Evidence map›Paper›PMID 12495470›Full record

ArticleJapanese journal of cancer research : Gann2002

Primary malignant lymphoma of the brain: mutation pattern of rearranged immunoglobulin heavy chain gene.

Sumio Endo, Shu-Jing Zhang, Takafumi Saito, Mitsuo Kouno, Toshihiko Kuroiwa, Kazuo Washiyama, Toshiro Kumanishi

Abstract read
In one paragraph

Article in Japanese journal of cancer research : Gann, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

2 citing papers in PubMed.

  1. Article
  2. 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

7 authors.

Sumio EndoMolecular Neuropathology, Brain Research Institute, Niigata University, Niigata 951-8585, Japan.
Shu-Jing Zhang
Takafumi Saito
Mitsuo Kouno
Toshihiko Kuroiwa
Kazuo Washiyama
Toshiro Kumanishi

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Using reverse transcription-polymerase chain reaction (RT-PCR), six primary brain lymphomas, pathologically diagnosed as diffuse large B-cell lymphoma, were examined for rearranged VH-D-JH sequences of the immunoglobulin heavy chain gene, focusing on somatic mutations and intraclonal heterogeneity. The reliability of the isolated PCR clones was confirmed by in situ hybridization (ISH) with complementarity-determining region (CDR) 3 oligonucleotide probes. Sequence analysis of the PCR clones revealed a high frequency of somatic mutation, ranging from 8.8 to 27.3% (mean 18.2%) in the VH gene segments in all the lymphomas. A significantly lower frequency of replacement (R) mutations than expected was also seen in their frameworks (FRs) in all cases. These findings suggested that the precursor cells were germinal center (GC)-related cells in these lymphomas. However, despite extensive cloning experiments, intraclonal heterogeneity was not detected in any case except for one in which it could not be ruled out. Thus, it seemed likely that all of our brain lymphomas were derived from GC-related cells and that at least most of them were from post-GC cells.

Indexed as

Gene RearrangementGenes, ImmunoglobulinMutationAgedBase SequenceBrain NeoplasmsFemaleHumansImmunoglobulin Heavy ChainsImmunoglobulin Variable RegionIn Situ HybridizationLymphoma, B-CellMaleMiddle AgedMolecular Sequence DataPolymerase Chain ReactionImmunoglobulin Heavy ChainsImmunoglobulin Variable Region

Identifiers

PMID12495470
PMCPMC5926927

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.