Evidence map›Paper›PMID 34012401›Full record

ArticleFrontiers in pharmacology2021

Novel Pan-Pim Kinase Inhibitors With Imidazopyridazine and Thiazolidinedione Structure Exert Potent Antitumor Activities.

Yuichi Sawaguchi, Ryuta Yamazaki, Yukiko Nishiyama, Masayuki Mae, Atsuhiro Abe, Hiroyuki Nishiyama, Fukiko Nishisaka, Tatsuya Ibuki, Toshio Sasai, Takeshi Matsuzaki

Open access · goldAbstract read
In one paragraph

Article in Frontiers in pharmacology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

10 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. Review
  3. UM171 suppresses breast cancer progression by inducing KLF2.Breast cancer research and treatment · 2024
    Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Biological Therapies in the Treatment of Cancer-Update and New Directions.International journal of molecular sciences · 2021
    Review
  9. Article
  10. 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

10 authors at 2 institutions in 1 country.

Yuichi SawaguchiYakult Central Institute, Yakult Honsha Co. Ltd., Tokyo, Japan.
Ryuta YamazakiYakult Central Institute, Yakult Honsha Co. Ltd., Tokyo, Japan.
Yukiko NishiyamaYakult Central Institute, Yakult Honsha Co. Ltd., Tokyo, Japan.
Masayuki MaeYakult Central Institute, Yakult Honsha Co. Ltd., Tokyo, Japan.
Atsuhiro AbeYakult Central Institute, Yakult Honsha Co. Ltd., Tokyo, Japan.
Hiroyuki NishiyamaYakult Central Institute, Yakult Honsha Co. Ltd., Tokyo, Japan.
Fukiko NishisakaYakult Central Institute, Yakult Honsha Co. Ltd., Tokyo, Japan.
Tatsuya IbukiYakult Central Institute, Yakult Honsha Co. Ltd., Tokyo, Japan.
Toshio SasaiYakult Central Institute, Yakult Honsha Co. Ltd., Tokyo, Japan.
Takeshi MatsuzakiYakult Central Institute, Yakult Honsha Co. Ltd., Tokyo, Japan.
Yakult Central Institute · JPYakult Honsha (Japan) · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pim kinases are overexpressed in various types of hematological malignancies and solid carcinomas, and promote cell proliferation and survival. Here in this study, we investigated the preclinical profile of novel pan-Pim kinase inhibitors with imidazopyridazine and thiazolidinedione structure. Imidazopyridazine-thiazolidinediones inhibited activities of Pim kinases with IC

Indexed as

anticancer drugimidazopyridazinepan-pim kinase inhibitorpim kinasetargeted therapythiazolidinedione

Identifiers

PMID34012401
PMCPMC8126654
OpenAlexW3157372933

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.