Evidence map›Paper›PMID 27270502›Full record

ArticleInternational journal of cancer2016

Kif14 overexpression accelerates murine retinoblastoma development.

Michael O'Hare, Mehdi Shadmand, Rania S Sulaiman, Kamakshi Sishtla, Toshiaki Sakisaka, Timothy W Corson

Open access · greenAbstract read
In one paragraph

Article in International journal of cancer, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed, 20 citations in OpenAlex.

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  10. Retinoblastoma, the visible CNS tumor: A review.Journal of neuroscience research · 2019
    Review
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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

6 authors at 5 institutions in 4 countries.

Michael O'HareEugene and Marilyn Glick Eye Institute, Indiana University School of Medicine, Indianapolis, IN.
Mehdi ShadmandEugene and Marilyn Glick Eye Institute, Indiana University School of Medicine, Indianapolis, IN.
Rania S SulaimanEugene and Marilyn Glick Eye Institute, Indiana University School of Medicine, Indianapolis, IN.
Kamakshi SishtlaEugene and Marilyn Glick Eye Institute, Indiana University School of Medicine, Indianapolis, IN.
Toshiaki SakisakaDivision of Membrane Dynamics, Department of Physiology and Cell Biology, Kobe University Graduate School of Medicine, Kobe, Hyogo, Japan.
Timothy W CorsonEugene and Marilyn Glick Eye Institute, Indiana University School of Medicine, Indianapolis, IN.ORCID 0000-0002-1402-7875
Midwest Eye Institute · USCairo University · EGIndiana University Health · USKobe University · JPUniversity of Ulster · GB

Funding

Indiana Clinical and Translational Sciences InstituteUL1TR001108 · NCATS · INDIANA UNIVERSITY INDIANAPOLIS · PI DENNE, SCOTT C., SHEKHAR, ANANTHA · 2013 to 2017
$23.3M
Indiana Clinical and Translational Sciences InstituteKL2TR001106 · NCATS · INDIANA UNIVERSITY INDIANAPOLIS · PI DENNE, SCOTT C., SHEKHAR, ANANTHA · 2013 to 2017
$3.2M
NCATS NIH HHS KL2 TR001106NCATS NIH HHS UL1 TR001108
6 · The paper itself

Abstract

The mitotic kinesin KIF14 has an essential role in the recruitment of proteins required for the final stages of cytokinesis. Genomic gain and/or overexpression of KIF14 has been documented in retinoblastoma and a number of other cancers, such as breast, lung and ovarian carcinomas, strongly suggesting its role as an oncogene. Despite evidence of oncogenic properties in vitro and in xenografts, Kif14's role in tumor progression has not previously been studied in a transgenic cancer model. Using a novel Kif14 overexpressing, simian virus 40 large T-antigen retinoblastoma (TAg-RB) double transgenic mouse model, we aimed to determine Kif14's role in promoting retinal tumor formation. Tumor initiation and development in double transgenics and control TAg-RB littermates were documented in vivo over a time course by optical coherence tomography, with subsequent ex vivo quantification of tumor burden. Kif14 overexpression led to an accelerated initiation of tumor formation in the TAg-RB model and a significantly decreased tumor doubling time (1.8 vs. 2.9 weeks). Moreover, overall percentage tumor burden was also increased by Kif14 overexpression. These data provide the first evidence that Kif14 can promote tumor formation in susceptible cells in vivo.

Indexed as

AnimalsAntigens, Viral, TumorCell Growth ProcessesDisease Models, AnimalFemaleKinesinsMaleMiceMice, Inbred C57BLMice, TransgenicRetinal NeoplasmsRetinoblastomaSimian virus 40Antigens, Viral, TumorKif14 protein, mouseKinesinskinesinoncogeneoptical coherence tomographyretinoblastomatransgenic mouse

Identifiers

PMID27270502
PMCPMC4980179
OpenAlexW2415573452

What OpenQuestion holds

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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.