Evidence map›Paper›PMID 31273190›Full record

ArticleCell death & disease2019

Long noncoding RNA SNHG14 facilitates colorectal cancer metastasis through targeting EZH2-regulated EPHA7.

Wu Di, Xue Weinan, Li Xin, Yu Zhiwei, Gu Xinyue, Tong Jinxue, Li Mingqi

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed, 1 pooled it
6.1field-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

63 citing papers in PubMed, 1 synthesis or guideline pooled it, 108 citations in OpenAlex.

  1. Pooled it
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  16. Journal of gastrointestinal oncology · 2023
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  19. The role of EphA7 in different tumors.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2022
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3 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

7 authors at 4 institutions in 1 country.

Wu DiDepartment of Colorectal Surgery, Harbin Medical University Cancer Hospital, Harbin, China.
Xue WeinanDepartment of Colorectal Surgery, Harbin Medical University Cancer Hospital, Harbin, China.
Li XinDepartment of Cardiology, The Fourth Affiliated Hospital of Harbin Medical University, Harbin, China.
Yu ZhiweiDigestive System Diseases Center, The Seventh Affiliated Hospital of Sun Yat-sen University, Guangzhou Shi, China.
Gu XinyueDepartment of Colorectal Surgery, Harbin Medical University Cancer Hospital, Harbin, China.
Tong JinxueDepartment of Colorectal Surgery, Harbin Medical University Cancer Hospital, Harbin, China.
Li MingqiDepartment of Colorectal Surgery, Harbin Medical University Cancer Hospital, Harbin, China. shepherdli@126.com.
Harbin Medical University · CNFourth Affiliated Hospital of Harbin Medical University · CNThe Seventh Affiliated Hospital of Sun Yat-sen University · CNThird Affiliated Hospital of Harbin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Accumulating evidence suggested the participation of long noncoding RNAs (lncRNAs) in regulating various biological processes so as to affecting cancer progression. However, the functional role of most lncRNAs in colorectal carcer (CRC) is still largely covered. In the present study, we disclosed SNHG14 as a carcinogene in CRC development, as it was low-expressed in normal colon tissues but markedly upregulated in CRC cell lines. Besides, SNHG14 contributed to CRC cell proliferation, motility and EMT in vitro, and inhibition of it confined CRC tumor growth and liver metastasis in vivo. Next, the mechanistic investigations confirmed that SNHG14-promoted CRC progression was mediated by EPHA7, which was negatively regulated by SNHG14 in CRC via an EZH2-dependent way. Importantly, EZH2 was proved as a transcription factor of EPHA7 and functioned as a repressor in EPHA7 transcription by enhancing methylation on EPHA7 promoter. Meanwhile, SNHG14 increased EZH2 expression in CRC via stabilizing its mRNA by interacting with FUS, and via freeing its mRNA from miR-186-5p-induced silence. All in all, our observations demonstrated that SNHG14 serves as a facilitator in CRC through targeting EZH2-repressed EPHA7 by enhancing EZH2 via recruiting FUS and absorbing miR-186-5p, indicating a promising new road for CRC diagnosis and treatment.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsBase SequenceCell Line, TumorCell ProliferationColorectal NeoplasmsDisease ProgressionEnhancer of Zeste Homolog 2 ProteinEpigenesis, GeneticGene SilencingHumansMice, Inbred BALB CMice, NudeModels, BiologicalMutationNeoplasm MetastasisEnhancer of Zeste Homolog 2 ProteinEZH2 protein, humanFUS protein, humanReceptor, EphA7RNA-Binding Protein FUSRNA, Long NoncodingRNA, Messenger

Identifiers

PMID31273190
PMCPMC6609685
OpenAlexW2955185508

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.