Evidence map›Paper›PMID 23671644›Full record

ArticlePloS one2013

Low dose decitabine treatment induces CD80 expression in cancer cells and stimulates tumor specific cytotoxic T lymphocyte responses.

Li-Xin Wang, Zhen-Yang Mei, Ji-Hao Zhou, Yu-Shi Yao, Yong-Hui Li, Yi-Han Xu, Jing-Xin Li, Xiao-Ning Gao, Min-Hang Zhou, Meng-Meng Jiang and 10 more

3 registry-linked trialsOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this map. Cited by 74 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
74citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 8% 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.

NCT02662647 phase2completednot on this mapstarted 2015, after this paper: background citation

Decitabine Based Chemotherapy Followed by Haploidentical Lymphocyte Infusion for Elderly Patients With AML

TypeinterventionalSponsorChinese PLA General HospitalRan2015 to 2019Enrolled30ConditionsAMLArmsDecitabine 20 mg/m²/day for 5 days
NCT03467178 phase2unknown statusnot on this mapstarted 2018, after this paper: background citation

Randomized Phase II Study on Decitabine Plus Carboplatin Versus Physician's Choice Chemotherapy in Recurrent, Platinum-resistant Ovarian Cancer.

TypeinterventionalSponsorFondazione IRCCS Istituto Nazionale dei Tumori, MilanoRan2018 to 2021Enrolled119ConditionsRecurrent, Platinum-resistant Ovarian CancerArmsDecitabine, Carboplatin, Pegylated Liposomal Doxorubicin, Gemcitabine, Paclitaxel
NCT03941496 phase1 / phase2withdrawnnot on this mapstarted 2022, after this paper: background citation

Phase 1b/2a Safety and Immunogenicity of the DNMT Inhibitor Azacitidine During Anti-Tuberculosis Therapy

TypeinterventionalSponsorAndrew DinardoRan2022 to 2023Enrolled0ConditionsTuberculosis, PulmonaryArmsAzacitidine Injection
3 · Its place in the literature

Who cites it

74 citing papers in PubMed, 1 synthesis or guideline pooled it, 111 citations in OpenAlex.

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  13. Getting the right combination to break the epigenetic code.Nature reviews. Clinical oncology · 2025
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14 more citing papers are in PubMed but not listed here.

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

20 authors at 3 institutions in 2 countries.

Li-Xin WangDepartment of Hematology, Chinese PLA General Hospital, Beijing, China.
Zhen-Yang Mei
Ji-Hao Zhou
Yu-Shi Yao
Yong-Hui Li
Yi-Han Xu
Jing-Xin Li
Xiao-Ning Gao
Min-Hang Zhou
Meng-Meng Jiang
Li Gao
Yi Ding
Xue-Chun Lu
Jin-Long Shi
Xu-Feng Luo
Jia Wang
Li-Li Wang
Chunfeng Qu
Xue-Feng Bai
Li Yu
Chinese PLA General Hospital · CNThe Ohio State University · USChinese Academy of Medical Sciences & Peking Union Medical College · CN

Funding

The role of CD200 in T cell therapy of cancerR01CA138427 · NCI · OHIO STATE UNIVERSITY · PI BAI, XUE-FENG · 2009 to 2012
$981k
NCI NIH HHS R01 CA138427
6 · The paper itself

Abstract

Lack of immunogenicity of cancer cells has been considered a major reason for their failure in induction of a tumor specific T cell response. In this paper, we present evidence that decitabine (DAC), a DNA methylation inhibitor that is currently used for the treatment of myelodysplastic syndrome (MDS), acute myeloid leukemia (AML) and other malignant neoplasms, is capable of eliciting an anti-tumor cytotoxic T lymphocyte (CTL) response in mouse EL4 tumor model. C57BL/6 mice with established EL4 tumors were treated with DAC (1.0 mg/kg body weight) once daily for 5 days. We found that DAC treatment resulted in infiltration of IFN-γ producing T lymphocytes into tumors and caused tumor rejection. Depletion of CD8(+), but not CD4(+) T cells resumed tumor growth. DAC-induced CTL response appeared to be elicited by the induction of CD80 expression on tumor cells. Epigenetic evidence suggests that DAC induces CD80 expression in EL4 cells via demethylation of CpG dinucleotide sites in the promoter of CD80 gene. In addition, we also showed that a transient, low-dose DAC treatment can induce CD80 gene expression in a variety of human cancer cells. This study provides the first evidence that epigenetic modulation can induce the expression of a major T cell co-stimulatory molecule on cancer cells, which can overcome immune tolerance, and induce an efficient anti-tumor CTL response. The results have important implications in designing DAC-based cancer immunotherapy.

Indexed as

AnimalsAntimetabolites, AntineoplasticAzacitidineB7-1 AntigenCell Line, TumorCell ProliferationDecitabineDNA MethylationDose-Response Relationship, DrugFlow CytometryGene Expression Regulation, NeoplasticHumansInterferon-gammaInterleukin-2K562 CellsMiceAntimetabolites, AntineoplasticAzacitidineB7-1 AntigenDecitabineInterferon-gammaInterleukin-2

Identifiers

PMID23671644
PMCPMC3650049
OpenAlexW2022952467

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.