Evidence map›Paper›PMID 25720956›Full record

ArticleScientific reports2015

The multi-targeted tyrosine kinase inhibitor vandetanib plays a bifunctional role in non-small cell lung cancer cells.

Yan Zhou, Yuanliang Zhang, Hanbing Zou, Ning Cai, Xiaojing Chen, Longmei Xu, Xianming Kong, Peifeng Liu

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. 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
1.3field-weighted citation impact, top 21% 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, 25 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Selective Killing of Cancer Cells by Nonplanar Aromatic Hydrocarbon-Induced DNA Damage.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2019
    Article
  10. Article
  11. Discovery of Pyrido[3',2':5,6]thiopyrano[4,3-ACS medicinal chemistry letters · 2019
    Article
  12. Article
  13. Review
  14. 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

8 authors at 2 institutions in 1 country.

Yan ZhouCentral Laboratory, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai. 200127, People's Republic of China.
Yuanliang ZhangShanghai Institute of Hematology, Ruijin Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai. 200025, People's Republic of China.
Hanbing ZouCentral Laboratory, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai. 200127, People's Republic of China.
Ning CaiCentral Laboratory, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai. 200127, People's Republic of China.
Xiaojing ChenCentral Laboratory, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai. 200127, People's Republic of China.
Longmei XuCentral Laboratory, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai. 200127, People's Republic of China.
Xianming Kong1] Central Laboratory, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai. 200127, People's Republic of China [2] State Key Laboratory of Oncogenes and Related Genes, Shanghai Cancer Institute, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai. 200032, People's Republic of China.
Peifeng Liu1] Central Laboratory, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai. 200127, People's Republic of China [2] State Key Laboratory of Oncogenes and Related Genes, Shanghai Cancer Institute, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai. 200032, People's Republic of China.
Shanghai Jiao Tong University · CNShanghai Institute of Hematology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Vandetanib, a multikinase inhibitor, is a target of drug treatments for non-small cell lung cancer (NSCLC). However, phase II and III clinical trials have not conclusively demonstrated the curative effects of vandetanib for NSCLC, and the reasons for this are unknown. In the present study, we use the NSCLC cell line Calu-6 as a model to determine the cellular and biological effects of vandetanib. Our results demonstrate that vandetanib impairs Calu-6 cell migration and invasion. We find that vandetanib can directly inhibit RET activity, which influences the Rho-JNK pathway. Overexpression of a constitutively active Rho GTPase antagonizes the inhibitory effects of vandetanib on Calu-6 cells invasion and JNK pathway activation. In addition, vandetanib induces autophagy by increasing the level of reactive oxygen species (ROS) in Calu-6 cells, and blockade of autophagy or ROS effectively enhances the cell death effect of vandetanib. In this study, we find vandetanib is of a double effect in some NSCLC cells, presenting new possibilities for the pharmacological treatment of NSCLC and introducing a novel role for vandetanib in treatment options.

Indexed as

Actin CytoskeletonAntineoplastic AgentsCarcinoma, Non-Small-Cell LungCell Line, TumorCell MovementCell ShapeCell SurvivalDrug Screening Assays, AntitumorHumansLung NeoplasmsMAP Kinase Signaling SystemPiperidinesProtein Kinase InhibitorsQuinazolinesReactive Oxygen Speciesrho GTP-Binding ProteinsAntineoplastic AgentsPiperidinesProtein Kinase InhibitorsQuinazolinesReactive Oxygen Speciesrho GTP-Binding Proteinsvandetanib

Identifiers

PMID25720956
PMCPMC4342569
OpenAlexW2021738367

What OpenQuestion holds

Textmetadata
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.