Evidence map›Paper›PMID 10229093›Full record

ArticleEuropean journal of immunology1999

Clonal evolution of B cells in transformation from low- to high-grade lymphoma.

A Matolcsy, E J Schattner, D M Knowles, P Casali

Open access · bronzeAbstract read
In one paragraph

Article in European journal of immunology, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
4.6field-weighted citation impact, top 5% 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

22 citing papers in PubMed, 90 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Richter's transformation in chronic lymphocytic leukemia.Current hematologic malignancy reports · 2007
    Review
  8. Article
  9. Recent advances in the diagnosis and therapy of Richter's syndrome.Medical oncology (Northwood, London, England) · 2007
    Review
  10. Article
  11. Review
  12. Review
  13. Immunohistochemistry in bone marrow pathology: a useful adjunct for morphologic diagnosis.Virchows Archiv : an international journal of pathology · 2005
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Molecular pathology of primary intraocular lymphoma.Transactions of the American Ophthalmological Society · 2003
    Article
  19. Article
  20. 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

4 authors at 1 institution in 2 countries.

A MatolcsyDepartment of Pathology, Weill Medical College of Cornell University New York, New York 10021, USA.
E J Schattner
D M Knowles
P Casali
Cornell University · US

Funding

SOMATIC HYPERMUTATION IN HUMAN B CELLSR01AR040908 · NIAMS · WEILL MEDICAL COLLEGE OF CORNELL UNIV · PI CASALI, PAOLO · 1992 to 2005
$1.8M
MOLECULAR IMMUNOBIOLOGY OF AIDS-LYMPHOMAR01CA068541 · NCI · WEILL MEDICAL COLLEGE OF CORNELL UNIV · PI CASALI, PAOLO · 1995 to 1998
–
NCI NIH HHS CA 68541NIAMS NIH HHS AR 40908NIAMS NIH HHS R01 AR040908
6 · The paper itself

Abstract

An outcome of low-grade B cell non-Hodgkins's lymphomas is the transformation to high-grade diffuse large B cell lymphomas (DLBL). To investigate the mechanisms of clonal evolution in the transformation to DLBL, we performed longitudinal molecular analyses of immunoglobulin (Ig), V(H)DJ(H) gene sequences expressed in cases of chronic lymphocytic leukemia (CLL), small lymphocytic lymphoma (SLL), and follicular lymphoma (FL) that transformed to DLBL. Among the neoplastic CLL and SLL cells and their respective high-grade transformants, there was no evidence for a clonotypic shift or acquired mutations in the expressed Ig V(H)DJ(H) gene segments, as further confirmed by a specific and sensitive PCR-single strand polymorphism analysis. In contrast, among the FL cells there was a high degree of intraclonal diversification with highly divergent V(H)DJ(H) gene sequences. Despite this intraclonal heterogeneity, the related DLBL expressed a collinear but unique V(H)DJ(H) gene sequence. The intraclonal genealogical tree for the FL case demonstrated that the DLBL emerged in association with unique V(H)DJ(H) gene mutational events. Among the intraclonal FL and related DLBL transformants, the nature and distribution of the Ig V(H)DJ(H) gene mutations were consistent with antigenic selection. Thus, clonal evolution in the transformation from low- to high-grade B cell lymphoma may involve distinct pathways which vary according to the cellular origin and the type of the progenitor B cell tumor.

Indexed as

Amino Acid SequenceBase SequenceB-LymphocytesGene RearrangementGenes, ImmunoglobulinHumansImmunoglobulin Heavy ChainsImmunoglobulin Joining RegionImmunoglobulin Variable RegionLymphoma, B-CellLymphoma, Non-HodgkinMolecular Sequence DataMutationImmunoglobulin Heavy ChainsImmunoglobulin Joining RegionImmunoglobulin Variable Region

Identifiers

PMID10229093
PMCPMC4625534
OpenAlexW2079162000

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.