Evidence map›Paper›PMID 30390677›Full record

ArticleDiagnostic pathology2018

MYO18B promotes hepatocellular carcinoma progression by activating PI3K/AKT/mTOR signaling pathway.

Zhenyu Zhang, Jinfeng Zhu, Yansong Huang, Weibing Li, Hongqiu Cheng

Open access · goldAbstract read
In one paragraph

Article in Diagnostic pathology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.6field-weighted citation impact, top 13% 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

14 citing papers in PubMed, 24 citations in OpenAlex.

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  13. A Traditional Chinese Medicine, Maoto, Suppresses Hepatitis B Virus Production.Frontiers in cellular and infection microbiology · 2020
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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

5 authors at 4 institutions in 1 country.

Zhenyu ZhangDepartment of Traditional Chinese Medicine, Shenzhen Pingshan District People's Hospital, Shenzhen, China.
Jinfeng ZhuDepartment of Traditional Chinese Medicine, Nantong Hospital of Traditional Chinese Medicine, Nantong, China.
Yansong HuangDepartment of Infectious Diseases, The Second Affiliated Hospital of Shantou University Medical College, NO. 69 Dongxia North Road, Shantou, 515041, People's Republic of China.
Weibing LiDepartment of Infectious Diseases, The Second Affiliated Hospital of Shantou University Medical College, NO. 69 Dongxia North Road, Shantou, 515041, People's Republic of China.
Hongqiu ChengDepartment of Infectious Diseases, The Second Affiliated Hospital of Shantou University Medical College, NO. 69 Dongxia North Road, Shantou, 515041, People's Republic of China. 982115479@qq.com.
Second Affiliated Hospital of Shantou University Medical College · CNAnyang Hospital of Traditional Chinese Medicine · CNShantou University · CNShenzhen Pingle Orthopedic Hospital · CN

Funding

Joint Scientific Special foundation of Guangdong Provincial Department of Science and Technology-Academy of Traditional Chinese Medicine 2013A032500017
6 · The paper itself

Abstract

backgroundMYO18B has been identified as a novel tumor suppressor gene in several cancers. However, its specific roles in the progression of hepatocellular carcinoma (HCC) has not been well defined.

methodsWe firstly identified the expression and prognostic values of MYO18B in HCC using TCGA cohort and our clinical data. Then, MYO18B knockdown by RNA inference was implemented to investigate the effects of MYO18B on HCC cells. Quantitative RT-PCR and Western blot were used to determine gene and protein expression levels. CCK-8 and colony formation assays were performed to examine cell proliferation capacity. Wound healing and transwell assays were used to evaluate the migration and invasion of HepG2 cells.

resultsMYO18B was overexpressed and correlated with poor prognosis in HCC. MYO18B expression was an independent risk factor for overall survival. Knockdown of MYO18B significantly inhibited the proliferation, migration and invasion of HepG2 cells. Meanwhile, MYO18B knockdown could effectively suppress the phosphorylation of PI3K, AKT, mTOR and P70S6K, suggesting that MYO18B might promote HCC progression by targeting PI3K/AKT/mTOR signaling pathway.

conclusionsMYO18B promoted tumor growth and migration via the activation of PI3K/AKT/mTOR signaling pathway. MYO18B might be a promising target for clinical intervention of HCC.

Indexed as

Signal TransductionCarcinoma, HepatocellularCell MovementCell ProliferationDisease ProgressionFemaleGene Expression Regulation, NeoplasticHep G2 CellsHumansLiver NeoplasmsMaleMiddle AgedMyosinsNeoplasm InvasivenessPhosphatidylinositol 3-KinasePhosphorylationMTOR protein, humanMYO18B protein, humanMyosinsPhosphatidylinositol 3-KinaseProto-Oncogene Proteins c-aktTOR Serine-Threonine KinasesTumor Suppressor ProteinsHepatocellular carcinomaMYO18BPI3K/AKT/mTOR signaling pathwayPrognosis

Identifiers

PMID30390677
PMCPMC6215340
OpenAlexW2899204875

What OpenQuestion holds

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LicenceCC BY
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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.