Evidence map›Paper›PMID 37586844›Full record

ArticleMolecular cancer therapeutics2023

Radiotherapy-induced Immune Response Enhanced by Selective HDAC6 Inhibition.

Satish Kumar R Noonepalle, Scott Grindrod, Nima Aghdam, Xintang Li, Maria Gracia-Hernandez, Christian Zevallos-Delgado, Mira Jung, Alejandro Villagra, Anatoly Dritschilo

Open access · greenAbstract read
In one paragraph

Article in Molecular cancer therapeutics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

11 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
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  4. Epigenetic programming of macrophages across inflammatory and malignant diseases.Naunyn-Schmiedeberg's archives of pharmacology · 2026
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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

9 authors at 2 institutions in 1 country.

Satish Kumar R Noonepalle *Department of Oncology, Georgetown University Lombardi Comprehensive Cancer Center, Washington, District of Columbia.ORCID 0000-0002-0346-3882
Scott Grindrod *Shuttle Pharmaceuticals, Inc., Rockville, Maryland.ORCID 0000-0002-6999-9604
Nima AghdamDepartment of Radiation Medicine, Georgetown University Medical Center, Washington, District of Columbia.ORCID 0000-0001-8078-0438
Xintang LiDepartment of Oncology, Georgetown University Lombardi Comprehensive Cancer Center, Washington, District of Columbia.ORCID 0009-0002-4974-4732
Maria Gracia-HernandezDepartment of Oncology, Georgetown University Lombardi Comprehensive Cancer Center, Washington, District of Columbia.ORCID 0000-0001-9334-8177
Christian Zevallos-DelgadoDepartment of Oncology, Georgetown University Lombardi Comprehensive Cancer Center, Washington, District of Columbia.ORCID 0000-0001-7078-3782
Mira JungDepartment of Radiation Medicine, Georgetown University Medical Center, Washington, District of Columbia.ORCID 0000-0001-7146-5217
Alejandro VillagraDepartment of Oncology, Georgetown University Lombardi Comprehensive Cancer Center, Washington, District of Columbia.ORCID 0000-0001-9346-8355
Anatoly DritschiloShuttle Pharmaceuticals, Inc., Rockville, Maryland.ORCID 0000-0002-7120-097X
Georgetown University · USShuttle Pharmaceuticals (United States) · US

Funding

Development of selective HDAC6 inhibitors to improve cancer immunotherapyR01CA249248 · NCI · GEORGE WASHINGTON UNIVERSITY · PI VILLAGRA, ALEJANDRO V, WARDROP, DUNCAN JOHN · 2021 to 2025
$3.0M
NCI NIH HHS R01 CA249248
6 · The paper itself

Abstract

Radiotherapy is a curative cancer treatment modality that imparts damage to cellular DNA, induces immunogenic cell death, and activates antitumor immunity. Despite the radiotherapy-induced direct antitumor effect seen within the treated volume, accumulating evidence indicates activation of innate antitumor immunity. Acute proinflammatory responses mediated by anticancer M1 macrophages are observed in the immediate aftermath following radiotherapy. However, after a few days, these M1 macrophages are converted to anti-inflammatory and pro-cancer M2 phenotype, leading to cancer resistance and underlying potential tumor relapse. Histone deacetylase 6 (HDAC6) plays a crucial role in regulating macrophage polarization and innate immune responses. Here, we report targeting HDAC6 function with a novel selective inhibitor (SP-2-225) as a potential therapeutic candidate for combination therapy with radiotherapy. This resulted in decreased tumor growth and enhanced M1/M2 ratio of infiltrating macrophages within tumors. These observations support the use of selective HDAC6 inhibitors to improve antitumor immune responses and prevent tumor relapse after radiotherapy.

Indexed as

NeoplasmsHistone Deacetylase 6HumansImmunity, InnateMacrophagesRecurrenceHDAC6 protein, humanHistone Deacetylase 6

Identifiers

PMID37586844
PMCPMC10878032
OpenAlexW4385852841

What OpenQuestion holds

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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.