Evidence map›Paper›PMID 30076184›Full record

ArticleHaematologica2018

Cyclin-dependent kinase 9 as a potential specific molecular target in NK-cell leukemia/lymphoma.

Shiori Kinoshita, Takashi Ishida, Asahi Ito, Tomoko Narita, Ayako Masaki, Susumu Suzuki, Takashi Yoshida, Masaki Ri, Shigeru Kusumoto, Hirokazu Komatsu and 7 more

Abstract read
In one paragraph

Article in Haematologica, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Review
  5. CDK9 inhibitors in cancer research.RSC medicinal chemistry · 2022
    Review
  6. Article
  7. Article
  8. Adaptive responses toProceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  9. Review
  10. P-TEFb as A Promising Therapeutic Target.Molecules (Basel, Switzerland) · 2020
    Review
  11. Article
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

17 authors.

Shiori KinoshitaDepartment of Hematology and Oncology, Nagoya City University Graduate School of Medical Sciences, Japan.
Takashi IshidaDepartment of Hematology and Oncology, Nagoya City University Graduate School of Medical Sciences, Japan itakashi@iwate-med.ac.jp.
Asahi ItoDepartment of Hematology and Oncology, Nagoya City University Graduate School of Medical Sciences, Japan.
Tomoko NaritaDepartment of Hematology and Oncology, Nagoya City University Graduate School of Medical Sciences, Japan.
Ayako MasakiDepartment of Hematology and Oncology, Nagoya City University Graduate School of Medical Sciences, Japan.
Susumu SuzukiDepartment of Tumor Immunology, Aichi Medical University School of Medicine, Japan.
Takashi YoshidaDepartment of Hematology and Oncology, Nagoya City University Graduate School of Medical Sciences, Japan.
Masaki RiDepartment of Hematology and Oncology, Nagoya City University Graduate School of Medical Sciences, Japan.
Shigeru KusumotoDepartment of Hematology and Oncology, Nagoya City University Graduate School of Medical Sciences, Japan.
Hirokazu KomatsuDepartment of Hematology and Oncology, Nagoya City University Graduate School of Medical Sciences, Japan.
Norio ShimizuDepartment of Virology, Division of Medical Science, Medical Research Institute, Tokyo Medical and Dental University, Japan.
Hiroshi InagakiDepartment of Pathology and Molecular Diagnostics, Nagoya City University Graduate School of Medical Sciences, Japan.
Taruho KurodaBayer Yakuhin, Ltd., Osaka, Japan.
Arne ScholzBayer AG Pharmaceuticals Division, Berlin, Germany.
Ryuzo UedaDepartment of Tumor Immunology, Aichi Medical University School of Medicine, Japan.
Takaomi SandaCancer Science Institute of Singapore, National University of Singapore.
Shinsuke IidaDepartment of Hematology and Oncology, Nagoya City University Graduate School of Medical Sciences, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BAY 1143572 is a highly selective inhibitor of cyclin-dependent kinase 9/positive transcription elongation factor b. It has entered phase I clinical studies. Here, we have assessed the utility of BAY 1143572 for treating natural killer (NK) cell leukemias/lymphomas that have a poor prognosis, namely extranodal NK/T-cell lymphoma, nasal type and aggressive NK-cell leukemia, in a preclinical mouse model in vivo as well as in tissue culture models

Indexed as

AnimalsAntineoplastic AgentsCell Line, TumorCell ProliferationCyclin-Dependent Kinase 9HumansKaplan-Meier EstimateKiller Cells, NaturalLeukemiaLymphomaMice, Inbred NODMice, KnockoutMice, SCIDMolecular Targeted TherapySulfonamidesTriazinesAntineoplastic AgentsatuveciclibCyclin-Dependent Kinase 9SulfonamidesTriazines

Identifiers

PMID30076184
PMCPMC6269314

What OpenQuestion holds

Textmetadata
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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.