White Donald E, Rayment Jonathan H, Muller William J
Molecular Oncology Group and Department of Biochemistry, McGill University, Montreal, Quebec, Canada.
Cell Cycle. 2006 Aug;5(16):1756-9. doi: 10.4161/cc.5.16.2993. Epub 2006 Aug 15.
The dissemination of tumor cells prior to the surgical resection of early stage tumors poses a serious risk to the disease free survival of cancer patients. This risk arises from the latent capacity of these cells to form solid metastatic lesions after a prolonged period of dormancy, exacerbated by the fact that these cells are often refractory to adjuvant chemotherapeutic protocols. Ensuring the long term survival of cancer patients therefore necessitates an understanding of the mechanisms of tumor cell dormancy and the accompanying drug resistance. Experiments designed to compare the biological behavior of metastatic versus nonmetastatic variants of tumor cells provide evidence that there exists a phenomenon of single-cell dormancy which may depend on a reciprocal dialogue between the tumor cell and the tissue microenvironment. Through a combination of 3-dimensional cell culture technique and in vivo models investigators are now beginning to elucidate the molecular mechanisms underlying this phenomenon. Here we review the results of a series of experiments describing the role of cell adhesion events in dictating tumor cell behavior, including the balance between proliferation and dormancy, and the acquisition of drug resistance.
在早期肿瘤手术切除之前,肿瘤细胞的播散对癌症患者的无病生存期构成严重风险。这种风险源于这些细胞在长期休眠后形成实体转移病灶的潜在能力,而这些细胞往往对辅助化疗方案具有抗性,这一事实加剧了这种风险。因此,要确保癌症患者的长期生存,就必须了解肿瘤细胞休眠机制及伴随的耐药性。旨在比较肿瘤细胞转移变体与非转移变体生物学行为的实验表明,存在一种单细胞休眠现象,这可能取决于肿瘤细胞与组织微环境之间的相互对话。通过三维细胞培养技术和体内模型相结合,研究人员现在开始阐明这一现象背后的分子机制。在此,我们回顾一系列实验的结果,这些实验描述了细胞黏附事件在决定肿瘤细胞行为中的作用,包括增殖与休眠之间的平衡以及耐药性的获得。