Evidence map›Paper›PMID 34196706›Full record

ArticleJournal of radiation research2021

High linear energy transfer carbon-ion irradiation upregulates PD-L1 expression more significantly than X-rays in human osteosarcoma U2OS cells.

Tiara Bunga Mayang Permata, Hiro Sato, Wenchao Gu, Sangeeta Kakoti, Yuki Uchihara, Yukihiko Yoshimatsu, Itaru Sato, Reona Kato, Motohiro Yamauchi, Keiji Suzuki and 6 more

Open access · goldAbstract read
In one paragraph

Article in Journal of radiation research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.1field-weighted citation impact, top 10% 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

22 citing papers in PubMed, 31 citations in OpenAlex.

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  11. Key molecular DNA damage responses of human cells to radiation.Frontiers in cell and developmental biology · 2024
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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

16 authors at 5 institutions in 2 countries.

Tiara Bunga Mayang PermataDepartment of Radiation Oncology, Gunma University, Maebashi, Gunma, 371-8511, Japan.
Hiro SatoDepartment of Radiation Oncology, Gunma University, Maebashi, Gunma, 371-8511, Japan.
Wenchao GuGunma University Initiative for Advanced Research (GIAR), Gunma University, Maebashi, Gunma, 371-8511, Japan.
Sangeeta KakotiDepartment of Radiation Oncology, Gunma University, Maebashi, Gunma, 371-8511, Japan.
Yuki UchiharaGunma University Initiative for Advanced Research (GIAR), Gunma University, Maebashi, Gunma, 371-8511, Japan.
Yukihiko YoshimatsuGunma University Initiative for Advanced Research (GIAR), Gunma University, Maebashi, Gunma, 371-8511, Japan.
Itaru SatoGunma University Initiative for Advanced Research (GIAR), Gunma University, Maebashi, Gunma, 371-8511, Japan.
Reona KatoLaboratory of Molecular Radiology, Center for Disease Biology and Integrative Medicine, Graduate School of Medicine, The University of Tokyo, Bunkyo-ku, Tokyo, 113-8655, Japan.
Motohiro YamauchiDepartment of Radiation Biology and Protection, Atomic Bomb Disease Institute, Nagasaki University, Nagasaki, 852-8523, Japan.
Keiji SuzukiDepartment of Radiation Medical Science, Atomic Bomb Disease Institute, Nagasaki University, Nagasaki, 852-8523, Japan.
Takahiro OikeDepartment of Radiation Oncology, Gunma University, Maebashi, Gunma, 371-8511, Japan.
Yoshito TsushimaGunma University Initiative for Advanced Research (GIAR), Gunma University, Maebashi, Gunma, 371-8511, Japan.
Soehartati GondhowiardjoDepartment of Radiation Oncology, Faculty of Medicine Universitas Indonesia - Dr. Cipto Mangunkusumo Hospital, Jakarta, 10430, Indonesia.
Tatsuya OhnoDepartment of Radiation Oncology, Gunma University, Maebashi, Gunma, 371-8511, Japan.
Takaaki YasuharaLaboratory of Molecular Radiology, Center for Disease Biology and Integrative Medicine, Graduate School of Medicine, The University of Tokyo, Bunkyo-ku, Tokyo, 113-8655, Japan.
Atsushi ShibataGunma University Initiative for Advanced Research (GIAR), Gunma University, Maebashi, Gunma, 371-8511, Japan.
Gunma University · JPNagasaki University · JPRumah Sakit Umum Pusat Nasional Dr. Cipto Mangunkusumo · IDThe University of Tokyo · JPGunma University Hospital · JP

Funding

Japan Society for the Promotion of Science JP19K08195
6 · The paper itself

Abstract

Programmed death ligand 1 (PD-L1) expression on the surface of cancer cells affects the efficacy of anti-PD-1/PD-L1 immune checkpoint therapy. However, the mechanism underlying PD-L1 expression in cancer cells is not fully understood, particularly after ionizing radiation (IR). Here, we examined the impact of high linear energy transfer (LET) carbon-ion irradiation on the expression of PD-L1 in human osteosarcoma U2OS cells. We found that the upregulation of PD-L1 expression after high LET carbon-ion irradiation was greater than that induced by X-rays at the same physical and relative biological effectiveness (RBE) dose, and that the upregulation of PD-L1 induced by high LET carbon-ion irradiation was predominantly dependent on ataxia telangiectasia and Rad3-related (ATR) kinase activity. Moreover, we showed that the downstream signaling, e.g. STAT1 phosphorylation and IRF1 expression, was upregulated to a greater extent after high LET carbon-ion irradiation than X-rays, and that IRF1 upregulation was also ATR dependent. Finally, to visualize PD-L1 molecules on the cell surface in 3D, we applied immunofluorescence-based super-resolution imaging. The three-dimensional structured illumination microscopy (3D-SIM) analyses revealed substantial increases in the number of presented PD-L1 molecules on the cell surface after high LET carbon-ion irradiation compared with X-ray irradiation.

Indexed as

Heavy Ion RadiotherapyAtaxia Telangiectasia Mutated ProteinsB7-H1 AntigenBone NeoplasmsCell Line, TumorGene Expression Regulation, NeoplasticHumansImaging, Three-DimensionalInterferon Regulatory Factor-1Linear Energy TransferMorpholinesNeoplasm ProteinsOsteosarcomaPhosphorylationProtein Processing, Post-TranslationalPyrazines2-morpholin-4-yl-6-thianthren-1-yl-pyran-4-one3-amino-6-(4-(methylsulfonyl)phenyl)-N-phenylpyrazine-2-carboxamideAtaxia Telangiectasia Mutated ProteinsATM protein, humanATR protein, humanB7-H1 AntigenCD274 protein, humanInterferon Regulatory Factor-1IRF1 protein, humanMorpholinesNeoplasm ProteinsPyrazinesPyronesRNA, MessengerRNA, NeoplasmSTAT1 protein, humanSTAT1 Transcription FactorSulfonesanti-PD-1/PD-L1 therapyDNA damage responsehigh linear energy transfer (LET) carbon-ion therapyPD-L1 expression

Identifiers

PMID34196706
PMCPMC8438258
OpenAlexW3177056866

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.