Compagni A, Christofori G
Research Institute of Molecular Pathology, Vienna, Austria.
Br J Cancer. 2000 Jul;83(1):1-5. doi: 10.1054/bjoc.2000.1309.
Tumour development is a multi-step process during which genetic and epigenetic events determine the transition from a normal to a malignant cellular state. In the past decade, extensive effort has been made not only to define the molecular mechanisms underlying progression to malignancy but also to predict the development of the disease and to identify possible molecular targets for therapy. Common to most tumours, several regulatory circuits are altered during multistage tumour progression, most importantly, the control of proliferation, the balance between cell survival and programmed cell death (apoptosis), the communication with neighbouring cells and the extracellular matrix, the induction of tumour neovascularization (angiogenesis) and, finally, tumour cell migration, invasion and metastatic dissemination. De-regulation of each of these processes represents a rate-limiting step for tumour development and, hence, has to be achieved by tumour cells in a highly selective manner during tumour progression. In this review we summarize recent advances in cancer research that have provided new insights in the molecular mechanisms underlying the transition between one tumour stage and the next and into their concerted action during tumour progression. Cultured human tumour cell lines as well as transgenic and knock-out mouse models of tumorigenesis have been instrumental in these experimental approaches.
肿瘤发展是一个多步骤过程,在此过程中,基因和表观遗传事件决定了从正常细胞状态向恶性细胞状态的转变。在过去十年中,人们不仅付出了巨大努力来确定恶性进展的分子机制,还致力于预测疾病的发展并确定可能的治疗分子靶点。大多数肿瘤的共同特征是,在多阶段肿瘤进展过程中,几个调节回路会发生改变,最重要的是增殖控制、细胞存活与程序性细胞死亡(凋亡)之间的平衡、与邻近细胞和细胞外基质的通讯、肿瘤新生血管形成(血管生成)的诱导,以及最终肿瘤细胞的迁移、侵袭和转移扩散。这些过程中每一个的失调都是肿瘤发展的限速步骤,因此,肿瘤细胞在肿瘤进展过程中必须以高度选择性的方式实现这些失调。在本综述中,我们总结了癌症研究的最新进展,这些进展为一个肿瘤阶段与下一个阶段之间转变的分子机制以及它们在肿瘤进展过程中的协同作用提供了新的见解。培养的人类肿瘤细胞系以及肿瘤发生的转基因和基因敲除小鼠模型在这些实验方法中发挥了重要作用。