Evidence map›Paper›PMID 34722507›Full record

ArticleFrontiers in cell and developmental biology2021

Iron-Dependent Autophagic Cell Death Induced by Radiation in MDA-MB-231 Breast Cancer Cells.

Shumei Ma, Xinxin Fu, Lin Liu, Yi Liu, Hao Feng, Heya Jiang, Xiaomei Liu, Rui Liu, Zhenzhen Liang, Mengke Li and 5 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

29 citing papers in PubMed, 40 citations in OpenAlex.

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  15. Iron Mediates Radiation-Induced Glioblastoma Cell Diffusion.International journal of molecular sciences · 2025
    Article
  16. Review
  17. Cell Death: Mechanisms and Potential Targets in Breast Cancer Therapy.International journal of molecular sciences · 2024
    Review
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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

15 authors at 3 institutions in 1 country.

Shumei MaSchool of Public Health and Management, Wenzhou Medical University, Wenzhou, China.
Xinxin FuSchool of Public Health and Management, Wenzhou Medical University, Wenzhou, China.
Lin LiuSchool of Public Health and Management, Wenzhou Medical University, Wenzhou, China.
Yi LiuSchool of Public Health and Management, Wenzhou Medical University, Wenzhou, China.
Hao FengSchool of Public Health and Management, Wenzhou Medical University, Wenzhou, China.
Heya JiangSchool of Public Health and Management, Wenzhou Medical University, Wenzhou, China.
Xiaomei LiuNHC Key Laboratory of Radiobiology, Jilin University, Changchun, China.
Rui LiuNHC Key Laboratory of Radiobiology, Jilin University, Changchun, China.
Zhenzhen LiangNHC Key Laboratory of Radiobiology, Jilin University, Changchun, China.
Mengke LiSchool of Public Health and Management, Wenzhou Medical University, Wenzhou, China.
Zhujun TianSchool of Public Health and Management, Wenzhou Medical University, Wenzhou, China.
Boqi HuChina-Japan Union Hospital of Jilin University, Changchun, China.
Yongheng BaiKey Laboratory of Diagnosis and Treatment of Severe Hepato-Pancreatic Diseases of Zhejiang Province, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Bing LiangSchool of Nursing, Jilin University, Changchun, China.
Xiaodong LiuSchool of Public Health and Management, Wenzhou Medical University, Wenzhou, China.
Jilin University · CNWenzhou Medical University · CNUnion Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In radiation oncology, ionizing radiation is used to kill cancer cells, in other words, the induction of different types of cell death. To investigate this cellular death and the associated iron accumulation, the transfer, release, and participation of iron after radiation treatment was analyzed. We found that radiation-induced cell death varied in different breast cancer cells and autophagy was induced in MDA-MB-231 and BT549 cells (triple negative breast cancer cell line) rather than in MCF-7 and zr-75 cells. Iron chelator deferoxamine (DFO), the autophagy inhibitor 3MA, silencing of the autophagy-related genes ATG5, and Beclin 1 could decrease radiation induced cell death in MDA-MB-231 cells, while inhibitors of apoptosis such as Z-VAD-FMK, ferroptosis inhibitor ferrostatin-1 (Fer-1), and necroptosis inhibitor Necrostatin-1 showed no change. This suggests the occurrence of autophagic cell death. Furthermore, we found that iron accumulation and iron regulatory proteins, including transferrin (Tf), transferrin receptor (CD71), and Ferritin (FTH), increased after radiation treatment, and the silencing of transferrin decreased radiation-induced cell death. In addition, radiation increased lysosomal membrane permeabilization (LMP) and the release of lysosomal iron and cathepsins, while cathepsins silencing failed to change cell viability. Radiation-induced iron accumulation increased Reactive oxygen species (ROS) generation via the Fenton reaction and increased autophagy in a time-dependent manner. DFO,

Indexed as

autophagybreast cancerironlysosome membrane permeabilization (LMP)radiationreactive oxygen species (ROS)

Identifiers

PMID34722507
PMCPMC8551752
OpenAlexW3207599194

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.