Evidence map›Paper›PMID 33468253›Full record

ArticleCell & bioscience2021

Neural stemness contributes to cell tumorigenicity.

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

Abstract read
In one paragraph

Article in Cell & bioscience, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

24 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Liyang Xu *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.
Min Zhang *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.
Lihua ShiMOE 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.
Xiaoli YangMOE 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.
Lu ChenMOE 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.
Ning CaoMOE 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.
Anhua LeiMOE 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.
Ying CaoMOE 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. caoying@nju.edu.cn.ORCID http://orcid.org/0000-0001-8286-9591

Funding

National Natural Science Foundation of China 31671499
6 · The paper itself

Abstract

backgroundPrevious 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.

resultsWe 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.

conclusionsWe 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.

Indexed as

Differentiation potentialEvo-devoNeural ground stateNeural stemnessNeural stem/progenitor cellTumorigenesisTumorigenicityTumor-initiating cell

Identifiers

PMID33468253
PMCPMC7814647

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.