Department of Biochemistry and Molecular Genetics, University of Colorado School of Medicine, Aurora, CO 80045, United States.
Department of Biochemistry and Molecular Genetics, University of Colorado School of Medicine, Aurora, CO 80045, United States; Integrated Department of Immunology, University of Colorado School of Medicine, Aurora, CO 80045, United States; Department of Pediatrics, University of Colorado School of Medicine, Aurora, CO 80045, United States; Department of Medicine, Section of Hematology, University of Colorado School of Medicine, Aurora, CO 80045, United States.
Biochim Biophys Acta Rev Cancer. 2017 Apr;1867(2):84-94. doi: 10.1016/j.bbcan.2017.01.005. Epub 2017 Feb 4.
By the time the process of oncogenesis has produced an advanced cancer, tumor cells have undergone extensive evolution. The cellular phenotypes resulting from this evolution have been well studied, and include accelerated growth rates, apoptosis resistance, immortality, invasiveness, and immune evasion. Yet with all of our current knowledge of tumor biology, the details of early oncogenesis have been difficult to observe and understand. Where different oncogenic mutations may work together to enhance the survival of a tumor cell, in isolation they are often pro-apoptotic, pro-differentiative or pro-senescent, and therefore often, somewhat paradoxically, disadvantageous to a cell. It is also becoming clear that somatic mutations, including those in known oncogenic drivers, are common in tissues starting at a young age. These observations raise the question: how do we largely avoid cancer for most of our lives? Here we propose that evolutionary forces can help explain this paradox. As humans and other organisms age or experience external insults such as radiation or smoking, the structure and function of tissues progressively degrade, resulting in altered stem cell niche microenvironments. As tissue integrity declines, it becomes less capable of supporting and maintaining resident stem cells. These stem cells then find themselves in a microenvironment to which they are poorly adapted, providing a competitive advantage to those cells that can restore their functionality and fitness through mutations or epigenetic changes. The resulting oncogenic clonal expansions then increase the odds of further cancer progression. Understanding how the causes of cancer, such as aging or smoking, affect tissue microenvironments to control the impact of mutations on somatic cell fitness can help reconcile the discrepancy between marked mutation accumulation starting early in life and the somatic evolution that leads to cancer at advanced ages or following carcinogenic insults. This article is part of a Special Issue entitled: Evolutionary principles - heterogeneity in cancer?, edited by Dr. Robert A. Gatenby.
当致癌过程产生晚期癌症时,肿瘤细胞已经经历了广泛的进化。这种进化产生的细胞表型已经得到了很好的研究,包括加速的生长速度、凋亡抵抗、永生化、侵袭性和免疫逃逸。然而,尽管我们目前对肿瘤生物学有了很多了解,但早期致癌的细节仍然难以观察和理解。在不同的致癌突变可能共同作用以增强肿瘤细胞的生存能力的情况下,它们在孤立状态下通常是促凋亡、促分化或促衰老的,因此往往有些自相矛盾的是,对细胞不利。也越来越清楚的是,体细胞突变,包括已知致癌驱动因素中的突变,在年轻时的组织中就很常见。这些观察结果提出了一个问题:为什么我们在大部分生命中都能很好地避免癌症?在这里,我们提出进化力量可以帮助解释这个悖论。随着人类和其他生物的衰老或经历外部冲击,如辐射或吸烟,组织的结构和功能逐渐退化,导致干细胞生态位微环境发生改变。随着组织完整性的下降,它越来越难以支持和维持常驻干细胞。这些干细胞就会处于一个它们适应不良的微环境中,为那些能够通过突变或表观遗传变化恢复其功能和适应性的细胞提供竞争优势。由此产生的致癌克隆扩张增加了进一步癌症进展的可能性。了解癌症的原因(如衰老或吸烟)如何影响组织微环境,以控制突变对体细胞适应性的影响,可以帮助调和生命早期明显的突变积累与导致老年或致癌损伤后癌症发生的体细胞进化之间的差异。本文是题为“进化原则——癌症中的异质性?”的特刊的一部分,由罗伯特·A·盖滕比博士编辑。