Lady Davis Institute for Medical Research, Jewish General Hospital, Montreal, Quebec, Canada; Segal Cancer Center, Jewish General Hospital, Montreal, Quebec, Canada; Department of Human Genetics, McGill University, Montreal, Quebec, Canada; Department of Nursing, McGill University, Montreal, Quebec, Canada.
Lady Davis Institute for Medical Research, Jewish General Hospital, Montreal, Quebec, Canada; Segal Cancer Center, Jewish General Hospital, Montreal, Quebec, Canada; Department of Medicine, McGill University, Montreal, Quebec, Canada.
Trends Cancer. 2021 May;7(5):400-409. doi: 10.1016/j.trecan.2020.10.013. Epub 2020 Nov 23.
Tumor genetic heterogeneity, in which individual tumors contain both multiple variant cancer-associated and normal genes, has been widely reported, although its significance has yet to be fully understood. We propose a genetic heterogeneity-based selection-centric hypothesis in which genetic heterogeneity, caused by the temporary reduction of DNA repair efficiency, occurs very early in human development, resulting in a small minority of cells in normal tissues acquiring cancer-associated genes that remain dormant. Cancer develops when precancer cells are selected for by altered tissue microenvironments; similar scenarios occur with development of metastases and therapeutic resistance in established cancer. This suggests that a normal cell selection treatment approach based on preferentially selecting normal cells within tumors may be effective in treating cancer.
肿瘤遗传异质性,即个别肿瘤同时含有多种变异的癌症相关基因和正常基因,已被广泛报道,尽管其意义尚未被完全理解。我们提出了一个基于遗传异质性的选择中心假说,即在人类发育的早期,由于 DNA 修复效率的暂时降低,导致正常组织中的一小部分细胞获得了处于休眠状态的癌症相关基因,从而导致遗传异质性的发生。当癌前细胞被改变的组织微环境选择时,癌症就会发生;在已建立的癌症中转移和治疗耐药性的发展也会出现类似的情况。这表明,基于优先选择肿瘤内正常细胞的正常细胞选择治疗方法可能对治疗癌症有效。