Evidence map›Paper›PMID 21239696›Full record

ArticleBlood2011

HDAC11 plays an essential role in regulating OX40 ligand expression in Hodgkin lymphoma.

Daniela Buglio, Noor M Khaskhely, Kui Shin Voo, Hector Martinez-Valdez, Yong-Jun Liu, Anas Younes

RetractedErratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in Blood, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 68 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed, 1 pooled it
3.6field-weighted citation impact, top 6% 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

68 citing papers in PubMed, 1 synthesis or guideline pooled it, 117 citations in OpenAlex.

  1. Pooled it
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  5. Review
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  12. HDAC11 displays neuropathological alterations and offers as a novel drug target for Alzheimer's disease.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2025
    Article
  13. Article
  14. Review
  15. Article
  16. Emerging role of HDAC11 in skeletal muscle biology.Frontiers in cell and developmental biology · 2024
    Article
  17. Article
  18. Article
  19. Article
  20. Digital spatial profiling of CD4Virchows Archiv : an international journal of pathology · 2023
    Article

8 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Daniela BuglioDepartments of Lymphoma and Myeloma, The University of Texas M. D. Anderson Cancer Center, Houston, TX, USA.
Noor M Khaskhely
Kui Shin Voo
Hector Martinez-Valdez
Yong-Jun Liu
Anas Younes
The University of Texas MD Anderson Cancer Center · US

Funding

TSLP Signaling in Dendritic Cells - Aim 3U19AI071130 · NIAID · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI LIU, YONG-JUN · 2006 to 2010
$6.1M
TSLP and Allergic InflammationR01AI061645 · NIAID · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI LIU, YONG-JUN · 2004 to 2008
$1.8M
Studies of germinal center B cell survivalR01AI065796 · NIAID · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI MARTINEZ-VALDEZ, HECTOR · 2005 to 2009
$1.7M
UT M.D. Anderson Cancer Center Lymphoma SPOREP50CA136411 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI KWAK, LARRY W · 2009 to 2011
$1.5M
Clinical Activity of 17-AAG in LymphomaR21CA117070 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI YOUNES, ANAS · 2006 to 2007
$431k
NCI NIH HHS 1R21CA117070-01NCI NIH HHS P50 CA136411NCI NIH HHS P50CA136411-01A1NCI NIH HHS R21 CA117070NIAID NIH HHS R01 AI061645NIAID NIH HHS R01 AI061645-01NIAID NIH HHS R01 AI065796NIAID NIH HHS R01 AI065796-05NIAID NIH HHS U19 AI071130NIAID NIH HHS U19AI071130-01
6 · The paper itself

Abstract

In Hodgkin lymphoma (HL), the malignant cells are surrounded by a large number of reactive infiltrating inflammatory cells, including OX40-expressing T cells and interleukin 10 (IL-10)-producing regulatory T (T-reg) cells. These T-reg cells can suppress the immune response and thus contribute to the maintenance of immune tolerance and to insufficient antitumor response. The engagement of OX40L with the OX40 receptor is essential for the generation of antigen-specific memory T cells and for the induction of host antitumor immunity. In the present study, we investigated whether histone deacetylase inhibitors (HDACis) may induce a favorable antitumor immune response by regulating the expression of OX40L in HL. We found that HDACis up-regulated OX40L surface expression in HL cell lines in a dose-dependent manner. Small interfering RNAs (siRNAs) that selectively inhibited HDAC11 expression, significantly up-regulated OX40L and induced apoptosis in HL cell lines, and silencing HDAC11 transcripts increased the production of tumor necrosis-α (TNF-α) and IL-17 in the supernatants of HL cells. Furthermore, HDACI-induced OX40L inhibited the generation of IL-10-producing type 1 T-reg cells. These results demonstrate for the first time that HDAC11 plays an essential role in regulating OX40L expression. Pharmacologic inhibition of HDAC11 may produce a favorable antitumor immune response in patients with HL.

Indexed as

Blotting, WesternCell Line, TumorCell SeparationEnzyme-Linked Immunosorbent AssayFlow CytometryGene ExpressionGene Expression Regulation, NeoplasticHistone Deacetylase InhibitorsHistone DeacetylasesHodgkin DiseaseHumansOX40 LigandReverse Transcriptase Polymerase Chain ReactionRNA, Small InterferingTransfectionHDAC11 protein, humanHistone Deacetylase InhibitorsHistone DeacetylasesOX40 LigandRNA, Small Interfering

Identifiers

PMID21239696
PMCPMC3062301
OpenAlexW1981869629

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.