Evidence map›Paper›PMID 34972816›Full record

ArticleThe ISME journal2022

Human gut-microbiome-derived propionate coordinates proteasomal degradation via HECTD2 upregulation to target EHMT2 in colorectal cancer.

Tae Young Ryu, Kwangho Kim, Tae-Su Han, Mi-Ok Lee, Jinkwon Lee, Jinhyeon Choi, Kwang Bo Jung, Eun-Jeong Jeong, Da Mi An, Cho-Rok Jung and 12 more

Open access · hybridAbstract read
In one paragraph

Article in The ISME journal, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 85 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
85citing papers in PubMed, 1 pooled it
9.9field-weighted citation impact, top 1% 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

85 citing papers in PubMed, 1 synthesis or guideline pooled it, 126 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Propionate promotes CD8Journal for immunotherapy of cancer · 2026
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25 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

22 authors at 5 institutions in 4 countries.

Tae Young Ryu *Korea Research Institute of Bioscience and Biotechnology, Daejeon, 34141, Republic of Korea.
Kwangho Kim *Korea Research Institute of Bioscience and Biotechnology, Daejeon, 34141, Republic of Korea.
Tae-Su Han *Korea Research Institute of Bioscience and Biotechnology, Daejeon, 34141, Republic of Korea.
Mi-Ok LeeKorea Research Institute of Bioscience and Biotechnology, Daejeon, 34141, Republic of Korea.
Jinkwon LeeKorea Research Institute of Bioscience and Biotechnology, Daejeon, 34141, Republic of Korea.
Jinhyeon ChoiKorea Research Institute of Bioscience and Biotechnology, Daejeon, 34141, Republic of Korea.
Kwang Bo JungKorea Research Institute of Bioscience and Biotechnology, Daejeon, 34141, Republic of Korea.
Eun-Jeong JeongKorea Research Institute of Bioscience and Biotechnology, Daejeon, 34141, Republic of Korea.
Da Mi AnKorea Research Institute of Bioscience and Biotechnology, Daejeon, 34141, Republic of Korea.
Cho-Rok JungKorea Research Institute of Bioscience and Biotechnology, Daejeon, 34141, Republic of Korea.
Jung Hwa LimKorea Research Institute of Bioscience and Biotechnology, Daejeon, 34141, Republic of Korea.
Jaeeun JungKorea Research Institute of Bioscience and Biotechnology, Daejeon, 34141, Republic of Korea.
Kunhyang ParkKorea Research Institute of Bioscience and Biotechnology, Daejeon, 34141, Republic of Korea.
Moo-Seung LeeKorea Research Institute of Bioscience and Biotechnology, Daejeon, 34141, Republic of Korea.
Mi-Young KimDepartment of Biological Sciences, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, 34141, Republic of Korea.
Soo Jin OhAsan Institute for Life Sciences, Asan Medical Center and Department of Convergence Medicine, College of Medicine, University of Ulsan, Seoul, 05505, Republic of Korea.
Keun HurDepartment of Biochemistry and Cell biology, School of Medicine, Kyungpook National University, Daegu, 41944, Republic of Korea.
Ryuji HamamotoDivision of Molecular Modification and Cancer Biology, National Cancer Center, Tokyo, 104-0045, Japan.
Doo-Sang ParkKorea Research Institute of Bioscience and Biotechnology, Daejeon, 34141, Republic of Korea. dspark@kribb.re.kr.ORCID http://orcid.org/0000-0003-4528-6789
Dae-Soo KimKorea Research Institute of Bioscience and Biotechnology, Daejeon, 34141, Republic of Korea. kds2465@kribb.re.kr.ORCID http://orcid.org/0000-0002-4999-1613
Mi-Young SonKorea Research Institute of Bioscience and Biotechnology, Daejeon, 34141, Republic of Korea. myson@kribb.re.kr.ORCID http://orcid.org/0000-0001-7590-8812
Hyun-Soo ChoKorea Research Institute of Bioscience and Biotechnology, Daejeon, 34141, Republic of Korea. chohs@kribb.re.kr.ORCID http://orcid.org/0000-0002-8242-9390
Korea Research Institute of Bioscience and Biotechnology · KRKorea Advanced Institute of Science and Technology · KRAsan Medical Center · KRKyungpook National University · KRNational Cancer Centre Japan · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The human microbiome plays an essential role in the human immune system, food digestion, and protection from harmful bacteria by colonizing the human intestine. Recently, although the human microbiome affects colorectal cancer (CRC) treatment, the mode of action between the microbiome and CRC remains unclear. This study showed that propionate suppressed CRC growth by promoting the proteasomal degradation of euchromatic histone-lysine N-methyltransferase 2 (EHMT2) through HECT domain E3 ubiquitin protein ligase 2 (HECTD2) upregulation. In addition, EHMT2 downregulation reduced the H3K9me2 level on the promoter region of tumor necrosis factor α-induced protein 1 (TNFAIP1) as a novel direct target of EHMT2. Subsequently, TNFAIP1 upregulation induced the apoptosis of CRC cells. Furthermore, using Bacteroides thetaiotaomicron culture medium, we confirmed EHMT2 downregulation via upregulation of HECTD2 and TNFAIP1 upregulation. Finally, we observed the synergistic effect of propionate and an EHMT2 inhibitor (BIX01294) in 3D spheroid culture models. Thus, we suggest the anticancer effects of propionate and EHMT2 as therapeutic targets for colon cancer treatment and may provide the possibility for the synergistic effects of an EHMT2 inhibitor and microbiome in CRC treatment.

Indexed as

Colorectal NeoplasmsMicrobiotaHistocompatibility AntigensHistone-Lysine N-MethyltransferaseHumansPropionatesUbiquitin-Protein LigasesUp-RegulationEHMT2 protein, humanHECTD2 protein, humanHistocompatibility AntigensHistone-Lysine N-MethyltransferasePropionatesUbiquitin-Protein Ligases

Identifiers

PMID34972816
PMCPMC9038766
OpenAlexW4205961267

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.