Evidence map›Paper›PMID 19347041›Full record

ArticlePloS one2009

RNAi-mediated c-Rel silencing leads to apoptosis of B cell tumor cells and suppresses antigenic immune response in vivo.

Wenzhi Tian, Hsiou-Chi Liou

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.6field-weighted citation impact, top 15% 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

15 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Article
  3. Regulation of B-cell function by NF-kappaB c-Rel in health and disease.Cellular and molecular life sciences : CMLS · 2020
    Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. 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

2 authors at 1 institution in 1 country.

Wenzhi TianDivision of Immunology, Department of Medicine, Weill Medical College of Cornell University, New York, New York, USA.
Hsiou-Chi Liou
Cornell University · US

Funding

Mechanism of cell cycle and oncogenesis by c RelR01CA090405 · NCI · WEILL MEDICAL COLLEGE OF CORNELL UNIV · PI LIOU, HSIOU-CHI · 2001 to 2005
$1.4M
C-REL GENE AND IMMUNE REGULATIONR01CA068155 · NCI · WEILL MEDICAL COLLEGE OF CORNELL UNIV · PI LIOU, HSIOU-CHI · 1997 to 2001
$537k
C-REL GENE AND IMMUNE REGULATIONR55CA068155 · NCI · WEILL MEDICAL COLLEGE OF CORNELL UNIV · PI LIOU, HSIOU-CHI · 1995 to 1995
–
NCI NIH HHS CA68155NCI NIH HHS CA90405NCI NIH HHS R01 CA090405
6 · The paper itself

Abstract

c-Rel is a member of the Rel/NF-kappaB transcription factor family and is predominantly expressed in lymphoid and myeloid cells, playing a critical role in lymphocyte proliferation and survival. Persistent activation of the c-Rel signal transduction pathway is associated with allergies, inflammation, autoimmune diseases, and a variety of human malignancies. To explore the potential of targeting c-Rel as a therapeutic agent for these disorders, we designed a small interfering RNA (siRNA) to silence c-Rel expression in vitro and in vivo. C-Rel-siRNA expression via a retroviral vector in a B cell tumor cell line leads to growth arrest and apoptosis of the tumor cells. Silencing c-Rel in primary B cells in vitro compromises their proliferative and survival response to CD40 activation signals, similar to the impaired response of c-Rel knockout B cells. Most important, in vivo silencing of c-Rel results in significant impairment in T cell-mediated immune responses to antigenic stimulation. Our study thus validates the efficacy of c-Rel-siRNA, and suggests the development of siRNA-based therapy, as well as small molecular inhibitors for the treatment of B cell tumors as well as autoimmune diseases.

Indexed as

Gene SilencingRNA InterferenceAnimalsAntigens, NeoplasmApoptosisBase SequenceB-LymphocytesCell LineMiceNeoplasms, ExperimentalNIH 3T3 CellsProto-Oncogene Proteins c-relRNA, Small InterferingAntigens, NeoplasmProto-Oncogene Proteins c-relRNA, Small Interfering

Identifiers

PMID19347041
PMCPMC2661141
OpenAlexW2025886777

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.