Evidence map›Paper›PMID 37789393›Full record

ArticleMolecular cancer2023

LINC00922 decoys SIRT3 to facilitate the metastasis of colorectal cancer through up-regulation the H3K27 crotonylation of ETS1 promoter.

Meijian Liao, Xiaolin Sun, Wendan Zheng, Mengdi Wu, Yifan Wang, Jia Yao, Yu Ma, Shoucui Gao, Dongsheng Pei

Open access · goldAbstract read
In one paragraph

Article in Molecular cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
8.6field-weighted citation impact, top 2% 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

43 citing papers in PubMed, 48 citations in OpenAlex.

  1. Integrative omics profiling of CRELD2 in ccRCC: a nexus of genetics, prognosis, and tumor microenvironment.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
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  7. The Landscape and Regulation of Histone Crotonylation in Mammalian Gametes and Early Embryos.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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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

9 authors at 1 institution in 1 country.

Meijian Liao *Department of Pathology, Xuzhou Medical University, Xuzhou, 221004, P.R. China.
Xiaolin Sun *Department of Pathology, Xuzhou Medical University, Xuzhou, 221004, P.R. China.
Wendan ZhengDepartment of Pathology, Xuzhou Medical University, Xuzhou, 221004, P.R. China.
Mengdi WuDepartment of Pathology, Xuzhou Medical University, Xuzhou, 221004, P.R. China.
Yifan WangDepartment of Pathology, Xuzhou Medical University, Xuzhou, 221004, P.R. China.
Jia YaoDepartment of Pathology, Xuzhou Medical University, Xuzhou, 221004, P.R. China.
Yu MaDepartment of Pathology, Xuzhou Medical University, Xuzhou, 221004, P.R. China.
Shoucui GaoDepartment of Pathology, Xuzhou Medical University, Xuzhou, 221004, P.R. China. gaoshoucui@xzhmu.edu.cn.
Dongsheng PeiDepartment of Pathology, Xuzhou Medical University, Xuzhou, 221004, P.R. China. dspei@xzhmu.edu.cn.
Xuzhou Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLysine crotonylation (Kcr) is up-regulation in colorectal cancer (CRC) tissues, while its specific contribution remains uncertain. This study aimed to elucidate the role and mechanism of crotonylation on Lys27 of histone H3 (H3K27cr) in facilitating CRC metastasis.

methodsImmunohistochemistry was employed to investigate the correlation between H3K27cr and CRC metastasis. Both in vitro and in vivo assays employing loss function or gain function approaches were conducted to elucidate the role of LINC00922 in promoting CRC metastasis. ScRNA-seq analysis and immunoprecipitation analyses were employed to explore the underlying mechanism by which LINC00922 facilitates CRC metastasis through H3K27cr.

resultsClinically, H3K27cr was upregulated in metastatic CRC tissues and positively correlated with advanced clinical stages. Functionally, knockdown of LINC00922 inhibited migration of CRC cells both in vitro and in vivo. Furthermore, the supplementation of NaCr restored the migration and invasion levels of LINC00922 stable knockdown cells by restoring the H3K27cr level. Mechanistically, LINC00922 promoted invasion and migration through H3K27cr mediated cell adhesion molecules (CAMs) in epithelial cells. Notably, LINC00922 interacted with the protein sirtuin 3 (SIRT3) and obstructed its binding to the promoter region of ETS1, leading to an elevation in the level of H3K27cr in this promoter region and the subsequent activation of ETS1 transcription.

conclusionsOur findings uncovered a novel regulatory function of H3K27cr, regulated by LINC00922, in facilitating CRC metastasis. This discovery contributed to a deeper comprehension of the involvement of histone crotonylation in the metastatic process of CRC.

Indexed as

Colorectal NeoplasmsSirtuin 3Cell Line, TumorCell MovementCell ProliferationGene Expression Regulation, NeoplasticHistonesHumansNeoplasm MetastasisPromoter Regions, GeneticProto-Oncogene Protein c-ets-1Transcriptional ActivationUp-RegulationETS1 protein, humanHistonesProto-Oncogene Protein c-ets-1SIRT3 protein, humanSirtuin 3Colorectal cancerH3K27crLINC00922MetastasisSIRT3

Identifiers

PMID37789393
PMCPMC10548613
OpenAlexW4387326192

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.