Evidence map›Paper›PMID 31270046›Full record

ArticleNan fang yi ke da xue xue bao = Journal of Southern Medical University2019

[Long noncoding RNA UFC1 promotes metastasis and invasion of hepatocellular carcinoma cells

Jian Wang, Chuanhui Cao, Qin Zeng, Zhongyi Dong

Abstract read
In one paragraph

Article in Nan fang yi ke da xue xue bao = Journal of Southern Medical University, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 91% of its field
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Jian WangDepartment of Radiation Oncology, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China.
Chuanhui CaoDepartment of Radiation Oncology, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China.
Qin ZengDepartment of Radiation Oncology, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China.
Zhongyi DongDepartment of Radiation Oncology, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China.
Nanfang Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo explore the role of Long noncoding RNA UFC1 (lincRNA-UFC1) in modulating the metastasis and invasion of hepatocellular carcinoma (HCC) cells and the underlying mechanism.

methodsHuman HCC cell line Huh7 was infected with the lentiviral vector carrying lincRNA-UFC1 to obtain a cell line with lincRNA-UFC1 overexpression. A short hairpin RNA (shRNA) targeting lincRNA-UFC1 was delivered in human HCC BEL-7402 cells via a lentiviral vector to obtain a cell line with lincRNA-UFC1 knockdown. Expression levels of lincRNA-UFC1 in the two HCC cell lines were detected using real-time PCR, and the changes in the cell invasion and migration in response to lincRNA-UFC1 overexpression or knockdown were analyzed using Transwell and wound-healing assays. The expressions of GSK-3β/β-catenin-related proteins in the cells were detected with Western blotting. XAV-939, a GSK-3β/β-catenin inhibitor, was used for assessing the impact of lincRNAUFC1 overexpression on the invasion and migration of the HCC cells through Transwell and wound-healing assays.

resultsOverexpression of lincRNA-UFC1 significantly promoted the invasion and migration of Huh7 cells as compared with the control cells (

conclusionslincRNA-UFC1 overexpresison promotes cell invasion and migration through the GSK-3β/β-catenin axis in HCC cells

Indexed as

Carcinoma, HepatocellularLiver Neoplasmsbeta CateninCell Line, TumorGlycogen Synthase Kinase 3 betaHumansNeoplasm InvasivenessNeoplasm MetastasisRNA, Long Noncodingbeta CateninCTNNB1 protein, humanGlycogen Synthase Kinase 3 betaRNA, Long Noncodinghepatocellular carcinomalincRNA-UFC1p-GSK3tumor progressionβ-catenin

Identifiers

PMID31270046
PMCPMC6743920
OpenAlexW2962949296

What OpenQuestion holds

Textmetadata
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.