Evidence map›Paper›PMID 21980926›Full record

ReviewBritish journal of haematology2011

The potential role of Aurora kinase inhibitors in haematological malignancies.

Sherif S Farag

Open access · bronzeAbstract readReview
In one paragraph

Review in British journal of haematology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
3.4field-weighted citation impact, top 8% 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

33 citing papers in PubMed, 60 citations in OpenAlex.

  1. Trial
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  3. Phase II study of alisertib, a selective Aurora A kinase inhibitor, in relapsed and refractory aggressive B- and T-cell non-Hodgkin lymphomas.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2014
    Trial
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  5. Article
  6. Review
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  16. Review
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  18. Therapeutic Vulnerabilities inInternational journal of molecular sciences · 2018
    Article
  19. Article
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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

1 author at 1 institution in 1 country.

Sherif S FaragDivision of Hematology and Oncology, Department of Medicine, Indiana University School of Medicine, 840 Westr Walnut St., Indianapolis, IN 46202, USA. ssfarag@iupui.edu
Indiana University – Purdue University Indianapolis · US

Funding

Multiple kinase target inhibition with EMND-2076 in multiple myelomaR21CA141404 · NCI · INDIANA UNIVERSITY INDIANAPOLIS · PI FARAG, SHERIF S · 2010 to 2011
$630k
NCI NIH HHS CA141404NCI NIH HHS R21 CA141404
6 · The paper itself

Abstract

Aurora kinases play an important role in the control of the cell cycle and have been implicated in tumourigenesis in a number of cancers. Among the haematological malignancies, overexpression of Aurora kinases has been reported in acute myeloid leukaemia, chronic myeloid leukaemia, acute lymphoblastic leukaemia, multiple myeloma, aggressive non-Hodgkin lymphoma and Hodgkin lymphoma. A large number of Aurora kinase inhibitors are currently in different stages of clinical development. In addition to varying in their selectivity for the different Aurora kinases, some also have activity directed at other cellular kinases involved in important molecular pathways in cancer cells. This review summarizes the biology of Aurora kinases and discusses why they may be good therapeutic targets in different haematological cancers. We describe preclinical data that has served as the rationale for investigating Aurora kinase inhibitors in different haematological malignancies, and summarize published results from early phase clinical trials. While the anti-tumour effects of Aurora kinase inhibitors appear promising, we highlight important issues for future clinical research and suggest that the optimal use of these inhibitors is likely to be in combination with cytotoxic agents already in use for the treatment of various haematological cancers.

Indexed as

AnimalsAurora KinasesHematologic NeoplasmsHumansProtein Kinase InhibitorsProtein Serine-Threonine KinasesAurora KinasesProtein Kinase InhibitorsProtein Serine-Threonine Kinases

Identifiers

PMID21980926
PMCPMC3771583
OpenAlexW2012833528

What OpenQuestion holds

Textmetadata
LicenceTDM
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.