Evidence map›Paper›PMID 27564113›Full record

ArticleOncotarget2017

Novel multiple tyrosine kinase inhibitor ponatinib inhibits bFGF-activated signaling in neuroblastoma cells and suppresses neuroblastoma growth in vivo.

Haoyu Li, Yongfeng Wang, Zhenghu Chen, Jiaxiong Lu, Jessie Pan, Yang Yu, Yanling Zhao, Huiyuan Zhang, Ting Hu, Qing Liu and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

16 citing papers in PubMed, 22 citations in OpenAlex.

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  9. A Combinatorial Strategy for TargetingClinical cancer research : an official journal of the American Association for Cancer Research · 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

11 authors at 3 institutions in 2 countries.

Haoyu LiDepartment of Neurosurgery, Xiangya Hospital, Central South University, Changsha 410008, China.
Yongfeng WangDepartment of Microbiology, Peking University Health Science Center, Beijing 100191, China.
Zhenghu ChenTexas Children's Cancer Center, Department of Pediatrics, Dan L. Duncan Cancer Center, Baylor College of Medicine, Houston, Texas 77030, USA.
Jiaxiong LuTexas Children's Cancer Center, Department of Pediatrics, Dan L. Duncan Cancer Center, Baylor College of Medicine, Houston, Texas 77030, USA.
Jessie PanTexas Children's Cancer Center, Department of Pediatrics, Dan L. Duncan Cancer Center, Baylor College of Medicine, Houston, Texas 77030, USA.
Yang YuTexas Children's Cancer Center, Department of Pediatrics, Dan L. Duncan Cancer Center, Baylor College of Medicine, Houston, Texas 77030, USA.
Yanling ZhaoTexas Children's Cancer Center, Department of Pediatrics, Dan L. Duncan Cancer Center, Baylor College of Medicine, Houston, Texas 77030, USA.
Huiyuan ZhangTexas Children's Cancer Center, Department of Pediatrics, Dan L. Duncan Cancer Center, Baylor College of Medicine, Houston, Texas 77030, USA.
Ting HuDepartment of Neurosurgery, Xiangya Hospital, Central South University, Changsha 410008, China.
Qing LiuDepartment of Neurosurgery, Xiangya Hospital, Central South University, Changsha 410008, China.
Jianhua YangTexas Children's Cancer Center, Department of Pediatrics, Dan L. Duncan Cancer Center, Baylor College of Medicine, Houston, Texas 77030, USA.
Baylor College of Medicine · USCentral South University · CNTongji University · CN

Funding

DUSP26: A Novel Therapeutic Target in NeuroblastomaR01NS072420 · NINDS · BAYLOR COLLEGE OF MEDICINE · PI YANG, JIANHUA · 2011 to 2014
$1.4M
TMEM108 IS A NOVEL TARGET IN NEUROBLASTOMAR21NS094654 · NINDS · BAYLOR COLLEGE OF MEDICINE · PI YANG, JIANHUA · 2016 to 2017
$436k
Targeting TAK1 in NeuroblastomaR21NS085467 · NINDS · BAYLOR COLLEGE OF MEDICINE · PI YANG, JIANHUA · 2013 to 2014
$430k
NINDS NIH HHS R01 NS072420NINDS NIH HHS R21 NS085467NINDS NIH HHS R21 NS094654
6 · The paper itself

Abstract

Neuroblastoma (NB) is one of the most common pediatric malignancies in children. Abnormal activation of receptor tyrosine kinases contributes to the pathological development of NB. Therefore, targeting tyrosine kinase receptors to cure NB is a promising strategy. Here, we report that a multi-targeted tyrosine kinase inhibitor ponatinib inhibited NB cell proliferation and induced NB cell apoptosis in a dose-dependent manner. In addition, ponatinib suppressed the colony formation ability of NB cells. Mechanistically, ponatinib effectively inhibited the FGFR1-activated signaling pathway. Ponatinib also enhanced the cytotoxic effects of doxorubicin on NB cells. Furthermore, ponatinib demonstrated anti-tumor efficacy in vivo by inhibiting tumor growth in an orthotopic xenograft NB mouse model. In summary, our results showed that ponatinib inhibited NB growth both in vitro and in vivo.

Indexed as

AnimalsCell Line, TumorCell ProliferationCell SurvivalDose-Response Relationship, DrugDoxycyclineDrug SynergismFibroblast Growth Factor 2Gene Expression Regulation, NeoplasticHumansImidazolesMiceNeuroblastomaProtein Kinase InhibitorsPyridazinesReceptor, Fibroblast Growth Factor, Type 1DoxycyclineFGFR1 protein, humanFibroblast Growth Factor 2ImidazolesponatinibProtein Kinase InhibitorsPyridazinesReceptor, Fibroblast Growth Factor, Type 1apoptosischemoresistanceFGFR1neuroblastomaponatinib

Identifiers

PMID27564113
PMCPMC5351597
OpenAlexW2516837092

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.