Evidence map›Paper›PMID 39349460›Full record

ArticleCell death & disease2024

LINC00887 promotes GCN5-dependent H3K27cr level and CRC metastasis via recruitment of YEATS2 and enhancing ETS1 expression.

Meijian Liao, Wendan Zheng, Yifan Wang, Mengting Li, Xiaolin Sun, Nan Liu, Jia Yao, Fuxing Dong, Qingling Wang, Yu Ma and 1 more

Abstract read
In one paragraph

Article in Cell death & disease, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
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

10 citing papers in PubMed.

  1. Article
  2. Review
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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

11 authors.

Meijian Liao *Department of Pathology, Xuzhou Medical University, Xuzhou, 221004, PR China.
Wendan Zheng *Department of Pathology, Xuzhou Medical University, Xuzhou, 221004, PR China.
Yifan WangDepartment of Pathology, Xuzhou Medical University, Xuzhou, 221004, PR China.
Mengting LiDepartment of Pathology, Xuzhou Medical University, Xuzhou, 221004, PR China.
Xiaolin SunDepartment of Pathology, Xuzhou Medical University, Xuzhou, 221004, PR China.
Nan LiuDepartment of Infectious Diseases and Center of Infectious Diseases and Pathogen Biology, the First Hospital of Jilin University, Changchun, 130061, PR China.
Jia YaoDepartment of Pathology, Xuzhou Medical University, Xuzhou, 221004, PR China.
Fuxing DongPublic Experimental Research Center, Xuzhou Medical University, Xuzhou, 221004, PR China.
Qingling WangDepartment of Pathology, Xuzhou Medical University, Xuzhou, 221004, PR China.
Yu MaDepartment of Pathology, Xuzhou Medical University, Xuzhou, 221004, PR China. mayu@xzhmu.edu.cn.ORCID 0009-0009-5888-245X
Jie MouSchool of Pharmacy, Xuzhou Medical University, Xuzhou, 221004, PR China. mou.jie@xzhmu.edu.cn.ORCID 0000-0002-0952-4500

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent observations have revealed upregulation of H3K27cr in colorectal cancer (CRC) tissues; however, the underlying cause remains elusive. This study aimed to investigate the mechanism of H3K27cr upregulation and its roles in CRC metastasis. Clinically, our findings showed that H3K27cr served as a highly accurate diagnostic marker to distinguish CRC tissues from healthy controls. Elevated levels of LINC00887 and H3K27cr were associated with a poorer prognosis in CRC patients. Functionally, LINC00887 and H3K27cr facilitated the migration and invasion of CRC cells. Mechanistically, LINC00887 interacted with SIRT3 protein. Overexpressed of LINC00887 obstructed the enrichment of SIRT3 within GCN5 promoter, thereby elevating H3K27ac but not H3K27cr level within this region, subsequently activating GCN5 expression. This activation increased the global level of H3K27cr, promoting the enrichment of GCN5, H3K27cr, and YEATS2 within ETS1 promoter, activating ETS1 transcription and ultimately promoting the metastasis of CRC. The in vivo study demonstrated that inhibition of LINC00887 suppressed CRC metastasis, but this inhibitory effect was nullified when mice were treated with NaCr. In conclusion, our results confirmed the diagnostic biomarker potential of H3K27cr in individuals with CRC, and proposed a functional model to elucidate the involvement of LINC00887 in promoting CRC metastasis by elevating H3K27cr level.

Indexed as

Colorectal NeoplasmsGene Expression Regulation, NeoplasticMice, Nudep300-CBP Transcription FactorsProto-Oncogene Protein c-ets-1RNA, Long NoncodingAnimalsCell Line, TumorCell MovementFemaleHistonesHumansMaleMiceMice, Inbred BALB CMiddle AgedETS1 protein, humanHistonesp300-CBP-Associated Factorp300-CBP Transcription FactorsProto-Oncogene Protein c-ets-1RNA, Long NoncodingSirtuin 3

Identifiers

PMID39349460
PMCPMC11443008

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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.