Planetary Science Institute, Research School of Astronomy and Astrophysics & Research School of Earth Sciences, The Australian National University, Canberra, ACT, Australia.
Mt Stromlo Observatory, Canberra, ACT, Australia.
Bioessays. 2021 Jul;43(7):e2000305. doi: 10.1002/bies.202000305. Epub 2021 May 13.
It has long been recognized that cancer onset and progression represent a type of reversion to an ancestral quasi-unicellular phenotype. This general concept has been refined into the atavistic model of cancer that attempts to provide a quantitative analysis and testable predictions based on genomic data. Over the past decade, support for the multicellular-to-unicellular reversion predicted by the atavism model has come from phylostratigraphy. Here, we propose that cancer onset and progression involve more than a one-off multicellular-to-unicellular reversion, and are better described as a series of reversionary transitions. We make new predictions based on the chronology of the unicellular-eukaryote-to-multicellular-eukaryote transition. We also make new predictions based on three other evolutionary transitions that occurred in our lineage: eukaryogenesis, oxidative phosphorylation and the transition to adaptive immunity. We propose several modifications to current phylostratigraphy to improve age resolution to test these predictions. Also see the video abstract here: https://youtu.be/3unEu5JYJrQ.
长期以来,人们一直认识到癌症的发生和进展代表了一种向祖先拟单细胞表型的逆转。这个一般概念已经被细化为癌症的返祖模型,该模型试图基于基因组数据进行定量分析和可测试的预测。在过去的十年中,基于返祖模型预测的多细胞到单细胞的逆转得到了系统发生学的支持。在这里,我们提出癌症的发生和进展不仅仅涉及一次性的多细胞到单细胞的逆转,而是可以更好地描述为一系列的返祖性转变。我们基于单细胞真核生物到多细胞真核生物的过渡的时间顺序提出了新的预测。我们还基于我们谱系中发生的另外三个进化转变提出了新的预测:真核生物起源、氧化磷酸化和适应性免疫的转变。我们建议对当前的系统发生学进行一些修改,以提高年龄分辨率来测试这些预测。也可在此处观看视频摘要:https://youtu.be/3unEu5JYJrQ。