Evidence map›Paper›PMID 28938528›Full record

ArticleOncotarget2017

p53-independent p21 induction by MELK inhibition.

Tatsuo Matsuda, Taigo Kato, Kazuma Kiyotani, Yunus Emre Tarhan, Vassiliki Saloura, Suyoun Chung, Koji Ueda, Yusuke Nakamura, Jae-Hyun Park

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 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

36 citing papers in PubMed, 50 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 3 institutions in 2 countries.

Tatsuo MatsudaDepartment of Medicine, The University of Chicago, Chicago, IL, USA.
Taigo KatoDepartment of Medicine, The University of Chicago, Chicago, IL, USA.
Kazuma KiyotaniDepartment of Medicine, The University of Chicago, Chicago, IL, USA.
Yunus Emre TarhanDepartment of Medicine, The University of Chicago, Chicago, IL, USA.
Vassiliki SalouraDepartment of Medicine, The University of Chicago, Chicago, IL, USA.
Suyoun ChungOncoTherapy Science Inc., Kawasaki, Japan.
Koji UedaProject for Realization of Personalized Cancer Medicine, Cancer Precision Medicine Center, Japanese Foundation for Cancer Research, Tokyo, Japan.
Yusuke NakamuraDepartment of Medicine, The University of Chicago, Chicago, IL, USA.
Jae-Hyun ParkDepartment of Medicine, The University of Chicago, Chicago, IL, USA.
University of Chicago · USJapanese Foundation For Cancer Research · JPOncoTherapy Science (Japan) · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MELK play critical roles in human carcinogenesis through activation of cell proliferation, inhibition of apoptosis and maintenance of stemness. Therefore, MELK is a promising therapeutic target for a wide range of cancers. Although p21 is a well-known p53-downstream gene, we found that treatment with a potent MELK inhibitor, OTS167, could induce p21 protein expression in cancer cell lines harboring loss-of-function

Indexed as

FoxO familymaternal embryonic leucine zipper kinasemolecular targetp21p53

Identifiers

PMID28938528
PMCPMC5601624
OpenAlexW2625741190

What OpenQuestion holds

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LicenceCC BY
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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.