Evidence map›Paper›PMID 32229723›Full record

ArticleJCI insight2020

CIC is a critical regulator of neuronal differentiation.

Inah Hwang, Heng Pan, Jun Yao, Olivier Elemento, Hongwu Zheng, Jihye Paik

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2020. 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
2.2field-weighted citation impact, top 11% 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

24 citing papers in PubMed, 45 citations in OpenAlex.

  1. Trial
  2. Article
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  7. Capicua Refines Mossy Fiber-CA3 Axon Targeting in the Late Postnatal Hippocampus.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  8. Review
  9. Article
  10. Article
  11. Molecular and therapeutic advancements in Capicua (Frontiers in cell and developmental biology · 2024
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
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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

6 authors at 3 institutions in 3 countries.

Inah HwangDepartment of Pathology and Laboratory Medicine.
Heng PanMeyer Cancer Center, and.
Jun YaoDepartment of Molecular and Cellular Oncology, University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Olivier ElementoMeyer Cancer Center, and.
Hongwu ZhengDepartment of Pathology and Laboratory Medicine.
Jihye PaikDepartment of Pathology and Laboratory Medicine.
Meyer (China) · CNCornell University · USThe University of Texas MD Anderson Cancer Center · US

Funding

The Mechanisms Underlying How Oxidative Stress Influences Neural Stem Cell FateR01AG048284 · NIA · WEILL MEDICAL COLL OF CORNELL UNIV · PI PAIK, JIHYE · 2014 to 2018
$1.7M
Mechanisms underlying integrated stress response induced inflammationR56AG048284 · NIA · WEILL MEDICAL COLL OF CORNELL UNIV · PI PAIK, JIHYE · 2019 to 2019
$424k
NIA NIH HHS R01 AG048284NIA NIH HHS R56 AG048284
6 · The paper itself

Abstract

Capicua (CIC), a member of the high mobility group-box (HMG-box) superfamily of transcriptional repressors, is frequently mutated in human oligodendrogliomas. However, its functions in brain development and tumorigenesis remain poorly understood. Here, we report that brain-specific deletion of Cic compromises developmental transition of neuroblasts to immature neurons in mouse hippocampus and compromises normal neuronal differentiation. Combined gene expression and ChIP-seq analyses identified VGF as an important CIC-repressed transcriptional surrogate involved in neuronal lineage regulation. Aberrant VGF expression promotes neural progenitor cell proliferation by suppressing their differentiation. Mechanistically, we demonstrated that CIC represses VGF expression by tethering SIN3-HDAC to form a transcriptional corepressor complex. Mass spectrometry analysis of CIC-interacting proteins further identified the BRG1-containing mSWI/SNF complex whose function is necessary for transcriptional repression by CIC. Together, this study uncovers a potentially novel regulatory pathway of CIC-dependent neuronal differentiation and may implicate these molecular mechanisms in CIC-dependent brain tumorigenesis.

Indexed as

AnimalsCarcinogenesisCell DifferentiationCell ProliferationCells, CulturedGene Expression Regulation, DevelopmentalHippocampusMiceMice, Inbred C57BLMice, KnockoutNeural Stem CellsNeuronsOligodendrogliomaRepressor ProteinsCic protein, mouseRepressor ProteinsBrain cancerNeuronal stem cellsOncologyStem cellsTranscription

Identifiers

PMID32229723
PMCPMC7253013
OpenAlexW3013092454

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.