Evidence map›Paper›PMID 25504228›Full record

ReviewProceedings of the Japan Academy. Series B, Physical and biological sciences2014

The molecular basis of myeloid malignancies.

Toshio Kitamura, Daichi Inoue, Naoko Okochi-Watanabe, Naoko Kato, Yukiko Komeno, Yang Lu, Yutaka Enomoto, Noriko Doki, Tomoyuki Uchida, Yuki Kagiyama and 11 more

Open access · diamondAbstract readReview
In one paragraph

Review in Proceedings of the Japan Academy. Series B, Physical and biological sciences, 2014. 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
1.7field-weighted citation impact, top 15% 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, 23 citations in OpenAlex.

  1. Review
  2. Impact of single versus multiple spliceosome mutations on myelodysplastic syndrome.Journal of clinical and experimental hematopathology : JCEH · 2023
    Article
  3. Review
  4. Article
  5. Article
  6. RAF Kinase Inhibitor Protein in Myeloid Leukemogenesis.International journal of molecular sciences · 2019
    Review
  7. Article
  8. BET-ting on Nrf2: How Nrf2 Signaling can Influence the Therapeutic Activities of BET Protein Inhibitors.BioEssays : news and reviews in molecular, cellular and developmental biology · 2018
    Review
  9. Review
  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

21 authors at 1 institution in 1 country.

Toshio KitamuraDivision of Cellular Therapy/Division of Stem Cell Signaling, The Institute of Medical Science, The University of Tokyo.
Daichi Inoue
Naoko Okochi-Watanabe
Naoko Kato
Yukiko Komeno
Yang Lu
Yutaka Enomoto
Noriko Doki
Tomoyuki Uchida
Yuki Kagiyama
Katsuhiro Togami
Kimihito C Kawabata
Reina Nagase
Sayuri Horikawa
Yasutaka Hayashi
Makoto Saika
Tomofusa Fukuyama
Kumi Izawa
Toshihiko Oki
Fumio Nakahara
Jiro Kitaura
The University of Tokyo · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Myeloid malignancies consist of acute myeloid leukemia (AML), myelodysplastic syndromes (MDS) and myeloproliferative neoplasm (MPN). The latter two diseases have preleukemic features and frequently evolve to AML. As with solid tumors, multiple mutations are required for leukemogenesis. A decade ago, these gene alterations were subdivided into two categories: class I mutations stimulating cell growth or inhibiting apoptosis; and class II mutations that hamper differentiation of hematopoietic cells. In mouse models, class I mutations such as the Bcr-Abl fusion kinase induce MPN by themselves and some class II mutations such as Runx1 mutations induce MDS. Combinations of class I and class II mutations induce AML in a variety of mouse models. Thus, it was postulated that hematopoietic cells whose differentiation is blocked by class II mutations would autonomously proliferate with class I mutations leading to the development of leukemia. Recent progress in high-speed sequencing has enabled efficient identification of novel mutations in a variety of molecules including epigenetic factors, splicing factors, signaling molecules and proteins in the cohesin complex; most of these are not categorized as either class I or class II mutations. The functional consequences of these mutations are now being extensively investigated. In this article, we will review the molecular basis of hematological malignancies, focusing on mouse models and the interfaces between these models and clinical findings, and revisit the classical class I/II hypothesis.

Indexed as

Epigenesis, GeneticMutationAnimalsCell ProliferationCell Transformation, NeoplasticFusion Proteins, bcr-ablHematologic NeoplasmsHumansLeukemia, Myeloid, AcuteMiceMyelodysplastic SyndromesFusion Proteins, bcr-abl

Identifiers

PMID25504228
PMCPMC4335136
OpenAlexW2019524792

What OpenQuestion holds

Textmetadata
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.