Evidence map›Paper›PMID 25491234›Full record

ReviewJournal of hematology & oncology2014

Pim kinases in hematological malignancies: where are we now and where are we going?

Patrizia Mondello, Salvatore Cuzzocrea, Michael Mian

Abstract readReview
In one paragraph

Review in Journal of hematology & oncology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
–field-weighted citation impact
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

52 citing papers in PubMed.

  1. Article
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  6. Review
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  8. Review
  9. The role of Pim-1 kinases in inflammatory signaling pathways.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2024
    Article
  10. Article
  11. Review
  12. Article
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  15. 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

3 authors.

Patrizia MondelloDepartment of Human Pathology, University of Messina, Via Consolare Valeria, 98125, Messina, Italy. patriziamondello@hotmail.it.
Salvatore CuzzocreaDepartment of Biological and Environmental Sciences, University of Messina, Messina, Italy. salvator@unime.it.
Michael MianDepartment of Hematology, Hospital S. Maurizio, Bolzano/Bozen, Italy. m.mian@webmaxxi.eu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The proviral insertion in murine (PIM) lymphoma proteins are a serine/threonine kinase family composed of three isoformes: Pim-1, Pim-2 and Pim-3. They play a critical role in the control of cell proliferation, survival, homing and migration. Recently, overexpression of Pim kinases has been reported in human tumors, mainly in hematologic malignancies. In vitro and in vivo studies have confirmed their oncogenic potential. Indeed, PIM kinases have shown to be involved in tumorgenesis, to enhance tumor growth and to induce chemo-resistance, which is why they have become an attractive therapeutic target for cancer therapy. Novel molecules inhibiting Pim kinases have been evaluated in preclinical studies, demonstrating to be effective and with a favorable toxicity profile. Given the promising results, some of these compounds are currently under investigation in clinical trials. Herein, we provide an overview of the biological activity of PIM-kinases, their role in hematologic malignancies and future therapeutic opportunities.

Indexed as

AnimalsHematologic NeoplasmsHumansMiceProtein Kinase InhibitorsProto-Oncogene Proteins c-pim-1Protein Kinase InhibitorsProto-Oncogene Proteins c-pim-1proto-oncogene proteins pim

Identifiers

PMID25491234
PMCPMC4266197

What OpenQuestion holds

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Registered trials

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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.