Alberghina Lilia, Chiaradonna Ferdinando, Vanoni Marco
Department of Biotechnology and Biosciences, Universiy of Milano-Bicocca, Piazza della Scienza 2, 20126 Milano, Italy.
Chembiochem. 2004 Oct 4;5(10):1322-33. doi: 10.1002/cbic.200400170.
Proliferative disorders are a major challenge for human health. The understanding of the organization of cell-cycle events is of the utmost importance to devise effective therapeutic strategies for cancer. The awareness that cells and organisms are complex, modular, hierarchical systems and the availability of genome-wide gene expression and protein analyses, should make it feasible to elucidate human diseases in terms of dysfunctions of molecular systems. Here we review evidence in support of a systems model of the cell cycle, in which two sequential growth-sensitive thresholds control entry into S-phase. The putative molecular determinants that set the threshold for entry into S-phase are consistently altered in cancer cells. Such a framework could be useful in guiding both experimental investigation and data analysis by allowing wiring to other relevant cell modules thereby highlighting the differential responses, or lack of response of cancer cells to intra- and extracellular factors. Pharmacological approaches that take advantage of transformation-induced fragility to glucose shortage are discussed. Extension of this hierarchical, modular approach to tumors as a whole holds promise for the development of effective drug discovery approaches and more efficient therapeutic protocols.
增殖性疾病是人类健康面临的重大挑战。了解细胞周期事件的组织对于设计有效的癌症治疗策略至关重要。认识到细胞和生物体是复杂的、模块化的、分层的系统,以及全基因组基因表达和蛋白质分析的可得性,应该使得从分子系统功能障碍的角度阐明人类疾病变得可行。在这里,我们综述支持细胞周期系统模型的证据,其中两个连续的生长敏感阈值控制进入S期。设定进入S期阈值的假定分子决定因素在癌细胞中持续发生改变。这样一个框架可能有助于指导实验研究和数据分析,通过允许与其他相关细胞模块建立联系,从而突出癌细胞对细胞内和细胞外因素的不同反应或无反应。讨论了利用转化诱导的对葡萄糖缺乏的脆弱性的药理学方法。将这种分层的、模块化的方法扩展到整个肿瘤有望开发出有效的药物发现方法和更有效的治疗方案。