Evidence map›Paper›PMID 26722462›Full record

ArticleInternational journal of clinical and experimental pathology2015

miR-34c-3p inhibits cell proliferation, migration and invasion of hepatocellular carcinoma by targeting MARCKS.

Jianjun Song, Qi Wang, Yongyun Luo, Peng Yuan, Chaofeng Tang, Yongfeng Hui, Zuozheng Wang

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
0.9field-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

17 citing papers in PubMed, 33 citations in OpenAlex.

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  13. MARCKS and Lung Disease.American journal of respiratory cell and molecular biology · 2019
    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

7 authors at 1 institution in 1 country.

Jianjun SongDepartment of Hepatobiliary Surgery, General Hospital of Ningxia Medical University Yinchuan 750004, PR China.
Qi WangDepartment of Hepatobiliary Surgery, General Hospital of Ningxia Medical University Yinchuan 750004, PR China.
Yongyun LuoDepartment of Hepatobiliary Surgery, General Hospital of Ningxia Medical University Yinchuan 750004, PR China.
Peng YuanDepartment of Hepatobiliary Surgery, General Hospital of Ningxia Medical University Yinchuan 750004, PR China.
Chaofeng TangDepartment of Hepatobiliary Surgery, General Hospital of Ningxia Medical University Yinchuan 750004, PR China.
Yongfeng HuiDepartment of Hepatobiliary Surgery, General Hospital of Ningxia Medical University Yinchuan 750004, PR China.
Zuozheng WangDepartment of Hepatobiliary Surgery, General Hospital of Ningxia Medical University Yinchuan 750004, PR China.
Ningxia Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent studies have shown that microRNA-34c-3p (miR-34c-3p) is down-regulated in various types of cancers and involved in tumor growth, invasion and metastasis. However, the roles of miR-34c-3p in hepatocellular carcinoma (HCC) are poorly understood. In this study, the expression profile of miR-34c-3pin HCC tissues and cell lines were examined by quantitative real-time polymerase chain reaction (qRT-PCR). The correlations of miR-34c-3p expression and clinicopathological characteristics were analyzed. The biological role of MiR-34c-3pin cell proliferation, migration and invasion was examined. In addition, the targets of miR-34c-3p were identified. The results showed that miR-34c-3p expression was significantly down-regulated in HCC tissues and cell lines; low expression level of miR-34c-3p was correlated with vascular invasion and advanced TNM stage. In vitro functional assays showed that overexpression of miR-34c-3pin HepG2 and Huh7 cells significantly reduced cell proliferation, migration and invasion. Furthermore, target analysis and luciferase assay identified myristoylated alanine-rich protein kinase c substrate (MARCKS) as a specific target of miR-34c-3p. Knockdown of MARCKS in HepG2 cells reduced cell migration and invasion, but not cell proliferation. Taken together, our findings implicate the potential application of miR-34c-3p as a tumor suppressor in cancer therapy.

Indexed as

Carcinoma, HepatocellularCell MovementCell ProliferationFemaleHumansIntracellular Signaling Peptides and ProteinsLiver NeoplasmsMaleMembrane ProteinsMicroRNAsMiddle AgedMyristoylated Alanine-Rich C Kinase SubstrateNeoplasm InvasivenessNeoplasm StagingIntracellular Signaling Peptides and ProteinsMARCKS protein, humanMembrane ProteinsMicroRNAsMIRN34 microRNA, humanMyristoylated Alanine-Rich C Kinase Substratehepatocellular carcinomaMARCKSMiR-34c-3ptumor suppressor

Identifiers

PMID26722462
PMCPMC4680407
OpenAlexW2417441233

What OpenQuestion holds

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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.