Evidence map›Paper›PMID 32164722›Full record

ArticleMolecular cancer2020

CircMRPS35 suppresses gastric cancer progression via recruiting KAT7 to govern histone modification.

Mengmeng Jie, Yaran Wu, Mengyuan Gao, Xinzhe Li, Cheng Liu, Qin Ouyang, Qingyun Tang, Changyu Shan, Yangfan Lv, Kebin Zhang and 8 more

Open access · goldAbstract read
In one paragraph

Article in Molecular cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 115 papers.

0numbers the graph read from it
0cells of the map it votes in
115citing papers in PubMed
11.3field-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

115 citing papers in PubMed, 181 citations in OpenAlex.

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  20. The role of acetylation and deacetylation in cancer metabolism.Clinical and translational medicine · 2025
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55 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

18 authors at 2 institutions in 1 country.

Mengmeng JieDepartment of Gastroenterology, Xinqiao Hospital, Third Military Medical University, Chongqing, 400037, China.
Yaran WuDepartment of Gastroenterology, Xinqiao Hospital, Third Military Medical University, Chongqing, 400037, China.
Mengyuan GaoDepartment of Gastroenterology, Xinqiao Hospital, Third Military Medical University, Chongqing, 400037, China.
Xinzhe LiDepartment of Gastroenterology, Xinqiao Hospital, Third Military Medical University, Chongqing, 400037, China.
Cheng LiuDepartment of Gastroenterology, Xinqiao Hospital, Third Military Medical University, Chongqing, 400037, China.
Qin OuyangDepartment of Medicinal Chemistry, College of Pharmacy, Third Military Medical University, Chongqing, 400038, China.
Qingyun TangDepartment of Gastroenterology, Xinqiao Hospital, Third Military Medical University, Chongqing, 400037, China.
Changyu ShanDepartment of Medicinal Chemistry, College of Pharmacy, Third Military Medical University, Chongqing, 400038, China.
Yangfan LvDepartment of Pathology, Xinqiao Hospital, Third Military Medical University, Chongqing, 400037, China.
Kebin ZhangCentral Laboratory, Xinqiao Hospital, Third Military Medical University, Chongqing, 400037, China.
Qian DaiCentral Laboratory, Xinqiao Hospital, Third Military Medical University, Chongqing, 400037, China.
Yang ChenDepartment of Gastroenterology, Xinqiao Hospital, Third Military Medical University, Chongqing, 400037, China.
Shuo ZengDepartment of Gastroenterology, Xinqiao Hospital, Third Military Medical University, Chongqing, 400037, China.
Chenglin LiDepartment of Gastroenterology, Xinqiao Hospital, Third Military Medical University, Chongqing, 400037, China.
Liting WangBiomedical Analysis Center, Third Military Medical University, Chongqing, 400038, China.
Fengtian HeDepartment of Biochemistry and Molecular Biology, College of Basic Medical Sciences, Third Military Medical University, Chongqing, 400038, China.
Changjiang HuDepartment of Gastroenterology, Xinqiao Hospital, Third Military Medical University, Chongqing, 400037, China. hcj_888@126.com.
Shiming YangDepartment of Gastroenterology, Xinqiao Hospital, Third Military Medical University, Chongqing, 400037, China. Yangshiming@tmmu.edu.cn.
Army Medical University · CNXinqiao Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAberrant expression of circular RNAs contributes to the initiation and progression of cancers, but the underlying mechanism remains elusive.

methodsRNA-seq and qRT-PCR were performed to screen differential expressed circRNAs between gastric cancer tissues and adjacent normal tissues. Candidate circRNA (circMRPS35) was screened out and validated by qRT-PCR. Cell proliferation and invasion ability were determined by CCK-8 and cell invasion assays. RNA-seq, GO-pathway, RNA pull-down and ChIRP were further applied to search for detailed mechanism.

resultsHere, a novel circRNA named circMRPS35, was screened out by RNA-seq in gastric cancer tissues, whose expression is related to clinicopathological characteristics and prognosis in gastric cancer patients. Biologically, circMRPS35 suppresses the proliferation and invasion of gastric cancer cells in vitro and in vivo. Mechanistically, circMRPS35 acts as a modular scaffold to recruit histone acetyltransferase KAT7 to the promoters of FOXO1 and FOXO3a genes, which elicits acetylation of H4K5 in their promoters. Particularly, circMRPS35 specifically binds to FOXO1/3a promoter regions directly. Thus, it dramatically activates the transcription of FOXO1/3a and triggers subsequent response of their downstream target genes expression, including p21, p27, Twist1 and E-cadherin, resulting in the inhibition of cell proliferation and invasion. Moreover, circMRPS35 expression positively correlates with that of FOXO1/3a in gastric cancer tissues.

conclusionsOur findings not only reveal the pivotal roles of circMRPS35 in governing histone modification in anticancer treatment, but also advocate for triggering circMRPS35/KAT7/FOXO1/3a pathway to combat gastric cancer.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsApoptosisBiomarkers, TumorCell ProliferationDisease ProgressionForkhead Box Protein O1Forkhead Box Protein O3Histone AcetyltransferasesHistonesHumansMiceMice, NudePrognosisProtein Processing, Post-TranslationalRNA, CircularBiomarkers, TumorForkhead Box Protein O1Forkhead Box Protein O3FOXO1 protein, humanFOXO3 protein, humanHistone AcetyltransferasesHistonesKAT7 protein, humanRNA, CircularAcetylationCircular RNAGastric cancerHistone modification

Identifiers

PMID32164722
PMCPMC7066857
OpenAlexW3012353633

What OpenQuestion holds

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LicenceCC BY
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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.