Evidence map›Paper›PMID 30635632›Full record

ArticleLeukemia2019

Genetic and transcriptional landscape of plasma cells in POEMS syndrome.

Yuhei Nagao, Naoya Mimura, June Takeda, Kenichi Yoshida, Yusuke Shiozawa, Motohiko Oshima, Kazumasa Aoyama, Atsunori Saraya, Shuhei Koide, Ola Rizq and 25 more

Abstract read
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In one paragraph

Article in Leukemia, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

15 citing papers in PubMed, 34 citations in OpenAlex.

  1. Review
  2. Review
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  4. Article
  5. Article
  6. Update on the POEMS syndrome.Blood research · 2022
    Review
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  8. Article
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  10. 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

35 authors at 6 institutions in 1 country.

Yuhei NagaoDepartment of Hematology, Chiba University Hospital, Chiba, Japan.
Naoya MimuraDepartment of Hematology, Chiba University Hospital, Chiba, Japan. naoyamimura@chiba-u.jp.
June TakedaDepartment of Pathology and Tumor Biology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Kenichi YoshidaDepartment of Pathology and Tumor Biology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Yusuke ShiozawaDepartment of Pediatrics, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Motohiko OshimaDepartment of Cellular and Molecular Medicine, Chiba University Graduate School of Medicine, Chiba, Japan.
Kazumasa AoyamaDepartment of Cellular and Molecular Medicine, Chiba University Graduate School of Medicine, Chiba, Japan.
Atsunori SarayaDepartment of Cellular and Molecular Medicine, Chiba University Graduate School of Medicine, Chiba, Japan.
Shuhei KoideDepartment of Cellular and Molecular Medicine, Chiba University Graduate School of Medicine, Chiba, Japan.
Ola RizqDepartment of Cellular and Molecular Medicine, Chiba University Graduate School of Medicine, Chiba, Japan.
Yoshinori HasegawaDepartment of Research and Development, Kazusa DNA Research Institute, Kisarazu, Japan.
Yuichi ShiraishiHuman Genome Center, Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
Kenichi ChibaHuman Genome Center, Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
Hiroko TanakaHuman Genome Center, Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
Dai NishijimaHuman Genome Center, Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
Yusuke IsshikiDepartment of Hematology, Chiba University Hospital, Chiba, Japan.
Kensuke KayamoriDepartment of Hematology, Chiba University Hospital, Chiba, Japan.
Chika Kawajiri-ManakoDepartment of Hematology, Chiba University Hospital, Chiba, Japan.
Nagisa Oshima-HasegawaDepartment of Hematology, Chiba University Hospital, Chiba, Japan.
Shokichi TsukamotoDepartment of Hematology, Chiba University Hospital, Chiba, Japan.
Shio MitsukawaDepartment of Hematology, Chiba University Hospital, Chiba, Japan.
Yusuke TakedaDepartment of Hematology, Chiba University Hospital, Chiba, Japan.
Chikako OhwadaDepartment of Hematology, Chiba University Hospital, Chiba, Japan.
Masahiro TakeuchiDepartment of Hematology, Chiba University Hospital, Chiba, Japan.
Tohru IsekiDepartment of Hematology, Chiba University Hospital, Chiba, Japan.
Sonoko MisawaDepartment of Neurology, Chiba University Graduate School of Medicine, Chiba, Japan.
Satoru MiyanoHuman Genome Center, Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
Osamu OharaDepartment of Technology Development, Kazusa DNA Research Institute, Kisarazu, Japan.ORCID http://orcid.org/0000-0002-3328-9571
Koutaro YokoteDepartment of Clinical Cell Biology and Medicine, Chiba University Graduate School of Medicine, Chiba, Japan.
Emiko SakaidaDepartment of Hematology, Chiba University Hospital, Chiba, Japan.
Satoshi KuwabaraDepartment of Neurology, Chiba University Graduate School of Medicine, Chiba, Japan.
Masashi SanadaDepartment of Advanced Diagnosis, Clinical Research Center, National Hospital Organization Nagoya Medical Center, Nagoya, Japan.
Atsushi IwamaDepartment of Cellular and Molecular Medicine, Chiba University Graduate School of Medicine, Chiba, Japan.
Seishi OgawaDepartment of Pathology and Tumor Biology, Graduate School of Medicine, Kyoto University, Kyoto, Japan. sogawa-tky@umin.ac.jp.
Chiaki NakasekoDepartment of Hematology, Chiba University Hospital, Chiba, Japan. chiaki-nakaseko@faculty.chiba-u.jp.ORCID http://orcid.org/0000-0003-1175-226X
Chiba University · JPChiba University Hospital · JPThe University of Tokyo · JPKyoto University · JPKazusa DNA Research Institute · JPNational Hospital Organization · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

POEMS syndrome is a rare paraneoplastic disease associated with monoclonal plasma cells; however, the pathogenic importance of plasma cells remains unclear. We performed comprehensive genetic analyses of plasma cells in 20 patients with POEMS syndrome. Whole exome sequencing was performed in 11 cases and found a total of 308 somatic mutations in 285 genes. Targeted sequencing was performed in all 20 cases and identified 20 mutations in 7 recurrently mutated genes, namely KLHL6, LTB, EHD1, EML4, HEPHL1, HIPK1, and PCDH10. None of the driver gene mutations frequently found in multiple myeloma (MM) such as NRAS, KRAS, BRAF, and TP53 was detected. Copy number analysis showed chromosomal abnormalities shared with monoclonal gammopathy of undetermined significance (MGUS), suggesting a partial overlap in the early development of MGUS and POEMS syndrome. RNA sequencing revealed a transcription profile specific to POEMS syndrome when compared with normal plasma cells, MGUS and MM. Unexpectedly, disease-specific VEGFA expression was not increased in POEMS syndrome. Our study illustrates that the genetic and transcriptional profiles of plasma cells in POEMS syndrome are distinct from MM and MGUS, indicating unique function of clonal plasma cells in its pathogenesis.

Indexed as

Gene Expression ProfilingMutationAdolescentAdultAgedAntineoplastic Combined Chemotherapy ProtocolsBiomarkers, TumorExome SequencingFemaleHigh-Throughput Nucleotide SequencingHumansMaleMiddle AgedMonoclonal Gammopathy of Undetermined SignificanceMultiple MyelomaNeoplasm Recurrence, LocalBiomarkers, Tumor

Identifiers

PMID30635632
OpenAlexW2910178265

What OpenQuestion holds

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Registered trials

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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.