Evidence map›Paper›PMID 38538317›Full record

ArticleJournal of clinical and experimental hematopathology : JCEH2024

Diverse B-cell tumors associated with t(14;19)(q32;q13)/IGH::BCL3 identified by G-banding and fluorescence in situ hybridization.

Hitoshi Ohno, Fumiyo Maekawa, Masahiko Hayashida, Miho Nakagawa, Katsuhiro Fukutsuka, Mitsuko Matsumura, Kayo Takeoka, Wataru Maruyama, Naoya Ukyo, Shinji Sumiyoshi and 2 more

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical and experimental hematopathology : JCEH, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. 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

12 authors at 3 institutions in 1 country.

Hitoshi OhnoTenri Institute of Medical Research, Tenri Hospital, Tenri, Japan.
Fumiyo MaekawaTenri Institute of Medical Research, Tenri Hospital, Tenri, Japan.
Masahiko HayashidaTenri Institute of Medical Research, Tenri Hospital, Tenri, Japan.
Miho NakagawaTenri Institute of Medical Research, Tenri Hospital, Tenri, Japan.
Katsuhiro FukutsukaTenri Institute of Medical Research, Tenri Hospital, Tenri, Japan.
Mitsuko MatsumuraTenri Institute of Medical Research, Tenri Hospital, Tenri, Japan.
Kayo TakeokaTenri Institute of Medical Research, Tenri Hospital, Tenri, Japan.
Wataru MaruyamaDepartment of Hematology, Tenri Hospital, Tenri, Japan.
Naoya UkyoDepartment of Hematology, Tenri Hospital, Tenri, Japan.
Shinji SumiyoshiDepartment of Diagnostic Pathology, Tenri Hospital, Tenri, Japan.
Yasuhiro TanakaDepartment of Hematology, Shinko Hospital, Tenri, Japan.
Hironori HagaDepartment of Diagnostic Pathology, Graduate School of Medicine, Kyoto University, Tenri, Japan.
Tenri Hospital · JPKyoto University · JPShinko Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We characterized 5 B-cell tumors carrying t(14;19)(q32;q13) that creates the IGH::BCL3 fusion gene. The patients' ages ranged between 55 and 88 years. Two patients presented with progression or recurrence of B-cell chronic lymphocytic leukemia (B-CLL)/small lymphocytic lymphoma (SLL), two with diffuse large B-cell lymphoma (DLBCL) of non-germinal center B-like phenotype, and the remaining one with composite angioimmunoblastic T-cell lymphoma and Epstein-Barr virus-positive DLBCL. The presence of t(14;19)(q32;q13) was confirmed by fluorescence in situ hybridization (FISH), showing colocalization of 3' IGH and 3' BCL3 probes on der(14)t(14;19) and 5' BCL3 and 5' IGH probes on der(19)t(14;19). One B-CLL case had t(2;14)(p13;q32)/IGH::BCL11A, and 2 DLBCL cases had t(8;14)(q24;q32) or t(8;11;14)(q24;q11;q32), both of which generated IGH::MYC by FISH, and showed nuclear expression of MYC and BCL3 by immunohistochemistry. The IGH::BCL3 fusion gene was amplified by long-distance polymerase chain reaction in 2 B-CLL/SLL cases and the breakpoints occurred immediately 5' of BCL3 exon 1 and within the switch region associated with IGHA1. The 5 cases shared IGHV preferentially used in B-CLL cells, but the genes were unmutated in 2 B-CLL/SLL cases and significantly mutated in the remaining 3. B-cell tumors with t(14;19)(q32;q13) can be divided into B-CLL/SLL and DLBCL groups, and the anatomy of IGH::BCL3 in the latter may be different from that of the former.

Indexed as

Epstein-Barr Virus InfectionsLeukemia, Lymphocytic, Chronic, B-CellLymphoma, Large B-Cell, DiffuseAgedAged, 80 and overChromosomes, Human, Pair 14Herpesvirus 4, HumanHumansIn Situ Hybridization, FluorescenceMiddle AgedTranslocation, Genetic19)(q32q13)/IGH::BCL3, B-cell chronic lymphocytic leukemia/small lymphocytic lymphoma, diffuse large B-cell lymphoma, fluorescence in situ hybridization, immunohistochemistryt(14

Identifiers

PMID38538317
PMCPMC11079985
OpenAlexW4393216157

What Socratic holds

Textmetadata
LicenceCC BY-NC-SA
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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 Socratic graph.