Evidence map›Paper›PMID 36389749›Full record

ArticleFrontiers in immunology2022

Single-cell mechanistic studies of radiation-mediated bystander effects.

Xueqiong Han, Yixuan Chen, Nan Zhang, Chengyu Huang, Guangyao He, Ting Li, Mengxin Wei, Qiong Song, Shaowen Mo, Yufeng Lv

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
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

10 authors at 1 institution in 1 country.

Xueqiong HanDepartment of Oncology, The Fifth Affiliated Hospital of Guangxi Medical University, Nanning, China.
Yixuan ChenDepartment of Basic Science, YuanDong International Academy Of Life Sciences, Hong Kong, China.
Nan ZhangDepartment of Basic Science, YuanDong International Academy Of Life Sciences, Hong Kong, China.
Chengyu HuangDepartment of Basic Science, YuanDong International Academy Of Life Sciences, Hong Kong, China.
Guangyao HeDepartment of Otolaryngology-Head and Neck Surgery, The First Hospital of Guangxi Medical University, Nanning, China.
Ting LiDepartment of Basic Science, YuanDong International Academy Of Life Sciences, Hong Kong, China.
Mengxin WeiDepartment of Basic Science, YuanDong International Academy Of Life Sciences, Hong Kong, China.
Qiong SongDepartment of Basic Science, YuanDong International Academy Of Life Sciences, Hong Kong, China.
Shaowen MoDepartment of Basic Science, YuanDong International Academy Of Life Sciences, Hong Kong, China.
Yufeng LvDepartment of Oncology, Foresea Life Insurance Guangxi Hospital, Nanning, China.
Guangxi Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ionizing radiation (IR) has been widely used in the diagnosis and treatment of clinical diseases, with radiation therapy (RT) being particularly rapid, but it can induce "bystander effects" that lead to biological responses in non-target cells after their neighboring cells have been irradiated. To help clarify how radiotherapy induces these effects, To help clarify how radiotherapy induces these effects, we analyzed single-cell RNA sequencing data from irradiated intestinal tissues on day 1 (T1 state), day 3 (T3 state), day 7 (T7 state), and day 14 (T14 state) after irradiation, as well as from healthy intestinal tissues (T0 state), to reveal the cellular level, molecular level, and involvement of different time irradiated mouse intestinal tissues in biological signaling pathways. In addition, changes in immune cell subpopulations and myeloid cell subpopulations after different radiation times were further explored, and gene regulatory networks (GRNs) of these cell subpopulations were constructed. Cellular communication between radiation-specific immune cells was explored by cell-to-cell communication events. The results suggest that radiotherapy trigger changes in immune cell subsets, which then reprogram the immune ecosystem and mediate systemic bystander effects. These radiation-specific immune cells participate in a wide range of cell-to-cell communication events. In particular, radiation-specific CD8+T cells appear to be at the core of communication and appear to persist in the body after recovery from radiotherapy, with enrichment analysis showing that radiation-specific CD8+ T cells are associated with ferroptosis. Thus, radiation-specific CD8+ T cells may be involved in cellular ferroptosis-mediated adverse effects caused by RT.

Indexed as

Bystander EffectRadiation InjuriesAnimalsMiceRadiation, IonizingSignal Transductionbystander effectcell communicationferroptosisradiotherapyreprogramming

Identifiers

PMID36389749
PMCPMC9640915
OpenAlexW4307372431

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.