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细胞在培养中的转化动力学及其对动物肿瘤发生的意义。

Dynamics of cell transformation in culture and its significance for tumor development in animals.

机构信息

Department of Molecular and Cell Biology, University of California, Berkeley, CA 94720-3200

出版信息

Proc Natl Acad Sci U S A. 2017 Nov 14;114(46):12237-12242. doi: 10.1073/pnas.1715236114. Epub 2017 Oct 30.

Abstract

NIH 3T3 cells grown in conventional Dulbecco's modification of Eagle's basal medium (DME) produce no transformed foci when grown to confluence in 10% calf serum (CS). A few cultures were transformed by ras oncogenes when transfected with DNA from neoplastic cells, but they failed to do so in 80 to 90% of the transfections. However, when they were grown in a medium [molecular, cellular, and developmental biology 402 (MCDB 402)] optimized for their clonal growth in minimal serum, they produced transformed foci without transfection in 10% CS, but not in 2% CS. The first response to growth in MCDB 402 in 2% CS in successive rounds of contact inhibition was uniform increases in saturation density of the population. This was followed by the appearance of transformed foci. A systematic study was made of the dynamics of neoplastic progression in various concentrations of CS in a single round of confluence at 2 and 3 wk, followed by three sequential rounds of confluence in 2% CS for 2 wk. There was a linear relationship between CS concentration and saturation density in the first-round cultures and continuing differences in subsequent cultures. The hyperplastic field of normal-looking cells surrounding transformed foci became increasingly permissive for transformation with serial culture. The dynamics show that epigenetic selection is the major driving force of neoplastic development. Cells from dense foci produced malignant fibrosarcomas in mice, thereby exhibiting a positive relationship between transformation in culture and the development of tumors.

摘要

在常规的 Eagle 氏基础培养基(DME)中生长的 NIH 3T3 细胞在 10%小牛血清(CS)中生长到汇合时不会产生转化灶。当用来自肿瘤细胞的 DNA 转染时,少数培养物被 ras 癌基因转化,但在 80%到 90%的转染中它们未能转化。然而,当它们在一种优化的培养基(分子、细胞和发育生物学 402(MCDB 402))中生长时,该培养基有利于它们在最小血清浓度下的克隆生长,它们在 10%CS 中无需转染即可产生转化灶,但在 2%CS 中则不行。在连续轮次的接触抑制中,在 MCDB 402 中生长的第一个反应是群体的饱和密度均匀增加。随后出现转化灶。在一轮汇合中,在 2%CS 中进行了各种 CS 浓度的肿瘤进展动力学的系统研究,然后在 2%CS 中进行了三个连续轮次的汇合,持续 2 周。在第一轮培养物中,CS 浓度与饱和密度之间存在线性关系,而在随后的培养物中则存在持续的差异。正常外观细胞的增生场围绕转化灶变得越来越有利于连续培养的转化。动力学表明,表观遗传选择是肿瘤发展的主要驱动力。来自密集焦点的细胞在小鼠中产生恶性纤维肉瘤,从而在培养中的转化与肿瘤的发展之间表现出正相关关系。

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