Evidence map›Paper›PMID 31466138›Full record

ArticleCancer medicine2019

miR-124-3p availability is antagonized by LncRNA-MALAT1 for Slug-induced tumor metastasis in hepatocellular carcinoma.

Rong-Jun Cui, Jia-Lin Fan, Yu-Cui Lin, Yu-Jia Pan, Chi Liu, Jia-Hui Wan, Wei Wang, Zheng-Yuan Jiang, Xiu-Lan Zheng, Jie-Bing Tang and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 11% 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

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 40 citations in OpenAlex.

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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 at 2 institutions in 1 country.

Rong-Jun CuiDepartment of Biochemistry and Molecular Biology, Harbin Medical University, Harbin, Heilongjiang, China.ORCID 0000-0003-1052-8821
Jia-Lin FanDepartment of Biochemistry and Molecular Biology, Harbin Medical University, Harbin, Heilongjiang, China.
Yu-Cui LinDepartment of Biochemistry and Molecular Biology, Harbin Medical University, Harbin, Heilongjiang, China.
Yu-Jia PanDepartment of Biochemistry and Molecular Biology, Harbin Medical University, Harbin, Heilongjiang, China.
Chi LiuDepartment of Biochemistry and Molecular Biology, Harbin Medical University, Harbin, Heilongjiang, China.
Jia-Hui WanDepartment of Biochemistry and Molecular Biology, Mudanjiang Medical University, Mudanjiang, Heilongjiang, China.ORCID 0000-0002-6430-5562
Wei WangDepartment of Biochemistry and Molecular Biology, Harbin Medical University, Harbin, Heilongjiang, China.
Zheng-Yuan JiangDepartment of Biochemistry and Molecular Biology, Harbin Medical University, Harbin, Heilongjiang, China.
Xiu-Lan ZhengDepartment of Ultrasonography, Harbin Medical University Cancer Hospital, Harbin, Heilongjiang, China.
Jie-Bing TangDepartment of Gastrointestinal Medical Oncology, Harbin Medical University Cancer Hospital, Harbin, Heilongjiang, China.
Xiao-Guang YuDepartment of Biochemistry and Molecular Biology, Harbin Medical University, Harbin, Heilongjiang, China.
Harbin Medical University · CNMudanjiang Medical University · CN

Funding

Postdoctoral Scientific Research Developmental Fund of Heilongjiang Province LBH-Q16147Postgraduate Innovation Research Project of Mudanjiang Medical University 2017YJSCX-04MY
6 · The paper itself

Abstract

backgroundAs an oncogene, long noncoding RNA metastasis-associated lung adenocarcinoma transcript 1 (MALAT1) can promote tumor metastasis. Hyperexpression of MALAT1 has been observed in many malignant tumors, including hepatocellular carcinoma (HCC). However, the role and mechanism of MALAT1 in HCC remain unclear.

methodsThirty human HCC and paracancerous tissue specimens were collected, and the human hepatoma cell lines Huh7 and HepG2 were cultured according to standard methods. MALAT1 and Snail family zinc finger (Slug) expression were measured by real-time PCR, immunohistochemistry, and western blotting. Luciferase reporter assay and RNA immunoprecipitation (RIP) assay verified the direct interaction between miR-124-3p and Slug(SNAI2) or MALAT1. Wound healing and transwell assays were performed to examine invasion and migration, and a subcutaneous tumor model was established to measure tumor progression in vivo.

resultsMALAT1 expression was upregulated in HCC tissues and positively correlated with Slug expression. MALAT1 and miR-124-3p bind directly and reversibly to each other. MALAT1 silencing inhibited cell migration and invasion. miR-124-3p inhibited HCC metastasis by targeting Slug.

conclusionsMALAT1 regulates Slug through miR-124-3p, affecting HCC cell metastasis. Thus, the MALAT1/miR-124-3p/Slug axis plays an important role in HCC.

Indexed as

Gene Expression Regulation, NeoplasticAdultAgedAnimalsCarcinoma, HepatocellularCell Line, TumorDisease Models, AnimalFemaleGene Knockdown TechniquesHumansImmunohistochemistryLiver NeoplasmsMaleMiceMicroRNAsMiddle AgedMALAT1 long non-coding RNA, humanMicroRNAsMIRN124 microRNA, humanRNA, Long NoncodingSNAI1 protein, humanSnail Family Transcription Factorshepatocellular carcinomametastasis-associated lung adenocarcinoma transcript 1miR-124-3ptumor metastasis

Identifiers

PMID31466138
PMCPMC6797582
OpenAlexW2970769782

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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.