Evidence map›Paper›PMID 28592839›Full record

ArticleScientific reports2017

Inhibition of AURKA kinase activity suppresses collective invasion in a microfluidic cell culture platform.

Jiang-Long Xia, Wen-Jun Fan, Fei-Meng Zheng, Wen-Wen Zhang, Jia-Jun Xie, Meng-Ying Yang, Muhammad Kamran, Peng Wang, Hong-Ming Teng, Chun-Li Wang and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.4field-weighted citation impact, top 41% 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

9 citing papers in PubMed, 18 citations in OpenAlex.

  1. Microphysiological systems for metastasis research: a stepwise approach.Cellular oncology (Dordrecht, Netherlands) · 2025
    Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
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  8. The role of Aurora-A in human cancers and future therapeutics.American journal of cancer research · 2020
    Review
  9. Article
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 5 institutions in 1 country.

Jiang-Long XiaInstitute of Cancer Stem Cell, Dalian Medical University, Dalian, China.
Wen-Jun FanInstitute of Cancer Stem Cell, Dalian Medical University, Dalian, China.
Fei-Meng ZhengDepartment of Medical Oncology, The Eastern Hospital of The First Affiliated Hospital, Sun Yat-Sen University, Guangzhou, China.
Wen-Wen ZhangDepartment of Oncology, The First Hospital Affiliated to Dalian Medical University, Dalian, China.
Jia-Jun XieDepartment of Hematology, The Second Affiliated Hospital of Dalian Medical University, Dalian, China.
Meng-Ying YangInstitute of Cancer Stem Cell, Dalian Medical University, Dalian, China.
Muhammad KamranInstitute of Cancer Stem Cell, Dalian Medical University, Dalian, China.
Peng WangDepartment of Thoracic Surgery, The First Hospital Affiliated to Dalian Medical University, Dalian, China.
Hong-Ming TengInstitute of Cancer Stem Cell, Dalian Medical University, Dalian, China.
Chun-Li WangInstitute of Cancer Stem Cell, Dalian Medical University, Dalian, China.
Quentin LiuInstitute of Cancer Stem Cell, Dalian Medical University, Dalian, China. liuq9@mail.sysu.edu.cn.
Dalian Medical University · CNFirst Affiliated Hospital of Dalian Medical University · CNSun Yat-sen University Cancer Center · CNThe First Affiliated Hospital, Sun Yat-sen University · CNThird Affiliated Hospital of Sun Yat-sen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumor local invasion is the first step of metastasis cascade which remains the key obstacle for cancer therapy. Collective cell migration plays a critical role in tumor invading into surrounding tissues. In vitro assays fail to assess collective invasion in a real time manner. Herein we aim to develop a three-dimensional (3D) microfluidic cell invasion model to determine the dynamic process. In this model, collective invasion of breast cancer cells is induced by the concentration gradient of fetal bovine serum. We find that breast cancer cells adopt a collective movement rather than a random manner when the cells invade into extracellular matrix. The leading cells in the collective movement exhibit an increased expression of an Aurora kinase family protein - AURKA compared with the follower cells. Inhibition of AURKA kinase activity by VX680 or AKI603 significantly reduces the phosphorylation of ERK1/2 (Thr202/Tyr204) and collective cohort formation. Together, our study illustrates that AURKA acts as a potential therapeutic target for suppressing the process of tumor collective invasion. The 3D microfluidic cell invasion model is a reliable, measurable and dynamic platform for exploring potential drugs to inhibit tumor collective invasion.

Indexed as

MicrofluidicsAurora Kinase ACell Culture TechniquesCell Line, TumorCell MovementExtracellular Signal-Regulated MAP KinasesFluorescent Antibody TechniqueGene ExpressionHumansProtein Kinase InhibitorsAurora Kinase AExtracellular Signal-Regulated MAP KinasesProtein Kinase Inhibitors

Identifiers

PMID28592839
PMCPMC5462816
OpenAlexW2621098992

What OpenQuestion holds

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LicenceCC BY
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.