Evidence map›Paper›PMID 33791755›Full record

ArticleCerebral cortex (New York, N.Y. : 1991)2021

Transcriptome Regulation by Oncogenic ALK Pathway in Mammalian Cortical Development Revealed by Single-Cell RNA Sequencing.

Rui Mao, Xiaoyun Zhang, Youyong Kong, Shanshan Wu, Hai-Qin Huo, Yue Kong, Zhen Wang, Yan Liu, Zhengping Jia, Zikai Zhou

Open access · greenAbstract read
In one paragraph

Article in Cerebral cortex (New York, N.Y. : 1991), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
0.2field-weighted citation impact, top 48% of its field
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

4 citing papers in PubMed, 1 synthesis or guideline pooled it, 3 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Review
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

10 authors at 6 institutions in 2 countries.

Rui MaoShanghai Key Laboratory of Psychotic Disorders, Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, 200030 China.
Xiaoyun ZhangShanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 201203 China.
Youyong KongSchool of Computer Science and Engineering, Southeast University, Nanjing, 210096 China.
Shanshan WuState Key Laboratory of Reproductive Medicine, Nanjing Medical University, Nanjing, 211166 China.
Hai-Qin HuoState Key Laboratory of Reproductive Medicine, Nanjing Medical University, Nanjing, 211166 China.
Yue KongSchool of Life Science and Technology, Southeast University, Nanjing, 210096 China.
Zhen WangShanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 201203 China.
Yan LiuState Key Laboratory of Reproductive Medicine, Nanjing Medical University, Nanjing, 211166 China.
Zhengping JiaNeurosciences & Mental Health, The Hospital for Sick Children, Toronto, Ontario, M5G 1X8 Canada.
Zikai ZhouShanghai Key Laboratory of Psychotic Disorders, Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, 200030 China.
Nanjing Medical University · CNShanghai Institute of Materia Medica · CNSoutheast University · CNNantong University · CNShanghai Mental Health Center · CNUniversity of Toronto · CA

Funding

Canadian Natural Science and Engineering Research Council RGPIN341498CIHR MOP119421Jiangsu Outstanding Young Investigator Program BK20160044National Key Research and Development Program of China 2016YFC1306703National Natural Science Foundation of China 81971022Program of Shanghai Academic Research Leader 19XD1423300Science and Technology Commission of Shanghai Municipality 201409002600Shanghai Mental Health Center-Clinical Research Center CRC2019ZD01Shanghai Municipal Education Commission-Gaofeng Clinical Medicine 20191835
6 · The paper itself

Abstract

Precise regulation of embryonic neurodevelopment is crucial for proper structural organization and functioning of the adult brain. The key molecular machinery orchestrating this process remains unclear. Anaplastic lymphoma kinase (ALK) is an oncogenic receptor-type protein tyrosine kinase that is specifically and transiently expressed in developing nervous system. However, its role in the mammalian brain development is unknown. We found that transient embryonic ALK inactivation caused long-lasting abnormalities in the adult mouse brain, including impaired neuronal connectivity and cognition, along with delayed neuronal migration and decreased neuronal proliferation during neurodevelopment. scRNA-seq on human cerebral organoids revealed a delayed transition of cell-type composition. Molecular characterization identified a group of differentially expressed genes (DEGs) that were temporally regulated by ALK at distinct developmental stages. In addition to oncogenes, many DEGs found by scRNA-seq are associated with neurological or neuropsychiatric disorders. Our study demonstrates a pivotal role of oncogenic ALK pathway in neurodevelopment and characterized cell-type-specific transcriptome regulated by ALK for better understanding mammalian cortical development.

Indexed as

TranscriptomeAnaplastic Lymphoma KinaseAnimalsCerebral CortexFemaleGene Expression Regulation, DevelopmentalHumansMagnetic Resonance ImagingMiceNervous System DiseasesNeural Stem CellsNeurogenesisOncogenesPregnancyRNA-SeqSignal TransductionAlk protein, mouseAnaplastic Lymphoma Kinaseanaplastic lymphoma kinasecerebral organoidneural progenitor cellneurodevelopmentsingle-cell RNA sequencing

Identifiers

PMID33791755
PMCPMC8258437
OpenAlexW3144219494

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.