Evidence map›Paper›PMID 31534127›Full record

ArticleCell death & disease2019

RNA-binding protein CELF6 is cell cycle regulated and controls cancer cell proliferation by stabilizing p21.

Gang Liu, Qianwen Zhang, Li Xia, Mengjuan Shi, Jin Cai, Haowei Zhang, Jia Li, Guanglan Lin, Weidong Xie, Yaou Zhang and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

21 citing papers in PubMed, 32 citations in OpenAlex.

  1. Review
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  5. CRL2BMC biology · 2025
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  16. MBNL2 Regulates DNA Damage Response via Stabilizing p21.International journal of molecular sciences · 2021
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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

11 authors at 3 institutions in 1 country.

Gang LiuState Key Laboratory of Chemical Oncogenomics, Tsinghua Shenzhen International Graduate School, Tsinghua University, 518055, Shenzhen, China.
Qianwen ZhangState Key Laboratory of Chemical Oncogenomics, Tsinghua Shenzhen International Graduate School, Tsinghua University, 518055, Shenzhen, China.
Li XiaState Key Laboratory of Chemical Oncogenomics, Tsinghua Shenzhen International Graduate School, Tsinghua University, 518055, Shenzhen, China.
Mengjuan ShiState Key Laboratory of Chemical Oncogenomics, Tsinghua Shenzhen International Graduate School, Tsinghua University, 518055, Shenzhen, China.
Jin CaiKey Lab in Healthy Science and Technology, Division of Life Science, Tsinghua Shenzhen International Graduate School, Tsinghua University, 518055, Shenzhen, China.
Haowei ZhangKey Lab in Healthy Science and Technology, Division of Life Science, Tsinghua Shenzhen International Graduate School, Tsinghua University, 518055, Shenzhen, China.
Jia LiKey Lab in Healthy Science and Technology, Division of Life Science, Tsinghua Shenzhen International Graduate School, Tsinghua University, 518055, Shenzhen, China.
Guanglan LinKey Lab in Healthy Science and Technology, Division of Life Science, Tsinghua Shenzhen International Graduate School, Tsinghua University, 518055, Shenzhen, China.
Weidong XieState Key Laboratory of Chemical Oncogenomics, Tsinghua Shenzhen International Graduate School, Tsinghua University, 518055, Shenzhen, China.
Yaou ZhangState Key Laboratory of Chemical Oncogenomics, Tsinghua Shenzhen International Graduate School, Tsinghua University, 518055, Shenzhen, China.
Naihan XuState Key Laboratory of Chemical Oncogenomics, Tsinghua Shenzhen International Graduate School, Tsinghua University, 518055, Shenzhen, China. xu.naihan@sz.tsinghua.edu.cn.
Tsinghua–Berkeley Shenzhen Institute · CNTsinghua University · CNUniversity Town of Shenzhen · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CELF6, a member of the CELF family of RNA-binding proteins, regulates muscle-specific alternative splicing and contributes to the pathogenesis of myotonic dystrophy (DM), however the role of CELF6 in cancer cell proliferation is less appreciated. Here, we show that the expression of CELF6 is cell cycle regulated. The cell cycle-dependent expression of CELF6 is mediated through the ubiquitin-proteasome pathway, SCF-β-TrCP recognizes a nonphospho motif in CELF6 and regulates its proteasomal degradation. Overexpression or depletion of CELF6 modulates p21 gene expression. CELF6 binds to the 3'UTR of p21 transcript and increases its mRNA stability. Depletion of CELF6 promotes cell cycle progression, cell proliferation and colony formation whereas overexpression of CELF6 induces G1 phase arrest. The effect of CELF6 on cell proliferation is p53 and/or p21 dependent. Collectively, these data demonstrate that CELF6 might be a potential tumor suppressor, CELF6 regulates cell proliferation and cell cycle progression via modulating p21 stability.

Indexed as

CELF ProteinsCell CycleCell ProliferationCyclin-Dependent Kinase Inhibitor p21Gene Knockout TechniquesHCT116 CellsHEK293 CellsHumansProteasome Endopeptidase ComplexProtein StabilityRNA, MessengerSignal TransductionSKP Cullin F-Box Protein LigasesTumor Suppressor Protein p53UbiquitinCDKN1A protein, humanCELF6 protein, humanCELF ProteinsCyclin-Dependent Kinase Inhibitor p21Proteasome Endopeptidase ComplexRNA, MessengerSKP Cullin F-Box Protein LigasesTP53 protein, humanTumor Suppressor Protein p53Ubiquitin

Identifiers

PMID31534127
PMCPMC6751195
OpenAlexW2974848401

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.