Evidence map›Paper›PMID 34880125›Full record

ArticleMolecular cancer research : MCR2022

Epigenetic Silencing of 15-Hydroxyprostaglandin Dehydrogenase by Histone Methyltransferase EHMT2/G9a in Cholangiocarcinoma.

Jinqiang Zhang, Weina Chen, Wenbo Ma, Kyoungsub Song, Sean Lee, Chang Han, Tong Wu

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cancer research : MCR, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

6 citing papers in PubMed, 13 citations in OpenAlex.

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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

7 authors at 1 institution in 1 country.

Jinqiang ZhangDepartment of Pathology and Laboratory Medicine, Tulane University School of Medicine, New Orleans, Louisiana.ORCID 0000-0001-9594-276X
Weina ChenDepartment of Pathology and Laboratory Medicine, Tulane University School of Medicine, New Orleans, Louisiana.ORCID 0000-0002-8290-7049
Wenbo MaDepartment of Pathology and Laboratory Medicine, Tulane University School of Medicine, New Orleans, Louisiana.
Kyoungsub SongDepartment of Pathology and Laboratory Medicine, Tulane University School of Medicine, New Orleans, Louisiana.
Sean LeeDepartment of Pathology and Laboratory Medicine, Tulane University School of Medicine, New Orleans, Louisiana.
Chang HanDepartment of Pathology and Laboratory Medicine, Tulane University School of Medicine, New Orleans, Louisiana.
Tong WuDepartment of Pathology and Laboratory Medicine, Tulane University School of Medicine, New Orleans, Louisiana.
Tulane University · US

Funding

cPLA2, COX-2 and PPAR-gamma in CholangiocarcinomaR01CA102325 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI WU, TONG · 2005 to 2020
$3.8M
Epigenetic Mechanisms of Biliary Epithelial NeoplasiaR01CA219541 · NCI · TULANE UNIVERSITY OF LOUISIANA · PI Tong Wu · 2018 to 2026
$2.4M
The Long Noncoding RNA MALAT1 in Liver CancerR01CA226281 · NCI · TULANE UNIVERSITY OF LOUISIANA · PI WU, TONG · 2019 to 2023
$1.7M
NCI NIH HHS R01 CA102325NCI NIH HHS R01 CA219541NCI NIH HHS R01 CA226281
6 · The paper itself

Abstract

Cholangiocarcinoma (CCA) is a lethal malignancy with few therapeutic options. NAD+-dependent 15-hydroxyprostaglandin dehydrogenase (15-PGDH) has been shown to inhibit CCA cell growth in vitro and in xenograft models. However, the role of 15-PGDH in CCA development has not been investigated and the mechanism for 15-PGDH gene regulation remains unclear. Here, we evaluated the role of 15-PGDH in CCA development by using a mouse model with hydrodynamic tail vein injection of transposase-based plasmids expressing Notch1 intracellular domain and myr-Akt, with or without co-injection of 15-PGDH expression plasmids. Our results reveal that 15-PGDH overexpression effectively prevents CCA development. Through patient data mining and experimental approaches, we provide novel evidences that 15-PGDH is epigenetically silenced by histone methyltransferase G9a. We observe that 15-PGDH and G9a expressions are inversely correlated in both human and mouse CCAs. By using CCA cells and mouse models, we show that G9a inhibition restores 15-PGDH expression and inhibited CCA in vitro and in vivo. Mechanistically, our data indicate that G9a is recruited to 15-PGDH gene promoter via protein-protein interaction with the E-box binding Myc/Max heterodimer. The recruited G9a then silences 15-PGDH gene through enhanced methylation of H3K9. Our further experiments have led to the identification of STAT4 as a key transcription factor involved in the regulation of 15-PGDH by G9a. Collectively, our findings disclose a novel G9a-15PGDH signaling axis which is importantly implicated in CCA development and progression. IMPLICATIONS: The current study describes a novel G9a-15PGDH signaling axis which is importantly implicated in CCA development and progression.

Indexed as

Bile Duct NeoplasmsCholangiocarcinomaBile Ducts, IntrahepaticEpigenesis, GeneticHistocompatibility AntigensHistone-Lysine N-MethyltransferaseHistone MethyltransferasesHumansHydroxyprostaglandin Dehydrogenases15-hydroxyprostaglandin dehydrogenaseEHMT2 protein, humanHistocompatibility AntigensHistone-Lysine N-MethyltransferaseHistone MethyltransferasesHydroxyprostaglandin Dehydrogenases

Identifiers

PMID34880125
PMCPMC8898302
OpenAlexW4200433772

What OpenQuestion holds

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Registered trials

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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.