Evidence map›Paper›PMID 31186254›Full record

ReviewBlood advances2019

The role of aurora A and polo-like kinases in high-risk lymphomas.

Carlos Murga-Zamalloa, Kedar V Inamdar, Ryan A Wilcox

Open access · goldAbstract readReview
In one paragraph

Review in Blood advances, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

17 citing papers in PubMed, 25 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

3 authors at 2 institutions in 1 country.

Carlos Murga-ZamalloaDivision of Hematology-Oncology, Department of Internal Medicine, University of Michigan, Ann Arbor, MI; and.
Kedar V InamdarDepartment of Pathology, Henry Ford Hospital, Detroit, MI.
Ryan A WilcoxDivision of Hematology-Oncology, Department of Internal Medicine, University of Michigan, Ann Arbor, MI; and.
University of Michigan–Ann Arbor · USHenry Ford Hospital · US

Funding

TXNIP as a Key Regulator of Thyroid Cancer Metabolism and AggressivenessR01CA175994 · NCI · UNIVERSITY OF COLORADO DENVER · PI HAUGEN, BRYAN R. · 2013 to 2017
$1.6M
Wiskott-Aldrich syndrome protein (WASp) signaling in the oncogenesis of T celllymphomasK08CA218460 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MURGA-ZAMALLOA, CARLOS A. · 2017 to 2019
$320k
NCI NIH HHS K08 CA218460NCI NIH HHS R01 CA175994
6 · The paper itself

Abstract

High-risk lymphomas (HRLs) are associated with dismal outcomes and remain a therapeutic challenge. Recurrent genetic and molecular alterations, including c-myc expression and aurora A kinase (AAK) and polo-like kinase-1 (PLK1) activation, promote cell proliferation and contribute to the highly aggressive natural history associated with these lymphoproliferative disorders. In addition to its canonical targets regulating mitosis, the AAK/PLK1 axis directly regulates noncanonical targets, including c-myc. Recent studies demonstrate that HRLs, including T-cell lymphomas and many highly aggressive B-cell lymphomas, are dependent upon the AAK/PLK1 axis. Therefore, the AAK/PLK1 axis has emerged as an attractive therapeutic target in these lymphomas. In addition to reviewing these recent findings, we summarize the rationale for targeting AAK/PLK1 in high-risk and c-myc-driven lymphoproliferative disorders.

Indexed as

Signal TransductionAnimalsAurora Kinase ACell Cycle ProteinsHumansLymphoma, B-CellLymphoma, T-CellPolo-Like Kinase 1Protein Serine-Threonine KinasesProto-Oncogene ProteinsProto-Oncogene Proteins c-mycRisk FactorsAURKA protein, humanAurora Kinase ACell Cycle ProteinsMYC protein, humanPolo-Like Kinase 1Protein Serine-Threonine KinasesProto-Oncogene ProteinsProto-Oncogene Proteins c-myc

Identifiers

PMID31186254
PMCPMC6560346
OpenAlexW2952763999

What OpenQuestion holds

Textmetadata
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.