Garcia S B, Park H S, Novelli M, Wright N A
Histopathology Unit, Imperial Cancer Research Fund, London, U.K.
J Pathol. 1999 Jan;187(1):61-81. doi: 10.1002/(SICI)1096-9896(199901)187:1<61::AID-PATH247>3.0.CO;2-I.
There has been considerable debate about the origin of human tumours, whether they arise from a single cell and are clonal populations or whether there needs to be some sort of co-operativity between cells for the neoplastic process to begin. Current theories subscribe to the clonal view, where a series of mutations in one cell begins a process of selection and clonal evolution leading to the development of the malignant phenotype. This review approaches this problem by asking how mutated clones, once established, spread through tissues before becoming overtly invasive. While there is substantial evidence in favour of independent origins of each tumour from a unique mutated clone, there are instances where such clones expand and remain cohesive, often involving a large area of tissue. The main example is the movement of mutated clonal crypts through the colorectal epithelium, by the process of crypt fission. In passing, the clonal architecture of early, pre-invasive lesions is examined, often with some surprising results.
关于人类肿瘤的起源存在相当多的争论,即它们是源自单个细胞并形成克隆群体,还是在肿瘤形成过程开始时细胞之间需要某种协同作用。目前的理论支持克隆观点,即一个细胞中的一系列突变启动了选择和克隆进化过程,导致恶性表型的发展。本综述通过询问突变克隆一旦形成后如何在组织中扩散直至变得明显侵袭性来探讨这个问题。虽然有大量证据支持每个肿瘤独立起源于独特的突变克隆,但也有一些情况是这样的克隆会扩张并保持聚集性,通常涉及大面积组织。主要例子是突变的克隆性隐窝通过隐窝裂变过程在结直肠上皮中移动。顺便说一下,还研究了早期非侵袭性病变的克隆结构,结果往往有些令人惊讶。