Evidence map›Paper›PMID 12860928›Full record

ArticleThe Journal of experimental medicine2003

BCL6 controls the expression of the B7-1/CD80 costimulatory receptor in germinal center B cells.

Huifeng Niu, Giorgio Cattoretti, Riccardo Dalla-Favera

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

51 citing papers in PubMed, 98 citations in OpenAlex.

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  10. The PI3K pathway impacts stem gene expression in a set of glioblastoma cell lines.Journal of cancer research and clinical oncology · 2020
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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

3 authors at 1 institution in 1 country.

Huifeng NiuInstitute for Cancer Genetics, Columbia University, 1150 St. Nicholas Ave., New York, NY 10032, USA.
Giorgio Cattoretti
Riccardo Dalla-Favera
Cancer Genetics (United States) · US

Funding

The Role of BCL-6 in Berminal Center FormationP01CA092625 · NCI · DANA-FARBER CANCER INSTITUTE · PI SHIPP, MARGARET A · 2001 to 2011
$32.9M
AIDS-ASSOCIATED LYMPHOPROLIFERATIVE DISORDERS/MOLEC BIOR37CA037295 · NCI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI DALLA-FAVERA, RICCARDO · 1989 to 2011
$4.1M
AIDS ASSOCIATED LYMPHOPROLIFERATIVE DISORDERSR01CA037295 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI DALLA-FAVERA, RICCARDO · 1997 to 2001
$705k
MOLECULAR BIOLOGY OF AIDS-RELATED TUMORSU01CA037295 · NCI · NEW YORK UNIVERSITY · PI DALLA-FAVERA, RICCARDO · 1985 to 1988
–
NCI NIH HHS CA-37295NCI NIH HHS CA-92625NCI NIH HHS P01 CA092625NCI NIH HHS R01 CA037295NCI NIH HHS R37 CA037295
6 · The paper itself

Abstract

The BCL6 proto-oncogene encodes a transcriptional repressor required for the development of germinal centers (GCs) and implicated in the pathogenesis of GC-derived B cell lymphoma. Understanding the precise role of BCL6 in normal GC formation and in lymphomagenesis depends on the identification of genes that are direct targets of its transcriptional repression. Here we report that BCL6 directly controls the expression of B7-1/CD80, a costimulatory receptor involved in B-T cell interactions critical for the development of T cell-mediated antibody responses. Upon CD40 signaling, transcription of the CD80 gene is induced by the nuclear factor (NF)-kappaB transcription factor. Our results show that BCL6 prevents CD40-induced expression of CD80 by binding its promoter region in vivo and suppressing its transcriptional activation by NF-kappaB. Consistent with a physiologic role for BCL6 in suppressing CD80, the expression of these two genes is mutually exclusive in B cells, and BCL6-defective mice show increased expression of CD80 in B cells. The results suggest that BCL6 may directly control the ability of B cell to interact with T cells during normal GC development. In addition, these findings imply that T-B cell interactions may be disrupted in B cell lymphoma expressing deregulated BCL6 genes.

Indexed as

Antigens, CDB7-1 AntigenBase SequenceB-LymphocytesBurkitt LymphomaCell LineDNA-Binding ProteinsFlow CytometryGene Expression RegulationGenetic VectorsGerm-Line MutationHumansMolecular Sequence DataProto-Oncogene MasProto-Oncogene ProteinsProto-Oncogene Proteins c-bcl-6Antigens, CDB7-1 AntigenDNA-Binding ProteinsMAS1 protein, humanProto-Oncogene MasProto-Oncogene ProteinsProto-Oncogene Proteins c-bcl-6Transcription Factors

Identifiers

PMID12860928
PMCPMC2194068
OpenAlexW2009859686

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.