Evidence map›Paper›PMID 35668934›Full record

ReviewFrontiers in pharmacology2022

Ferroptosis and Tumor Drug Resistance: Current Status and Major Challenges.

Zhenyu Nie, Mei Chen, Yuanhui Gao, Denggao Huang, Hui Cao, Yanling Peng, Na Guo, Fei Wang, Shufang Zhang

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in pharmacology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed, 2 pooled it
8.4field-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

51 citing papers in PubMed, 2 syntheses or guidelines pooled it, 62 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. Article
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  11. Review
  12. Article
  13. Ferroptosis-centered strategies: redefining therapeutic resistance & adaptation in modern oncology.Apoptosis : an international journal on programmed cell death · 2026
    Review
  14. Review
  15. Membrane Stress and Ferroptosis: Lipid Dynamics in Cancer.International journal of molecular sciences · 2026
    Review
  16. Article
  17. Review
  18. Article
  19. ACTG1 mediates cisplatin resistance in NSCLC through induction of mitochondrial fragmentation.Apoptosis : an international journal on programmed cell death · 2025
    Article
  20. 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

9 authors at 3 institutions in 1 country.

Zhenyu NieCentral Laboratory, Affiliated Haikou Hospital of Xiangya Medical College, Central South University, Haikou, China.
Mei ChenCentral Laboratory, Affiliated Haikou Hospital of Xiangya Medical College, Central South University, Haikou, China.
Yuanhui GaoCentral Laboratory, Affiliated Haikou Hospital of Xiangya Medical College, Central South University, Haikou, China.
Denggao HuangCentral Laboratory, Affiliated Haikou Hospital of Xiangya Medical College, Central South University, Haikou, China.
Hui CaoCentral Laboratory, Affiliated Haikou Hospital of Xiangya Medical College, Central South University, Haikou, China.
Yanling PengCentral Laboratory, Affiliated Haikou Hospital of Xiangya Medical College, Central South University, Haikou, China.
Na GuoCentral Laboratory, Affiliated Haikou Hospital of Xiangya Medical College, Central South University, Haikou, China.
Fei WangDepartment of Urology, Hainan General Hospital, Affiliated Hainan Hospital of Hainan Medical University, Haikou, China.
Shufang ZhangCentral Laboratory, Affiliated Haikou Hospital of Xiangya Medical College, Central South University, Haikou, China.
Central South University · CNHainan Medical University · CNHainan General Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ferroptosis is a novel type of regulated cell death, whose unique metabolic characteristics are commonly used to evaluate the conditions of various diseases especially in tumors. Accumulating evidence supports that ferroptosis can regulate tumor development, metastasis, and therapeutic responses. Considering to the important role of chemotherapy in tumor treatment, drug resistance has become the most serious challenge. Revealing the molecular mechanism of ferroptosis is expected to solve tumor drug resistance and find new therapies to treat cancers. In this review, we discuss the relationship between ferroptosis and tumor drug resistance, summarize the abnormal ferroptosis in tissues of different cancer types and current research progress and challenges in overcoming treatment resistance, and explore the concept of targeting ferroptosis to improve tumor treatment outcomes.

Indexed as

chemotherapyferroptosisimmunotherapytarget therapytumor drug resistance

Identifiers

PMID35668934
PMCPMC9163417
OpenAlexW4280534108

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.