Evidence map›Paper›PMID 32194906›Full record

ArticleAmerican journal of translational research2020

LncRNA FLJ33360 accelerates the metastasis in hepatocellular carcinoma by targeting miRNA-140/MMP9 axis.

Zhenhui Lu, Yingzi Yu, Xiangchun Ding, Dong Jin, Genwang Wang, Yu Zhou, Yongzhao Zhu, Li Na, Yaqin He, Qi Wang

Open access · greenAbstract read
In one paragraph

Article in American journal of translational research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.1field-weighted citation impact, top 26% 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

15 citing papers in PubMed, 17 citations in OpenAlex.

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  4. Role of miR-498 Combined with CREB1 in Apoptosis and Invasion of Hepatoma Cell Line.Computational and mathematical methods in medicine · 2022
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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

10 authors at 1 institution in 1 country.

Zhenhui LuDepartment of Hepatobiliary Surgery, General Hospital of Ningxia Medical University Yinchuan, Ningxia, China.
Yingzi YuDepartment of Infection Control, General Hospital of Ningxia Medical University Yinchuan, Ningxia, China.
Xiangchun DingDepartment of Infectious Disease, General Hospital of Ningxia Medical University Yinchuan, Ningxia, China.
Dong JinDepartment of Hepatobiliary Surgery, General Hospital of Ningxia Medical University Yinchuan, Ningxia, China.
Genwang WangDepartment of Hepatobiliary Surgery, General Hospital of Ningxia Medical University Yinchuan, Ningxia, China.
Yu ZhouDepartment of Surgical Research Laborator, General Hospital of Ningxia Medical University Yinchuan, Ningxia, China.
Yongzhao ZhuDepartment of Surgical Research Laborator, General Hospital of Ningxia Medical University Yinchuan, Ningxia, China.
Li NaDepartment of Surgical Research Laborator, General Hospital of Ningxia Medical University Yinchuan, Ningxia, China.
Yaqin HeDepartment of Surgical Research Laborator, General Hospital of Ningxia Medical University Yinchuan, Ningxia, China.
Qi WangDepartment of Hepatobiliary Surgery, General Hospital of Ningxia Medical University Yinchuan, Ningxia, China.
Ningxia Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study aims to detect expression level of long non-coding RNA (lncRNA) FLJ33360 in hepatocellular carcinoma (HCC) and its regulatory effects on accelerating malignant progression of HCC. Expression levels of FLJ33360 in 29 matched HCC tissues and paracancerous tissues were detected by quantitative real-time polymerase chain reaction (qRT-PCR). After transfection of sh-FLJ33360#1 in Bel-7402 and HepG2 cells, changes in migratory and invasive capacities were evaluated by Transwell and wound healing assay. Potential miRNAs targeting FLJ33360 were verified. The correlation between expression levels of FLJ33360 and miRNA-140 in HCC tissues was determined. At last, potential influences of FLJ33360/miRNA-140 regulatory loop on HCC phenotypes were determined by rescue experiments. FLJ33360 was upregulated in HCC tissues relative to paracancerous ones. After knockdown of FLJ33360, migratory and invasive capacities in Bel-7402 and HepG2 cells were attenuated. There were five miRNA candidates predicted to bind FLJ33360, and miRNA-140 was the most differentially expressed by FLJ33360 regulation. Dual-luciferase reporter gene assay confirmed the binding between FLJ33360 and miRNA-140. Besides, their expression levels were negatively correlated in HCC tissues. Moreover, knockdown of miRNA-140 could stimulate metastatic ability in HCC. At last, rescue experiments verified the involvement of miRNA-140 in FLJ33360-regulated HCC progression. LncRNA FLJ33360 is upregulated in HCC. It accelerates the metastasis of HCC through targeting miRNA-140/MMP9 axis.

Indexed as

FLJ33360hepatocellular carcinoma (HCC)metastasismiRNA-140

Identifiers

PMID32194906
PMCPMC7061837
OpenAlexW3012580769

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.