Department of Medical Chemistry, Semmelweis University, P.O. Box 260, H-1444 Budapest 8, Hungary.
Department of Medical Chemistry, Semmelweis University, P.O. Box 260, H-1444 Budapest 8, Hungary.
Semin Cancer Biol. 2015 Feb;30:42-51. doi: 10.1016/j.semcancer.2013.12.004. Epub 2014 Jan 8.
Cancer is increasingly perceived as a systems-level, network phenomenon. The major trend of malignant transformation can be described as a two-phase process, where an initial increase of network plasticity is followed by a decrease of plasticity at late stages of tumor development. The fluctuating intensity of stress factors, like hypoxia, inflammation and the either cooperative or hostile interactions of tumor inter-cellular networks, all increase the adaptation potential of cancer cells. This may lead to the bypass of cellular senescence, and to the development of cancer stem cells. We propose that the central tenet of cancer stem cell definition lies exactly in the indefinability of cancer stem cells. Actual properties of cancer stem cells depend on the individual "stress-history" of the given tumor. Cancer stem cells are characterized by an extremely large evolvability (i.e. a capacity to generate heritable phenotypic variation), which corresponds well with the defining hallmarks of cancer stem cells: the possession of the capacity to self-renew and to repeatedly re-build the heterogeneous lineages of cancer cells that comprise a tumor in new environments. Cancer stem cells represent a cell population, which is adapted to adapt. We argue that the high evolvability of cancer stem cells is helped by their repeated transitions between plastic (proliferative, symmetrically dividing) and rigid (quiescent, asymmetrically dividing, often more invasive) phenotypes having plastic and rigid networks. Thus, cancer stem cells reverse and replay cancer development multiple times. We describe network models potentially explaining cancer stem cell-like behavior. Finally, we propose novel strategies including combination therapies and multi-target drugs to overcome the Nietzschean dilemma of cancer stem cell targeting: "what does not kill me makes me stronger".
癌症越来越被视为一种系统层面的网络现象。恶性转化的主要趋势可以描述为一个两阶段的过程,即网络可塑性的初始增加,随后在肿瘤发展的晚期降低。应激因素(如缺氧、炎症)的波动强度以及肿瘤细胞间网络的合作或敌对相互作用,都增加了癌细胞的适应潜力。这可能导致细胞衰老的旁路,并导致癌症干细胞的发展。我们提出,癌症干细胞定义的核心原则恰恰在于癌症干细胞的不可定义性。癌症干细胞的实际特性取决于特定肿瘤的个体“应激史”。癌症干细胞的特征是具有极高的可进化性(即产生可遗传表型变异的能力),这与癌症干细胞的定义特征非常吻合:具有自我更新和在新环境中反复重建构成肿瘤的异质癌细胞谱系的能力。癌症干细胞代表了一种适应能力很强的细胞群体。我们认为,癌症干细胞的高可进化性得益于它们在可塑性(增殖、对称分裂)和刚性(静止、不对称分裂,通常更具侵袭性)表型之间的反复转变,这些表型具有可塑性和刚性网络。因此,癌症干细胞多次逆转和重演癌症的发展。我们描述了潜在的网络模型,这些模型可以解释类似癌症干细胞的行为。最后,我们提出了新的策略,包括联合治疗和多靶点药物,以克服癌症干细胞靶向的尼采式困境:“杀不死我的,使我更强大”。