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The Convergent Cancer Evolution toward a Single Cellular Destination

机译:趋向单一细胞目的地的融合癌症演变

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The essence of Darwin's theory is that evolution is driven by purposeless mutations that are subsequently selected by natural environments, so there is often no predefined destination in organismal evolution. Using gene expressions of 107 cell types, we built a functional space of human cells to trace the evolutionary trajectory of 18 types of solid tumor cancers. We detected a dominant evolving trend toward the functional status of embryonic stem cells (ESC) for approximately 3,000 tumors growing in distinct tissue environments. This pattern remained the same after excluding known cancer/ESC signature genes (similar to 3,000 genes) or excluding all oncogenic gene sets (similar to 12,000 genes) annotated in MSigDB, suggesting a convergent evolution of the overall functional status in cancers. In support of this, the functional distance to ESC served as a common prognostic indicator for cancers of various types, with shorter distance corresponding to poor prognosis, which was true even when randomly selected gene sets were considered. Thus, regardless of the external environments, cancer evolution is a directional process toward a defined cellular destination, a finding reconciling development and evolution, the two seemingly incompatible philosophies both adopted by the cancer research community, and also raising new questions to evolutionary biology.
机译:达尔文理论的本质是进化是由无目的的突变驱动的,随后自然环境选择了这些突变,因此有机体进化中通常没有预先确定的目的地。使用107种细胞类型的基因表达,我们建立了人类细胞的功能空间,以追踪18种实体瘤癌症的进化轨迹。我们检测到在不同组织环境中生长的大约3,000个肿瘤的胚胎干细胞(ESC)功能状态的主要进化趋势。在排除已知的癌症/ ESC签名基因(类似于3,000个基因)或排除MSigDB中注释的所有致癌基因集(类似于12,000个基因)之后,这种模式保持不变,这表明癌症总体功能状态的趋同演变。支持这一点的是,到ESC的功能距离是各种类型癌症的常见预后指标,距离越短,预后就越差,即使考虑随机选择的基因集,也是如此。因此,无论外部环境如何,癌症进化都是朝着确定的细胞目的地发展的方向性过程,这一发现使发展与进化协调一致,这两个看似不相容的哲学都被癌症研究界所采用,并且对进化生物学提出了新的问题。

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