Evidence map›Paper›PMID 27634205›Full record

ArticleHaematologica2017

ZNF384-related fusion genes define a subgroup of childhood B-cell precursor acute lymphoblastic leukemia with a characteristic immunotype.

Shinsuke Hirabayashi, Kentaro Ohki, Kazuhiko Nakabayashi, Hitoshi Ichikawa, Yukihide Momozawa, Kohji Okamura, Akinori Yaguchi, Kazuki Terada, Yuya Saito, Ai Yoshimi and 30 more

Open access · goldAbstract read
In one paragraph

Article in Haematologica, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 130 papers.

0numbers the graph read from it
0cells of the map it votes in
130citing papers in PubMed
12.4field-weighted citation impact, top 1% 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

130 citing papers in PubMed, 237 citations in OpenAlex.

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70 more citing papers are in PubMed but not listed here.

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

40 authors at 20 institutions in 1 country.

Shinsuke HirabayashiDepartment of Pediatric Hematology and Oncology Research, National Research Institute for Child Health and Development, Setagaya-ku, Tokyo, Japan.
Kentaro OhkiDepartment of Pediatric Hematology and Oncology Research, National Research Institute for Child Health and Development, Setagaya-ku, Tokyo, Japan kiyokawa-n@ncchd.go.jp oki-kn@ncchd.go.jp.
Kazuhiko NakabayashiDepartment of Maternal-Fetal Biology, National Research Institute for Child Health and Development, Setagaya-ku, Tokyo, Japan.
Hitoshi IchikawaDivision of Genetics, National Cancer Center Research Institute, Chuo-ku, Tokyo, Japan.
Yukihide MomozawaLaboratory for Genotyping Development, Center for Integrative Medical Sciences (IMS), RIKEN, Yokohama-shi, Kanagawa, Japan.
Kohji OkamuraDepartment of Systems BioMedicine, National Research Institute for Child Health and Development, Setagaya-ku, Tokyo, Japan.
Akinori YaguchiDepartment of Pediatric Hematology and Oncology Research, National Research Institute for Child Health and Development, Setagaya-ku, Tokyo, Japan.
Kazuki TeradaDepartment of Pediatric Hematology and Oncology Research, National Research Institute for Child Health and Development, Setagaya-ku, Tokyo, Japan.
Yuya SaitoDepartment of Pediatric Hematology and Oncology Research, National Research Institute for Child Health and Development, Setagaya-ku, Tokyo, Japan.
Ai YoshimiDepartment of Pediatric Hematology and Oncology Research, National Research Institute for Child Health and Development, Setagaya-ku, Tokyo, Japan.
Hiroko Ogata-KawataDepartment of Maternal-Fetal Biology, National Research Institute for Child Health and Development, Setagaya-ku, Tokyo, Japan.
Hiromi SakamotoDivision of Genetics, National Cancer Center Research Institute, Chuo-ku, Tokyo, Japan.
Motohiro KatoDepartment of Pediatric Hematology and Oncology Research, National Research Institute for Child Health and Development, Setagaya-ku, Tokyo, Japan.
Junya FujimuraDepartment of Pediatrics and Adolescent Medicine, Juntendo University Graduate School of Medicine, Bunkyo-ku, Tokyo, Japan.
Moeko HinoDepartment of Pediatrics, Chiba University Graduate School of Medicine, Chiba-shi, Chiba, Japan.
Akitoshi KinoshitaDepartment of Pediatrics, St. Marianna University School of Medicine, Kawasaki-shi, Kanagawa, Japan.
Harumi KakudaDepartment of Haematology/Oncology, Chiba Children's Hospital, Chiba-shi, Chiba, Japan.
Hidemitsu KurosawaDepartment of Pediatrics, Dokkyo Medical University, Mibu, Tochigi, Japan.
Keisuke KatoDivision of Pediatric Hematology and Oncology, Ibaraki Children's Hospital, Mito-shi, Ibaraki, Japan.
Ryosuke KajiwaraDepartment of Pediatrics, Yokohama City University Hospital, Yokohama-shi, Kanagawa, Japan.
Koichi MoriwakiDepartment of Pediatrics, Saitama Medical Center, Saitama Medical University, Kawagoe-shi, Saitama, Japan.
Tsuyoshi MorimotoDepartment of Pediatrics, Tokai University School of Medicine, Isehara-shi, Kanagawa, Japan.
Kozue NakamuraDepartment of Pediatrics, Teikyo University School of Medicine, Itabashi-ku, Tokyo, Japan.
Yasushi NoguchiDepartment of Pediatrics, Japanese Red Cross Narita Hospital, Narita-shi, Chiba, Japan.
Tomoo OsumiDepartment of Pediatric Hematology and Oncology Research, National Research Institute for Child Health and Development, Setagaya-ku, Tokyo, Japan.
Kazuo SakashitaDepartment of Hematology/Oncology, Nagano Children's Hospital, Azumino-shi, Nagano, Japan.
Junko TakitaDepartment of Pediatrics, Graduate School of Medicine, University of Tokyo, Bunkyo-ku, Tokyo, Japan.
