Evidence map›Paper›PMID 26583567›Full record

ArticleCancer science2016

Novel oral transforming growth factor-β signaling inhibitor EW-7197 eradicates CML-initiating cells.

Kazuhito Naka, Kaori Ishihara, Yoshie Jomen, Cheng Hua Jin, Dong-Hyun Kim, Yoon-Kang Gu, Eun-Sook Jeong, Shaoguang Li, Daniela S Krause, Dong-Wook Kim and 9 more

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

18 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Vactosertib potently improves anti-tumor properties of 5-FU for colon cancer.Daru : journal of Faculty of Pharmacy, Tehran University of Medical Sciences · 2023
    Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. The Role of TGF-Evidence-based complementary and alternative medicine : eCAM · 2021
    Review
  9. Article
  10. Review
  11. Article
  12. Review
  13. Targeting TGF-β Signaling for Therapeutic Gain.Cold Spring Harbor perspectives in biology · 2017
    Review
  14. Review
  15. Review
  16. Article
  17. Article
  18. 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

19 authors at 5 institutions in 4 countries.

Kazuhito NakaExploratory Project on Cancer Stem Cells, Cancer Research Institute, Kanazawa University, Kanazawa, Japan.
Kaori IshiharaExploratory Project on Cancer Stem Cells, Cancer Research Institute, Kanazawa University, Kanazawa, Japan.
Yoshie JomenExploratory Project on Cancer Stem Cells, Cancer Research Institute, Kanazawa University, Kanazawa, Japan.
Cheng Hua JinGraduate School of Pharmaceutical Sciences, College of Pharmacy, Ewha Womans University, Seoul, Korea.
Dong-Hyun KimDepartment of Pharmacology and PharmacoGenomics Research Center, Inje University College of Medicine, Busan, Korea.
Yoon-Kang GuDepartment of Pharmacology and PharmacoGenomics Research Center, Inje University College of Medicine, Busan, Korea.
Eun-Sook JeongDepartment of Pharmacology and PharmacoGenomics Research Center, Inje University College of Medicine, Busan, Korea.
Shaoguang LiDivision of Hematology/Oncology, Department of Medicine, University of Massachusetts Medical School, Worcester, Massachusetts, USA.
Daniela S KrauseInstitute for Tumor Biology and Experimental Therapy, Georg Speyer Haus, Goethe University, Frankfurt, Germany.
Dong-Wook KimDepartment of Hematology, Seoul St. Mary's Hospital, Cancer Research Institute, The Catholic University of Korea, Seoul, Korea.
Eunjin BaeExploratory Project on Cancer Stem Cells, Cancer Research Institute, Kanazawa University, Kanazawa, Japan.
Yoshihiro TakiharaDepartment of Stem Cell Biology, Research Institute for Radiation Biology and Medicine, Hiroshima University, Hiroshima, Japan.
Atsushi HiraoDivision of Molecular Genetics, Cancer Research Institute, Kanazawa University, Kanazawa, Japan.
Hiroko OshimaDivision of Genetics, Cancer Research Institute, Kanazawa University, Kanazawa, Japan.
Masanobu OshimaDivision of Genetics, Cancer Research Institute, Kanazawa University, Kanazawa, Japan.
Akira OoshimaCHA Cancer Institute and Department of Biomedical Science, CHA University, Seongnam, Korea.
Yhun Yhong SheenCollege of Pharmacy, Ewha Womans University, Seoul, Korea.
Seong-Jin KimCHA Cancer Institute and Department of Biomedical Science, CHA University, Seongnam, Korea.
Dae-Kee KimGraduate School of Pharmaceutical Sciences, College of Pharmacy, Ewha Womans University, Seoul, Korea.
Kanazawa University · JPInje University · KRCHA University · KREwha Womans University · KRGoethe University Frankfurt · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent strategies for treating CML patients have focused on investigating new combinations of tyrosine kinase inhibitors (TKIs) as well as identifying novel translational research agents that can eradicate CML leukemia-initiating cells (CML-LICs). However, little is known about the therapeutic benefits such CML-LIC targeting therapies might bring to CML patients. In this study, we investigated the therapeutic potential of EW-7197, an orally bioavailable transforming growth factor-β signaling inhibitor which has recently been approved as an Investigational New Drug (NIH, USA), to suppress CML-LICs in vivo. Compared to TKI treatment alone, administration of TKI plus EW-7197 to CML-affected mice significantly delayed disease relapse and prolonged survival. Notably, combined treatment with EW-7197 plus TKI was effective in eliminating CML-LICs even if they expressed the TKI-resistant T315I mutant BCR-ABL1 oncogene. Collectively, these results indicate that EW-7197 may be a promising candidate for a new therapeutic that can greatly benefit CML patients by working in combination with TKIs to eradicate CML-LICs.

Indexed as

Aniline CompoundsAnimalsAntineoplastic Combined Chemotherapy ProtocolsCell ProliferationDisease Models, AnimalHumansImidazolesLeukemia, Myelogenous, Chronic, BCR-ABL PositiveMiceMice, Inbred C57BLProtein Kinase InhibitorsProtein Serine-Threonine KinasesPyridazinesReceptors, Transforming Growth Factor betaReceptor, Transforming Growth Factor-beta Type ITransfectionAniline CompoundsImidazolesponatinibProtein Kinase InhibitorsProtein Serine-Threonine KinasesPyridazinesReceptors, Transforming Growth Factor betaReceptor, Transforming Growth Factor-beta Type ITGFBR1 protein, humanTgfbr1 protein, mouseTransforming Growth Factor betaTriazolesvactosertibALK5 inhibitorCML stem cellsrelapse preventionTGF-β signalingTKI resistance

Identifiers

PMID26583567
PMCPMC4768399
OpenAlexW2172546656

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.