Evidence map›Paper›PMID 38481804›Full record

ReviewInternational journal of biological sciences2024

The scheme, and regulative mechanism of pyroptosis, ferroptosis, and necroptosis in radiation injury.

Jiaoyang Ning, Liu Chen, Yu Zeng, Gang Xiao, Wentao Tian, Qi Wu, Jiyuan Tang, Shuangshuang He, Guilong Tanzhu, Rongrong Zhou

Open access · goldAbstract readReview
In one paragraph

Review in International journal of biological sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 1 pooled it
15.9field-weighted citation impact, top 1% 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

35 citing papers in PubMed, 1 synthesis or guideline pooled it, 38 citations in OpenAlex.

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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

10 authors at 5 institutions in 2 countries.

Jiaoyang NingDepartment of Oncology, Xiangya Hospital, Central South University, Changsha, 410008, China.
Liu ChenDepartment of Oncology, Xiangya Hospital, Central South University, Changsha, 410008, China.
Yu ZengChangsha Stomatological Hospital, Hunan University of Traditional Chinese Medicine, Changsha, China.
Gang XiaoDepartment of Oncology, Xiangya Hospital, Central South University, Changsha, 410008, China.
Wentao TianDepartment of Oncology, Xiangya Hospital, Central South University, Changsha, 410008, China.
Qi WuThe Third Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Jiyuan TangDepartment of Orthopedics, Shanghai Key Laboratory for Prevention and Treatment of Bone and Joint Diseases, Shanghai Institute of Traumatology and Orthopedics, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, 197 Ruijin 2nd Road, Shanghai, 200025, China.
Shuangshuang HeDepartment of Radiation Oncology and Department of Head and Neck Oncology, Cancer Center, West China Hospital, Sichuan University, Chengdu, Sichuan, 610041, China.
Guilong TanzhuDepartment of Oncology, Xiangya Hospital, Central South University, Changsha, 410008, China.
Rongrong ZhouDepartment of Oncology, Xiangya Hospital, Central South University, Changsha, 410008, China.
Central South University · CNHunan University of Traditional Chinese Medicine · CNRuijin Hospital · CNSichuan University · CNThird Affiliated Hospital of Guangzhou Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Radiotherapy (RT) stands as the primary treatment for tumors, but it inevitably causes damage to normal cells. Consequently, radiation injury is a crucial consideration for radiation oncologists during therapy planning. Cell death including apoptosis, autophagy, pyroptosis, ferroptosis, and necroptosis play significant roles in tumor treatment. While previous studies elucidated the induction of apoptosis and autophagy by ionizing radiation (IR), recent attention has shifted to pyroptosis, ferroptosis, and necroptosis, revealing their effects induced by IR. This review aims to summarize the strategies employed by IR, either alone or in combination therapy, to induce pyroptosis, ferroptosis, and necroptosis in radiation injury. Furthermore, we explore their effects and molecular pathways, shedding light on their roles in radiation injury. Finally, we summarize the regulative agents for these three types of cell death and their mechanisms. In summary, optimizing radiation dose, dose rate, and combined treatment plans to minimize radiation damage and enhance the killing effect of RT is a key focus.

Indexed as

FerroptosisRadiation InjuriesApoptosisHumansNecroptosisPyroptosisFerroptosisNecroptosisPyroptosisRadiation injuryRegulative mechanism

Identifiers

PMID38481804
PMCPMC10929204
OpenAlexW4392830621

What OpenQuestion holds

Textmetadata
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.