Evidence map›Paper›PMID 27416831›Full record

ArticleCancer immunology, immunotherapy : CII2016

DNA methyltransferase inhibition increases efficacy of adoptive cellular immunotherapy of murine breast cancer.

Krista P Terracina, Laura J Graham, Kyle K Payne, Masoud H Manjili, Annabel Baek, Sheela R Damle, Harry D Bear

Abstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.0field-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

31 citing papers in PubMed, 55 citations in OpenAlex.

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  14. Genetically Modified Cellular Therapies for Malignant Gliomas.International journal of molecular sciences · 2021
    Review
  15. Article
  16. Epigenetic strategies to boost CAR T cell therapy.Molecular therapy : the journal of the American Society of Gene Therapy · 2021
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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

7 authors at 2 institutions in 1 country.

Krista P TerracinaDepartment of Surgery, Virginia Commonwealth University, Richmond, VA, USA.
Laura J GrahamDepartment of Surgery, Virginia Commonwealth University, Richmond, VA, USA.
Kyle K PayneTumor Microenvironment and Metastasis Program, The Wistar Institute, Philadelphia, PA, USA.
Masoud H ManjiliDepartment of Microbiology and Immunology, Virginia Commonwealth University, Richmond, VA, USA.
Annabel BaekMassey Cancer Center, School of Medicine, Virginia Commonwealth University, West Hospital 7-402, 1200 East Broad Street, PO Box 980011, Richmond, VA, 23298-0011, USA.
Sheela R DamleDepartment of Microbiology and Immunology, Virginia Commonwealth University, Richmond, VA, USA.
Harry D BearDepartment of Surgery, Virginia Commonwealth University, Richmond, VA, USA. hdbear@vcu.edu.
Virginia Commonwealth University · USThe Wistar Institute · US

Funding

Virus Vector Shared ResourceP30CA016059 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI Kim Felder Rhoads · 1985 to 2026
$51.0M
POSTDOCTORAL TRAINING PROGRAM IN CANCER BIOLOGYT32CA085159 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI GINDER, GORDON D · 2000 to 2011
$2.0M
Mast cell mediators augment the immunoregulatory function of MDSCs.F30CA192836 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI DAMLE, SHEELA RUBY · 2015 to 2018
$169k
NCI NIH HHS F30 CA192836NCI NIH HHS P30 CA016059NCI NIH HHS T32 CA085159
6 · The paper itself

Abstract

Adoptive T cell immunotherapy is a promising approach to cancer treatment that currently has limited clinical applications. DNA methyltransferase inhibitors (DNAMTi) have known potential to affect the immune system through multiple mechanisms that could enhance the cytotoxic T cell responses, including: upregulation of tumor antigen expression, increased MHC class I expression, and blunting of myeloid derived suppressor cells (MDSCs) expansion. In this study, we have investigated the effect of combining the DNAMTi, decitabine, with adoptive T cell immunotherapy in the murine 4T1 mammary carcinoma model. We found that expression of neu, MHC class I molecules, and several murine cancer testis antigens (CTA) was increased by decitabine treatment of 4T1 cells in vitro. Decitabine also increased expression of multiple CTA in two human breast cancer cell lines. Decitabine-treated 4T1 cells stimulated greater IFN-gamma release from tumor-sensitized lymphocytes, implying increased immunogenicity. Expansion of CD11b + Gr1 + MDSC in 4T1 tumor-bearing mice was significantly diminished by decitabine treatment. Decitabine treatment improved the efficacy of adoptive T cell immunotherapy in mice with established 4T1 tumors, with greater inhibition of tumor growth and an increased cure rate. Decitabine may have a role in combination with existing and emerging immunotherapies for breast cancer.

Indexed as

AnimalsAntimetabolites, AntineoplasticAzacitidineBreast NeoplasmsCell Line, TumorDecitabineDNA Modification MethylasesEnzyme InhibitorsFemaleHumansImmunotherapy, AdoptiveMammary Neoplasms, ExperimentalMCF-7 CellsMiceMice, Inbred BALB CT-LymphocytesAntimetabolites, AntineoplasticAzacitidineDecitabineDNA Modification MethylasesEnzyme InhibitorsDecitabineEpigeneticImmunotherapyMyeloid derived suppressor cellsT lymphocytes

Identifiers

PMID27416831
PMCPMC4996686
OpenAlexW2461195258

What OpenQuestion holds

Textmetadata
LicenceTDM
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.