Evidence map›Paper›PMID 25120775›Full record

ArticleInternational journal of clinical and experimental pathology2014

Knockdown of Aurora-B inhibits osteosarcoma cell invasion and migration via modulating PI3K/Akt/NF-κB signaling pathway.

Liang Bo Zhu, Jian Jiang, Xiao Ping Zhu, Tao Fang Wang, Xuan Yin Chen, Qin Feng Luo, Yong Shu, Zhi Li Liu, Shan Hu Huang

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.4field-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

31 citing papers in PubMed, 43 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

9 authors at 2 institutions in 1 country.

Liang Bo ZhuDepartment of Orthopedics, The First Affiliated Hospital of Nanchang University Jiangxi, China.
Jian JiangDepartment of Orthopedics, The First Affiliated Hospital of Nanchang University Jiangxi, China ; Department of Orthopedics, People's Hospital of Shangrao City Jiangxi, China.
Xiao Ping ZhuDepartment of Anesthesia, The First Affiliated Hospital of Nanchang University Jiangxi, China.
Tao Fang WangDepartment of Orthopedics, The First Affiliated Hospital of Nanchang University Jiangxi, China.
Xuan Yin ChenDepartment of Orthopedics, The First Affiliated Hospital of Nanchang University Jiangxi, China.
Qin Feng LuoDepartment of Pathology, Cancer Hospital of Jiangxi Province Jiangxi, China.
Yong ShuDepartment of Orthopedics, The First Affiliated Hospital of Nanchang University Jiangxi, China.
Zhi Li LiuDepartment of Orthopedics, The First Affiliated Hospital of Nanchang University Jiangxi, China.
Shan Hu HuangDepartment of Orthopedics, The First Affiliated Hospital of Nanchang University Jiangxi, China.
Nanchang University · CNJiangxi Provincial Cancer Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Increasing evidences reveal that Aurora-B may be involved in metastasis of malignant tumor. In this study, we investigated the inhibitory effect of Aurora-B on invasion and migration of OS cells and the activity of PI3K/Akt/NF-κB signaling pathway in vitro. The expression of Aurora-B and p-Akt (Ser473) proteins was detected by immunohistochemistry in OS tissues from 24 patients with pulmonary metastatic disease, and the relationship between Aurora-B and p-Akt was investigated. The results showed that there was a positive correlation between Aurora-B and p-Akt protein expression. Furthermore, we down-regulated the expression of Aurora-B through a recombinant lentivirus (Lv-shAURKB). Migration and invasion of cells were investigated by wound healing and transwell invasion assays. Results showed that silencing Aurora-B inhibited cell migratory and invasive ability of OS cells in vitro. Finally, knockdown of Aurora-B suppresses the activity of PI3K/Akt/NF-κB signaling pathway in OS cells. Our results indicated that knockdown of Aurora-B suppresses OS cells migratory and invasive ability via modulating the "PI3K/Akt/NF-κB" signaling pathway in vitro. The Aurora-B blocker may be a new therapeutic strategy in OS management.

Indexed as

Cell MovementAurora Kinase BBlotting, WesternBone NeoplasmsCell Line, TumorGene Knockdown TechniquesHumansImmunohistochemistryNeoplasm InvasivenessNF-kappa BOsteosarcomaPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktReal-Time Polymerase Chain ReactionReverse Transcriptase Polymerase Chain ReactionSignal TransductionAURKB protein, humanAurora Kinase BNF-kappa BPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktAurora-Binvasion and migrationOsteosarcomaPI3K/Akt/NF-κB signaling pathway

Identifiers

PMID25120775
PMCPMC4129010
OpenAlexW94514866

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.