Evidence map›Paper›PMID 28245563›Full record

ArticleInternational journal of molecular sciences2017

NANOG Expression as a Responsive Biomarker during Treatment with Hedgehog Signal Inhibitor in Acute Myeloid Leukemia.

Seiji Kakiuchi, Yosuke Minami, Yoshiharu Miyata, Yu Mizutani, Hideaki Goto, Shinichiro Kawamoto, Kimikazu Yakushijin, Keiji Kurata, Hiroshi Matsuoka, Hironobu Minami

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

14 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Tumor heterogeneity and resistance in glioblastoma: the role of stem cells.Apoptosis : an international journal on programmed cell death · 2025
    Review
  3. Review
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  10. The Role of Hedgehog Pathway in Female Cancers.Journal of cancer science and clinical therapeutics · 2020
    Article
  11. Review
  12. Review
  13. 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

10 authors at 2 institutions in 1 country.

Seiji KakiuchiDepartment of Medical Oncology and Hematology, Kobe University Graduate School of Medicine, Kobe 650-0017, Japan. kakiuchi@med.kobe-u.ac.jp.
Yosuke MinamiDepartment of Transfusion Medicine and Cell Therapy, Kobe University Hospital, Kobe 650-0017, Japan. minamiy@med.kobe-u.ac.jp.
Yoshiharu MiyataDepartment of Medical Oncology and Hematology, Kobe University Graduate School of Medicine, Kobe 650-0017, Japan. yhmiyata@med.kobe-u.ac.jp.
Yu MizutaniDepartment of Medical Oncology and Hematology, Kobe University Graduate School of Medicine, Kobe 650-0017, Japan. mizuyu@med.kobe-u.ac.jp.
Hideaki GotoDepartment of Medical Oncology and Hematology, Kobe University Graduate School of Medicine, Kobe 650-0017, Japan. hgoto@med.kobe-u.ac.jp.
Shinichiro KawamotoDepartment of Medical Oncology and Hematology, Kobe University Hospital, Kobe 650-0017, Japan. skawamo@med.kobe-u.ac.jp.
Kimikazu YakushijinDepartment of Medical Oncology and Hematology, Kobe University Hospital, Kobe 650-0017, Japan. kyakushi@med.kobe-u.ac.jp.
Keiji KurataDepartment of Medical Oncology and Hematology, Kobe University Graduate School of Medicine, Kobe 650-0017, Japan. kkurata@med.kobe-u.ac.jp.
Hiroshi MatsuokaDepartment of Medical Oncology and Hematology, Kobe University Graduate School of Medicine, Kobe 650-0017, Japan. matsuoh@med.kobe-u.ac.jp.
Hironobu MinamiDepartment of Medical Oncology and Hematology, Kobe University Graduate School of Medicine, Kobe 650-0017, Japan. hminami@med.kobe-u.ac.jp.
Kobe University · JPKobe University Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aberrant activation of the Hedgehog (Hh) signaling pathway is involved in the maintenance of leukemic stem cell (LSCs) populations. PF-0444913 (PF-913) is a novel inhibitor that selectively targets Smoothened (SMO), which regulates the Hh pathway. Treatment with PF-913 has shown promising results in an early phase study of acute myeloid leukemia (AML). However, a detailed mode of action for PF-913 and relevant biomarkers remain to be elucidated. In this study, we examined bone marrow samples derived from AML patients under PF-913 monotherapy. Gene set enrichment analysis (GSEA) revealed that PF-913 treatment affected the self-renewal signature and cell-cycle regulation associated with LSC-like properties. We then focused on the expression of a pluripotency factor, NANOG, because previous reports showed that a downstream effector in the Hh pathway, GLI, directly binds to the NANOG promoter and that the GLI-NANOG axis promotes stemness and growth in several cancers. In this study, we found that a change in NANOG transcripts was closely associated with GLI-target genes and NANOG transcripts can be a responsive biomarker during PF-913 therapy. Additionally, the treatment of AML with PF-913 holds promise, possibly through inducing quiescent leukemia stem cells toward cell cycling.

Indexed as

Antineoplastic AgentsBiomarkersCell CycleCell Line, TumorCell Self RenewalGene Expression ProfilingGene Expression Regulation, NeoplasticGene Knockdown TechniquesHedgehog ProteinsHumansLeukemia, Myeloid, AcuteNanog Homeobox ProteinNeoplastic Stem CellsSignal TransductionSmoothened ReceptorAntineoplastic AgentsBiomarkersHedgehog ProteinsNanog Homeobox ProteinSmoothened ReceptorSMO protein, humanacute myeloid leukemiabiomarkerhedgehog inhibitorNANOGself-renewal

Identifiers

PMID28245563
PMCPMC5372502
OpenAlexW2590271489

What OpenQuestion holds

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LicenceCC BY
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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.