Broad Institute, Cambridge, MA 02142, USA.
Cell. 2011 Aug 19;146(4):633-44. doi: 10.1016/j.cell.2011.07.026.
Cancer cells within individual tumors often exist in distinct phenotypic states that differ in functional attributes. While cancer cell populations typically display distinctive equilibria in the proportion of cells in various states, the mechanisms by which this occurs are poorly understood. Here, we study the dynamics of phenotypic proportions in human breast cancer cell lines. We show that subpopulations of cells purified for a given phenotypic state return towards equilibrium proportions over time. These observations can be explained by a Markov model in which cells transition stochastically between states. A prediction of this model is that, given certain conditions, any subpopulation of cells will return to equilibrium phenotypic proportions over time. A second prediction is that breast cancer stem-like cells arise de novo from non-stem-like cells. These findings contribute to our understanding of cancer heterogeneity and reveal how stochasticity in single-cell behaviors promotes phenotypic equilibrium in populations of cancer cells.
肿瘤内的癌细胞通常存在于不同功能属性的独特表型状态中。虽然癌细胞群体通常在不同状态的细胞比例上表现出明显的平衡,但这种情况发生的机制尚不清楚。在这里,我们研究了人类乳腺癌细胞系中表型比例的动态变化。我们表明,纯化特定表型状态的细胞亚群会随着时间的推移而恢复到平衡比例。这些观察结果可以用一个马尔可夫模型来解释,其中细胞在状态之间随机转换。该模型的一个预测是,在某些条件下,任何细胞亚群都会随着时间的推移恢复到平衡的表型比例。第二个预测是,乳腺癌类干细胞是从头从非类干细胞中产生的。这些发现有助于我们理解癌症异质性,并揭示了单细胞行为的随机性如何促进癌细胞群体中表型平衡。