Evidence map›Paper›PMID 27671170›Full record

ArticleScientific reports2016

Combination treatment with decitabine and ionizing radiation enhances tumor cells susceptibility of T cells.

Cheol-Hun Son, Hong-Rae Lee, Eun-Kyoung Koh, Dong-Yeok Shin, Jae-Ho Bae, Kwangmo Yang, You-Soo Park

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

17 citing papers in PubMed, 27 citations in OpenAlex.

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  17. A preliminary Study on the Effect of Head and Neck Chemoradiotherapy on Systematic Immunity.Dose-response : a publication of International Hormesis Society
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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.

Cheol-Hun SonDepartment of Research Center, Dongnam Institute of Radiological &Medical Sciences, Jwadong-gil 40, Jangan-eup, Gijang-gun, Busan, 46033, Republic of Korea.
Hong-Rae LeeDepartment of Research Center, Dongnam Institute of Radiological &Medical Sciences, Jwadong-gil 40, Jangan-eup, Gijang-gun, Busan, 46033, Republic of Korea.
Eun-Kyoung KohDepartment of Research Center, Dongnam Institute of Radiological &Medical Sciences, Jwadong-gil 40, Jangan-eup, Gijang-gun, Busan, 46033, Republic of Korea.
Dong-Yeok ShinDepartment of Research Center, Dongnam Institute of Radiological &Medical Sciences, Jwadong-gil 40, Jangan-eup, Gijang-gun, Busan, 46033, Republic of Korea.
Jae-Ho BaeDepartment of Biochemistry, Pusan National University School of Medicine, Yangsan, 50612, Republic of Korea.
Kwangmo YangDepartment of Research Center, Dongnam Institute of Radiological &Medical Sciences, Jwadong-gil 40, Jangan-eup, Gijang-gun, Busan, 46033, Republic of Korea.
You-Soo ParkDepartment of Research Center, Dongnam Institute of Radiological &Medical Sciences, Jwadong-gil 40, Jangan-eup, Gijang-gun, Busan, 46033, Republic of Korea.
Dongnam Institute of Radiological & Medical Sciences · KRPusan National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Decitabine has been found to have anti-metabolic and anti-tumor activities in various tumor cells. Recently, the use of decitabine in combination with other conventional therapies reportedly resulted in improved anti-tumor activity against various tumors. Ionizing radiation (IR) is widely used as a cancer treatment. Decitabine and IR improve immunogenicity and susceptibility of tumor cells to immune cells by up-regulating the expression of various molecules such as major histocompatibility complex (MHC) class I; natural-killer group 2, member D (NKG2D) ligands; and co-stimulatory molecules. However, the effects of combining decitabine and IR therapies are largely unknown. Our results indicate that decitabine or IR treatment upregulates MHC class I, along with various co-stimulatory molecules in target tumor cells. Furthermore, decitabine and IR combination treatment further upregulates MHC class I, along with the co-stimulatory molecules, when compared to the effect of each treatment alone. Importantly, decitabine treatment further enhanced T cell-mediated cytotoxicity and release of IFN- γ against target tumor cells which is induced by IR. Interestingly, decitabine did not affect NKG2D ligand expression or NK cell-mediated cytotoxicity in target tumor cells. These observations suggest that decitabine may be used as a useful immunomodulator to sensitize tumor cells in combination with other tumor therapies.

Identifiers

PMID27671170
PMCPMC5037374
OpenAlexW2526741270

What OpenQuestion holds

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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.