Yuki YuzaDepartment of Hematology/Oncology, Tokyo Metropolitan Children's Medical Center, Fuchu-shi, Tokyo, Japan.
Koich MatsudaLaboratory of Clinical Sequence, Department of Computational biology and medical Sciences, Graduate school of Frontier Sciences, The University of Tokyo, Minato-ku, Tokyo, Japan.
Teruhiko YoshidaDivision of Genetics, National Cancer Center Research Institute, Chuo-ku, Tokyo, Japan.
Kenji MatsumotoDepartment of Allergy and Clinical Immunology, National Research Institute for Child Health and Development, Setagaya-ku, Tokyo, Japan.
Kenichiro HataDepartment of Maternal-Fetal Biology, National Research Institute for Child Health and Development, Setagaya-ku, Tokyo, Japan.
Michiaki KuboLaboratory for Genotyping Development, Center for Integrative Medical Sciences (IMS), RIKEN, Yokohama-shi, Kanagawa, Japan.
Yoichi MatsubaraNational Research Institute for Child Health and Development, Setagaya-ku, Tokyo, Japan.
Takashi FukushimaDepartment of Child Health, Faculty of Medicine, University of Tsukuba, Tsukuba-shi, Ibaraki, Japan.
Katsuyoshi KohDepartment of Hematology/Oncology, Saitama Children's Medical Center, Saitama-shi, Saitama, Japan.
Atsushi ManabeDepartment of Pediatrics, St. Luke's International Hospital, Chuo-ku, Tokyo, Japan.
Akira OharaDepartment of Pediatrics, Toho University Omori Medical Center, Ohta-ku, Tokyo, Japan.
Nobutaka KiyokawaDepartment of Pediatric Hematology and Oncology Research, National Research Institute for Child Health and Development, Setagaya-ku, Tokyo, Japan kiyokawa-n@ncchd.go.jp oki-kn@ncchd.go.jp.
Tokyo Children’s Cancer Study Group (TCCSG)
National Center For Child Health and Development · JPIbaraki Children's Hospital · JPRIKEN Center for Integrative Medical Sciences · JPSt. Luke's International Hospital · JPThe University of Tokyo · JPTokyo Metropolitan Children's Medical Center · JPChiba Hospital · JPChiba University · JPDokkyo Medical University · JPJapanese Red Cross Narita Hospital · JPJuntendo University · JPNagano Children's Hospital · JPSaitama Children's Medical Center · JPSaitama Medical University · JPSt. Marianna University School of Medicine · JPTeikyo University · JPToho University · JPTokai University · JPUniversity of Tsukuba · JPYokohama City University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fusion genes involving ZNF384 have recently been identified in B-cell precursor acute lymphoblastic leukemia, and 7 fusion partners have been reported. We further characterized this type of fusion gene by whole transcriptome sequencing and/or polymerase chain reaction. In addition to previously reported genes, we identified BMP2K as a novel fusion partner for ZNF384 Including the EP300-ZNF384 that we reported recently, the total frequency of ZNF384-related fusion genes was 4.1% in 291 B-cell precursor acute lymphoblastic leukemia patients enrolled in a single clinical trial, and TCF3-ZNF384 was the most recurrent, with a frequency of 2.4%. The characteristic immunophenotype of weak CD10 and aberrant CD13 and/or CD33 expression was revealed to be a common feature of the leukemic cells harboring ZNF384-related fusion genes. The signature gene expression profile in TCF3-ZNF384-positive patients was enriched in hematopoietic stem cell features and related to that of EP300-ZNF384-positive patients, but was significantly distinct from that of TCF3-PBX1-positive and ZNF384-fusion-negative patients. However, clinical features of TCF3-ZNF384-positive patients are markedly different from those of EP300-ZNF384-positive patients, exhibiting higher cell counts and a younger age at presentation. TCF3-ZNF384-positive patients revealed a significantly poorer steroid response and a higher frequency of relapse, and the additional activating mutations in RAS signaling pathway genes were detected by whole exome analysis in some of the cases. Our observations indicate that ZNF384-related fusion genes consist of a distinct subgroup of B-cell precursor acute lymphoblastic leukemia with a characteristic immunophenotype, while the clinical features depend on the functional properties of individual fusion partners.

Indexed as

ImmunophenotypingAdolescentBiomarkers, TumorChildChild, PreschoolCluster AnalysisComputational BiologyFemaleGene Expression ProfilingGene FrequencyHigh-Throughput Nucleotide SequencingHumansInfantInfant, NewbornKaplan-Meier EstimateMaleBiomarkers, TumorOncogene Proteins, FusionTrans-ActivatorsZNF384 protein, human

Identifiers

PMID27634205
PMCPMC5210242
OpenAlexW2520574697

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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.