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神经干性有助于细胞的致瘤性。

Neural stemness contributes to cell tumorigenicity.

作者信息

Xu Liyang, Zhang Min, Shi Lihua, Yang Xiaoli, Chen Lu, Cao Ning, Lei Anhua, Cao Ying

机构信息

MOE Key Laboratory of Model Animals for Disease Study, and Model Animal Research Center of the Medical School, Nanjing University, 12 Xuefu Road, Pukou High-Tech Zone, Nanjing, 210061, China.

出版信息

Cell Biosci. 2021 Jan 19;11(1):21. doi: 10.1186/s13578-021-00531-6.

Abstract

BACKGROUND

Previous studies demonstrated the dependence of cancer on nerve. Recently, a growing number of studies reveal that cancer cells share the property and regulatory network with neural stem/progenitor cells. However, relationship between the property of neural stemness and cell tumorigenicity is unknown.

RESULTS

We show that neural stem/progenitor cells, but not non-neural embryonic or somatic stem/progenitor cell types, exhibit tumorigenicity and the potential for differentiation into tissue types of all germ layers when they are placed in non-native environment by transplantation into immunodeficient nude mice. Likewise, cancer cells capable of tumor initiation have the property of neural stemness because of their abilities in neurosphere formation in neural stem cell-specific serum-free medium and in differentiation potential, in addition to their neuronal differentiation potential that was characterized previously. Moreover, loss of a pro-differentiation factor in myoblasts, which have no tumorigenicity, lead to the loss of myoblast identity, and gain of the property of neural stemness, tumorigenicity and potential for re-differentiation. By contrast, loss of neural stemness via differentiation results in the loss of tumorigenicity. These suggest that the property of neural stemness contributes to cell tumorigenicity, and tumor phenotypic heterogeneity might be an effect of differentiation potential of neural stemness. Bioinformatic analysis reveals that neural genes in general are correlated with embryonic development and cancer, in addition to their role in neural development; whereas non-neural genes are not. Most of neural specific genes emerged in typical species representing transition from unicellularity to multicellularity during evolution. Genes in Monosiga brevicollis, a unicellular species that is a closest known relative of metazoans, are biased toward neural cells.

CONCLUSIONS

We suggest that the property of neural stemness is the source of cell tumorigenicity. This is due to that neural biased unicellular state is the ground state for multicellularity and hence cell type diversification or differentiation during evolution, and tumorigenesis is a process of restoration of neural ground state in somatic cells along a default route that is pre-determined by an evolutionary advantage of neural state.

摘要

背景

先前的研究表明癌症对神经存在依赖性。最近,越来越多的研究揭示癌细胞与神经干/祖细胞具有共同的特性和调控网络。然而,神经干性特性与细胞致瘤性之间的关系尚不清楚。

结果

我们发现,当通过移植到免疫缺陷裸鼠体内而置于非天然环境中时,神经干/祖细胞而非非神经胚胎或体细胞干/祖细胞类型表现出致瘤性以及分化为所有胚层组织类型的潜力。同样,具有肿瘤起始能力的癌细胞具有神经干性特性,这不仅体现在其先前已被表征的神经元分化潜力上,还体现在它们在神经干细胞特异性无血清培养基中形成神经球的能力以及分化潜力上。此外,在没有致瘤性的成肌细胞中,一个促分化因子的缺失导致成肌细胞特性丧失,并获得神经干性、致瘤性和再分化潜力。相反,通过分化导致神经干性丧失会致使致瘤性丧失。这些表明神经干性特性有助于细胞致瘤性,并且肿瘤表型异质性可能是神经干性分化潜力的一种效应。生物信息学分析表明,一般而言,神经基因除了在神经发育中的作用外,还与胚胎发育和癌症相关;而非神经基因则不然。大多数神经特异性基因出现在进化过程中代表从单细胞向多细胞转变的典型物种中。在与后生动物关系最近的已知单细胞物种短柄单歧藻中,基因偏向于神经细胞。

结论

我们认为神经干性特性是细胞致瘤性的来源。这是因为神经偏向的单细胞状态是多细胞性的基态,因此也是进化过程中细胞类型多样化或分化的基态,而肿瘤发生是体细胞沿着由神经状态的进化优势预先确定的默认途径恢复神经基态的过程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c620/7814647/31621b8eb182/13578_2021_531_Fig1_HTML.jpg

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