Evidence map›Paper›PMID 35293589›Full record

ReviewInternational journal of molecular medicine2022

Molecular pathways associated with oxidative stress and their potential applications in radiotherapy (Review).

Rui Liu, Yan Bian, Lin Liu, Lianchang Liu, Xiaodong Liu, Shumei Ma

Open access · hybridAbstract readReview
In one paragraph

Review in International journal of molecular medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed, 2 pooled it
7.0field-weighted citation impact, top 2% 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

57 citing papers in PubMed, 2 syntheses or guidelines pooled it, 91 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Review
  5. Review
  6. Targeting glutathione metabolism for tumor radiosensitization (Review).International journal of molecular medicine · 2026
    Review
  7. Therapeutic Potential ofFood science & nutrition · 2026
    Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Radiomitigators: Breakthroughs in Post-Radiation Recovery.Antioxidants (Basel, Switzerland) · 2026
    Review
  13. Article
  14. Review
  15. Article
  16. Review
  17. Review
  18. Article
  19. Review
  20. Article
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

6 authors at 2 institutions in 1 country.

Rui LiuNHC Key Laboratory of Radiobiology, School of Public Health of Jilin University, Changchun, Jilin 130000, P.R. China.
Yan BianDepartment of Occupational and Environmental Health, School of Public Health and Management, Wenzhou Medical University, Wenzhou, Zhejiang 325000, P.R. China.
Lin LiuDepartment of Occupational and Environmental Health, School of Public Health and Management, Wenzhou Medical University, Wenzhou, Zhejiang 325000, P.R. China.
Lianchang LiuNHC Key Laboratory of Radiobiology, School of Public Health of Jilin University, Changchun, Jilin 130000, P.R. China.
Xiaodong LiuDepartment of Occupational and Environmental Health, School of Public Health and Management, Wenzhou Medical University, Wenzhou, Zhejiang 325000, P.R. China.
Shumei MaNHC Key Laboratory of Radiobiology, School of Public Health of Jilin University, Changchun, Jilin 130000, P.R. China.
Jilin University · CNWenzhou Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Radiotherapy is an essential and effective treatment modality for cancer. Excessive levels of reactive oxygen species (ROS) induced by ionizing radiation disrupt the redox homeostasis and lead to oxidative stress that may result in cell death. However, the tumor cell microenvironment is dynamic and responds to radiotherapy by activating numerous cellular signaling pathways. By scavenging excess ROS, the activity levels of the endogenous antioxidant enzymes result in radioresistance and worsen the clinical outcomes. To assess the full potential of radiotherapy, it is essential to explore the underlying mechanisms of oxidative stress in radiotherapy for potential target identification. The present review article summarized recent data demonstrating nuclear factor‑erythroid factor 2‑related factor 2 (Nrf2) as a powerful transcription factor and one of the major cellular defense mechanisms that protect against oxidative stress in response to radiotherapy; the glutathione (GSH) and thioredoxin (Trx) systems complement each other and are effective antioxidant mechanisms associated with the protection of cancer cells from radiation damage. In addition, it is suggested that dual targeting to inhibit GSH and Trx enzymes may be a potential strategy for the development of radiosensitive and radioprotective drugs.

Indexed as

GlutathioneOxidative StressAntioxidantsOxidation-ReductionReactive Oxygen SpeciesAntioxidantsGlutathioneReactive Oxygen Speciesglutathione metabolismoxidative stressradiosensitivityradiotherapythioredoxin

Identifiers

PMID35293589
PMCPMC8989428
OpenAlexW4220717410

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.