Evidence map›Paper›PMID 11891187›Full record

ArticleThe American journal of pathology2002

In situ analysis of the variable heavy chain gene of an IgM/IgG-expressing follicular lymphoma: evidence for interfollicular trafficking of tumor cells.

Wilhelmina M Aarts, Richard J Bende, Jan-Willem Vaandrager, Philip M Kluin, Anton W Langerak, Steven T Pals, Carel J M van Noesel

Abstract readCase Reports
In one paragraph

Article in The American journal of pathology, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Article
  2. Pathogenesis of follicular lymphoma.The Journal of clinical investigation · 2012
    Review
  3. Review
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.

Wilhelmina M AartsDepartment of Pathology, Academic MedicalCenter, Amsterdam, the Netherlands.
Richard J Bende
Jan-Willem Vaandrager
Philip M Kluin
Anton W Langerak
Steven T Pals
Carel J M van Noesel

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It is generally assumed that follicular lymphomas (FL) not only morphologically resemble normal germinal centers but have retained some functional characteristics of their non-neoplastic counterparts as well. Recent IgV gene analyses on a panel of FLs however, strongly suggested that FLs do not retain the capacity of somatic hypermutation and are not being selected on basis of the quality of their mIgV regions. To extend these findings, we investigated the follicular organization and class switching in a FL that consisted of both IgM- and IgG-expressing tumor cells with a high somatic mutation load and significant intraclonal V(H) gene diversity. V(H)-C(mu) and V(H)-Cgamma gene transcripts were amplified and sequenced from samples of approximately 50 tumor cells, isolated from frozen tissue sections by laser microdissection. We identified many different subclones and obtained limited evidence of subclone dominance in individual follicles. Remarkably, several subclones were found scattered over different follicles. All samples contained IgM- and IgG-expressing tumor cells with, in general, non-identical mutation patterns, which is not in support of ongoing class switching. Accordingly, no switch circle recombination products were found. The findings indicate that the neoplastic follicles lack the organization and functions typical of reactive germinal centers.

Indexed as

Genes, ImmunoglobulinCell MovementFemaleHumansImmunoglobulin Class SwitchingImmunoglobulin GImmunoglobulin Heavy ChainsImmunoglobulin MImmunoglobulin Variable RegionLasersLymph NodesLymphoma, FollicularMicromanipulationMiddle AgedImmunoglobulin GImmunoglobulin Heavy ChainsImmunoglobulin MImmunoglobulin Variable Region

Identifiers

PMID11891187
PMCPMC1867185

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.