Evidence map›Paper›PMID 38368473›Full record

ArticleCommunications biology2024

Phenolic compounds induce ferroptosis-like death by promoting hydroxyl radical generation in the Fenton reaction.

Xinyue Sui, Jichao Wang, Zhiqiang Zhao, Bin Liu, Miaomiao Liu, Min Liu, Cong Shi, Xinjun Feng, Yingxin Fu, Dayong Shi and 4 more

Open access · goldAbstract read
In one paragraph

Article in Communications biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
10.8field-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

27 citing papers in PubMed, 46 citations in OpenAlex.

  1. Science advances · 2026
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  14. Revolutionizing antibiotic therapy: Polymyxin B and FeJournal of pharmaceutical analysis · 2025
    Article
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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

14 authors at 4 institutions in 1 country.

Xinyue SuiState Key Laboratory of Microbial Technology and Institute of Microbial Technology, Shandong University, Qingdao, China.
Jichao WangState Key Laboratory of Microbial Technology and Institute of Microbial Technology, Shandong University, Qingdao, China.
Zhiqiang ZhaoCAS Key Lab of Biobased Materials, Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of Sciences, Qingdao, China.
Bin LiuTEDA Institute of Biological Sciences and Biotechnology, Nankai University, Tianjin, China.
Miaomiao LiuTEDA Institute of Biological Sciences and Biotechnology, Nankai University, Tianjin, China.
Min LiuState Key Laboratory of Microbial Technology and Institute of Microbial Technology, Shandong University, Qingdao, China.
Cong ShiState Key Laboratory of Microbial Technology and Institute of Microbial Technology, Shandong University, Qingdao, China.
Xinjun FengCAS Key Lab of Biobased Materials, Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of Sciences, Qingdao, China.
Yingxin FuState Key Laboratory of Microbial Technology and Institute of Microbial Technology, Shandong University, Qingdao, China.
Dayong ShiState Key Laboratory of Microbial Technology and Institute of Microbial Technology, Shandong University, Qingdao, China.
Shengying LiState Key Laboratory of Microbial Technology and Institute of Microbial Technology, Shandong University, Qingdao, China.ORCID 0000-0002-5244-870X
Qingsheng QiState Key Laboratory of Microbial Technology and Institute of Microbial Technology, Shandong University, Qingdao, China.ORCID 0000-0001-9015-4561
Mo XianCAS Key Lab of Biobased Materials, Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of Sciences, Qingdao, China.
Guang ZhaoState Key Laboratory of Microbial Technology and Institute of Microbial Technology, Shandong University, Qingdao, China. zhaoguang@sdu.edu.cn.ORCID 0000-0003-0002-5972
Shandong University · CNChinese Academy of Sciences · CNNankai University · CNQingdao University of Science and Technology · CN

Funding

National Natural Science Foundation of China (National Science Foundation of China) 32170085
6 · The paper itself

Abstract

Phenolic compounds are industrially versatile chemicals, also the most ubiquitous pollutants. Recently, biosynthesis and biodegradation of phenols has attracted increasing attention, while phenols' toxicity is a major issue. Here, we evolved phloroglucinol-tolerant Escherichia coli strains via adaptive evolution, and three mutations (ΔsodB, ΔclpX and fetAB overexpression) prove of great assistance in the tolerance improvement. We discover that phloroglucinol complexes with iron and promotes the generation of hydroxyl radicals in Fenton reaction, which leads to reducing power depletion, lipid peroxidation, and ferroptosis-like cell death of E. coli. Besides phloroglucinol, various phenols can trigger ferroptosis-like death in diverse organisms, from bacteria to mammalian cells. Furthermore, repressing this ferroptosis-like death improves phloroglucinol production and phenol degradation by corresponding strains respectively, showing great application potential in microbial degradation or production of desired phenolic compounds, and phloroglucinol-induced ferroptosis suppresses tumor growth in mice, indicating phloroglucinol as a promising drug for cancer treatment.

Indexed as

FerroptosisHydroxyl RadicalAnimalsEscherichia coliMammalsMicePhenolsPhloroglucinolHydroxyl RadicalPhenolsPhloroglucinol

Identifiers

PMID38368473
PMCPMC10874397
OpenAlexW4391896678

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.