Evidence map›Paper›PMID 30535125›Full record

ArticleNucleic acids research2019

FOXO1 degradation via G9a-mediated methylation promotes cell proliferation in colon cancer.

Yun-Cheol Chae, Ji-Young Kim, Jin Woo Park, Kee-Beom Kim, Hyein Oh, Kyung-Hwa Lee, Sang-Beom Seo

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 74 papers.

0numbers the graph read from it
0cells of the map it votes in
74citing papers in PubMed
3.5field-weighted citation impact, top 6% 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

74 citing papers in PubMed, 132 citations in OpenAlex.

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  17. EHMT2-mediated transcriptional reprogramming drives neuroendocrine transformation in non-small cell lung cancer.Proceedings of the National Academy of Sciences of the United States of America · 2024
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14 more citing papers are in PubMed but not listed here.

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

7 authors at 2 institutions in 1 country.

Yun-Cheol ChaeDepartment of Life Science, College of Natural Sciences, Chung-Ang University, Seoul 156-756, South Korea.
Ji-Young KimDepartment of Life Science, College of Natural Sciences, Chung-Ang University, Seoul 156-756, South Korea.
Jin Woo ParkDepartment of Life Science, College of Natural Sciences, Chung-Ang University, Seoul 156-756, South Korea.
Kee-Beom KimDepartment of Life Science, College of Natural Sciences, Chung-Ang University, Seoul 156-756, South Korea.
Hyein OhDepartment of Life Science, College of Natural Sciences, Chung-Ang University, Seoul 156-756, South Korea.
Kyung-Hwa LeeDepartment of Pathology, Chonnam National University Hwasun Hospital and Medical School, Hwasun, Jeollanam-do, South Korea.
Sang-Beom SeoDepartment of Life Science, College of Natural Sciences, Chung-Ang University, Seoul 156-756, South Korea.
Chung-Ang University · KRChonnam National University Hwasun Hospital · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Posttranslational modifications of the Forkhead family transcription factor, FOXO1, have been known to have important regulatory implications in its diverse activities. Several types of modifications of FOXO1, including acetylation, phosphorylation, and ubiquitination, have been reported. However, lysine methylation of FOXO1 has not yet been identified. Here, we reported that FOXO1 is methylated by G9a at K273 residue in vitro and in vivo. Methylation of FOXO1 by G9a increased interaction between FOXO1 and a specific E3 ligase, SKP2, and decreased FOXO1 protein stability. In addition, G9a expression was increased by insulin and resulted in insulin-mediated FOXO1 degradation by K273 methylation. Tissue array analysis indicated that G9a was overexpressed and FOXO1 levels decreased in human colon cancer. Cell proliferation assays revealed that G9a-mediated FOXO1 methylation increased colon cancer cell proliferation. Fluorescence-activated cell sorting (FACS) analysis indicated that apoptosis rates were higher in the presence of FOXO1 than in FOXO1 knock-out cells. Furthermore, we found that G9a protein levels were elevated and FOXO1 protein levels were decreased in human colon cancer patients tissue samples. Here, we report that G9a specific inhibitor, BIX-01294, can regulate cell proliferation and apoptosis by inhibiting G9a-mediated FOXO1 methylation.

Indexed as

ApoptosisAzepinesCell ProliferationColonic NeoplasmsCRISPR-Cas SystemsDNA MethylationFemaleFlow CytometryForkhead Box Protein O1Gene Expression Regulation, NeoplasticGene Knockout TechniquesHCT116 CellsHistocompatibility AntigensHistone-Lysine N-MethyltransferaseHumansMaleAzepinesBIX 01294EHMT2 protein, humanForkhead Box Protein O1FOXO1 protein, humanHistocompatibility AntigensHistone-Lysine N-MethyltransferaseQuinazolinesSKP2 protein, humanS-Phase Kinase-Associated Proteins

Identifiers

PMID30535125
PMCPMC6393239
OpenAlexW2905324652

What Socratic holds

Textmetadata
LicenceCC BY-NC
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 Socratic graph.