Evidence map›Paper›PMID 36882509›Full record

ArticleJournal of human genetics2023

Imaging flow cytometry-based multiplex FISH for three IGH translocations in multiple myeloma.

Taku Tsukamoto, Masaki Kinoshita, Kazuhiro Yamada, Hodaka Ito, Toshikazu Yamaguchi, Yoshiaki Chinen, Shinsuke Mizutani, Takahiro Fujino, Tsutomu Kobayashi, Yuji Shimura and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of human genetics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
3.5field-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

5 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 4 institutions in 1 country.

Taku TsukamotoDivision of Hematology & Oncology, Department of Medicine, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Masaki KinoshitaSysmex Corporation, Hyogo, Japan.
Kazuhiro YamadaSysmex Corporation, Hyogo, Japan.
Hodaka ItoGeneral Laboratory, Bio Medical Laboratories, Inc., Tokyo, Japan.
Toshikazu YamaguchiGeneral Laboratory, Bio Medical Laboratories, Inc., Tokyo, Japan.
Yoshiaki ChinenDivision of Hematology & Oncology, Department of Medicine, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Shinsuke MizutaniDivision of Hematology & Oncology, Department of Medicine, Kyoto Prefectural University of Medicine, Kyoto, Japan.ORCID http://orcid.org/0000-0002-6498-1755
Takahiro FujinoDivision of Hematology & Oncology, Department of Medicine, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Tsutomu KobayashiDivision of Hematology & Oncology, Department of Medicine, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Yuji ShimuraDivision of Hematology & Oncology, Department of Medicine, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Johji InazawaDepartment of Molecular Cytogenetics, Medical Research Institute, Tokyo Medical and Dental University, Tokyo, Japan. johinaz.cgen@mri.tmd.ac.jp.
Junya KurodaDivision of Hematology & Oncology, Department of Medicine, Kyoto Prefectural University of Medicine, Kyoto, Japan. junkuro@koto.kpu-m.ac.jp.ORCID http://orcid.org/0000-0001-6130-1550
Kyoto Prefectural University of Medicine · JPMedical & Biological Laboratories (Japan) · JPSysmex (Japan) · JPTokyo Medical and Dental University · JP

Funding

Japan Agency for Medical Research and Development (AMED) JP19ck0106516h0001
6 · The paper itself

Abstract

Three types of chromosomal translocations, t(4;14)(p16;q32), t(14;16)(q32;q23), and t(11;14)(q13;q32), are associated with prognosis and the decision making of therapeutic strategy for multiple myeloma (MM). In this study, we developed a new diagnostic modality of the multiplex FISH in immunophenotyped cells in suspension (Immunophenotyped-Suspension-Multiplex (ISM)-FISH). For the ISM-FISH, we first subject cells in suspension to the immunostaining by anti-CD138 antibody and, then, to the hybridization with four different FISH probes for genes of IGH, FGFR3, MAF, and CCND1 tagged by different fluorescence in suspension. Then, cells are analyzed by the imaging flow cytometry MI-1000 combined with the FISH spot counting tool. By this system of the ISM-FISH, we can simultaneously examine the three chromosomal translocations, i.e, t(4;14), t(14;16), and t(11;14), in CD138-positive tumor cells in more than 2.5 × 10

Indexed as

Multiple MyelomaChromosomes, Human, Pair 14Flow CytometryGene RearrangementHumansIn Situ Hybridization, FluorescenceTranslocation, Genetic

Identifiers

PMID36882509
PMCPMC10290952
OpenAlexW4323530959

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.