不同,这表明它们是由发生概率不同的随机机制产生的。本文讨论了该机制的可能性质。这个实验系统有助于进一步研究肿瘤侵袭;所获得的结果对于理解和评估人类乳腺癌的演变具有重要意义。