Evidence map›Paper›PMID 36060242›Full record

ReviewFrontiers in molecular biosciences2022

Emerging role of ferroptosis in glioblastoma: Therapeutic opportunities and challenges.

Shenghua Zhuo, Guiying He, Taixue Chen, Xiang Li, Yunheng Liang, Wenkai Wu, Lingxiao Weng, Jigao Feng, Zhenzhong Gao, Kun Yang

Abstract readReview
In one paragraph

Review in Frontiers in molecular biosciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

31 citing papers in PubMed, 1 synthesis or guideline pooled it.

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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.

Shenghua ZhuoDepartment of Neurosurgery, First Affiliated Hospital of Hainan Medical University, Haikou, China.
Guiying HeDepartment of Neurology, Shenzhen Sixth People's Hospital, Huazhong University of Science and Technology Union Shenzhen Hospital, Shenzhen, China.
Taixue ChenDepartment of Neurosurgery, First Affiliated Hospital of Hainan Medical University, Haikou, China.
Xiang LiDepartment of Neurology, Shenzhen Sixth People's Hospital, Huazhong University of Science and Technology Union Shenzhen Hospital, Shenzhen, China.
Yunheng LiangDepartment of Neurosurgery, First Affiliated Hospital of Hainan Medical University, Haikou, China.
Wenkai WuDepartment of Neurosurgery, First Affiliated Hospital of Hainan Medical University, Haikou, China.
Lingxiao WengDepartment of Neurosurgery, First Affiliated Hospital of Hainan Medical University, Haikou, China.
Jigao FengDepartment of Neurosurgery, Second Affiliated Hospital of Hainan Medical University, Haikou, China.
Zhenzhong GaoDepartment of Neurosurgery, First Affiliated Hospital of Hainan Medical University, Haikou, China.
Kun YangDepartment of Neurosurgery, First Affiliated Hospital of Hainan Medical University, Haikou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma (GBM) is the most common malignant craniocerebral tumor. The treatment of this cancer is difficult due to its high heterogeneity and immunosuppressive microenvironment. Ferroptosis is a newly found non-apoptotic regulatory cell death process that plays a vital role in a variety of brain diseases, including cerebral hemorrhage, neurodegenerative diseases, and primary or metastatic brain tumors. Recent studies have shown that targeting ferroptosis can be an effective strategy to overcome resistance to tumor therapy and immune escape mechanisms. This suggests that combining ferroptosis-based therapies with other treatments may be an effective strategy to improve the treatment of GBM. Here, we critically reviewed existing studies on the effect of ferroptosis on GBM therapies such as chemotherapy, radiotherapy, immunotherapy, and targeted therapy. In particular, this review discussed the potential of ferroptosis inducers to reverse drug resistance and enhance the sensitivity of conventional cancer therapy in combination with ferroptosis. Finally, we highlighted the therapeutic opportunities and challenges facing the clinical application of ferroptosis-based therapies in GBM. The data generated here provide new insights and directions for future research on the significance of ferroptosis-based therapies in GBM.

Indexed as

cancer therapyferroptosisglioblastomaimmunotherapytherapy resistance

Identifiers

PMID36060242
PMCPMC9428609

What OpenQuestion holds

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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.