Evidence map›Paper›PMID 36627132›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2023

Tryptophan Metabolism Acts as a New Anti-Ferroptotic Pathway to Mediate Tumor Growth.

Dong Liu, Chun-Hui Liang, Bin Huang, Xiao Zhuang, Weiwei Cui, Li Yang, Yinghong Yang, Yudan Zhang, Xiaolong Fu, Xiaoju Zhang and 6 more

Open access · goldAbstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 96 papers.

0numbers the graph read from it
0cells of the map it votes in
96citing papers in PubMed
37.0field-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

96 citing papers in PubMed, 139 citations in OpenAlex.

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36 more citing papers are in PubMed but not listed here.

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

16 authors at 7 institutions in 2 countries.

Dong LiuDepartment of Cell Biology, School of Basic Medical Sciences, Cheeloo College of Medicine, Shandong University, Jinan, Shandong, 250012, China.
Chun-Hui LiangDepartment of Cell Biology, School of Basic Medical Sciences, Cheeloo College of Medicine, Shandong University, Jinan, Shandong, 250012, China.
Bin HuangInstitute for Cancer Research, Shenzhen Bay Laboratory, Shenzhen, 518107, China.
Xiao ZhuangDepartment of Cell Biology, School of Basic Medical Sciences, Cheeloo College of Medicine, Shandong University, Jinan, Shandong, 250012, China.
Weiwei CuiDepartment of Cell Biology, School of Basic Medical Sciences, Cheeloo College of Medicine, Shandong University, Jinan, Shandong, 250012, China.
Li YangDepartment of Respiratory and Critical Care Medicine, Zhengzhou University People's Hospital, Henan Provincial People's Hospital, Zhengzhou University, Zhengzhou, Henan, 450000, China.
Yinghong YangDepartment of Cell Biology, School of Basic Medical Sciences, Cheeloo College of Medicine, Shandong University, Jinan, Shandong, 250012, China.
Yudan ZhangDepartment of Cell Biology, School of Basic Medical Sciences, Cheeloo College of Medicine, Shandong University, Jinan, Shandong, 250012, China.
Xiaolong FuState Key Laboratory of Bioelectronics, Department of Otolaryngology Head and Neck Surgery, Zhongda Hospital, School of Life Sciences and Technology, Advanced Institute for Life and Health, Jiangsu Province High-Tech Key Laboratory for Bio-Medical Research, Southeast University, Nanjing, 210096, China.
Xiaoju ZhangDepartment of Respiratory and Critical Care Medicine, Zhengzhou University People's Hospital, Henan Provincial People's Hospital, Zhengzhou University, Zhengzhou, Henan, 450000, China.
Lutao DuDepartment of Clinical Laboratory, The Second Hospital of Shandong University, Jinan, Shandong, 250033, China.
Wei GuInstitute for Cancer Genetics, and Department of Pathology and Cell Biology, Herbert Irving Comprehensive Cancer Center, College of Physicians and Surgeons, Columbia University, 1130 Nicholas Ave, New York, NY, 10032, USA.
Xiangdong WangDepartment of Cell Biology, School of Basic Medical Sciences, Cheeloo College of Medicine, Shandong University, Jinan, Shandong, 250012, China.ORCID 0000-0002-8827-3470
Chengqian YinInstitute for Cancer Research, Shenzhen Bay Laboratory, Shenzhen, 518107, China.
Renjie ChaiState Key Laboratory of Bioelectronics, Department of Otolaryngology Head and Neck Surgery, Zhongda Hospital, School of Life Sciences and Technology, Advanced Institute for Life and Health, Jiangsu Province High-Tech Key Laboratory for Bio-Medical Research, Southeast University, Nanjing, 210096, China.
Bo ChuDepartment of Cell Biology, School of Basic Medical Sciences, Cheeloo College of Medicine, Shandong University, Jinan, Shandong, 250012, China.ORCID 0000-0001-9754-2743
Shandong University · CNShenzhen Bay Laboratory · CNZhengzhou University · CNCancer Genetics (United States) · USSecond Hospital of Shandong University · CNState Key Laboratory of Digital Medical EngineeringUniversity of Electronic Science and Technology of China · CN

Funding

GuangDong Basic and Applied Basic Research Foundation 2020A1515110857National Key R&D Program of China 2020YFA0112503National Key R&D Program of China 2021YFA1101300National Natural Science Foundation of China 32000515National Natural Science Foundation of China 3210050537National Natural Science Foundation of China 81970882National Natural Science Foundation of China 82030029Natural Science Foundation from Jiangsu Province BE2019711Natural Science Foundation of Shandong Province ZR2020QC074Open Research Fund of State Key Laboratory of Genetic Engineering, Fudan University SKLGE-2109Science and Technology Department of Sichuan Province 2021YFS0371Shandong UniversityShenzhen Bay Laboratory SZBL2021080601004Shenzhen Fundamental Research Program JCYJ20190814093401920Shenzhen Fundamental Research Program JCYJ20210324125608022Strategic Priority Research Program of the Chinese Academy of Science XDA16010303Taishan Scholars Program TSQN201909030
6 · The paper itself

Abstract

Emerging evidence reveals that amino acid metabolism plays an important role in ferroptotic cell death. The conversion of methionine to cysteine is well known to protect tumour cells from ferroptosis upon cysteine starvation through transamination. However, whether amino acids-produced metabolites participate in ferroptosis independent of the cysteine pathway is largely unknown. Here, the authors show that the tryptophan metabolites serotonin (5-HT) and 3-hydroxyanthranilic acid (3-HA) remarkably facilitate tumour cells to escape from ferroptosis distinct from cysteine-mediated ferroptosis inhibition. Mechanistically, both 5-HT and 3-HA act as potent radical trapping antioxidants (RTA) to eliminate lipid peroxidation, thereby inhibiting ferroptotic cell death. Monoamine oxidase A (MAOA) markedly abrogates the protective effect of 5-HT via degrading 5-HT. Deficiency of MAOA renders cancer cells resistant to ferroptosis upon 5-HT treatment. Kynureninase (KYNU), which is essential for 3-HA production, confers cells resistant to ferroptotic cell death, whereas 3-hydroxyanthranilate 3,4-dioxygenase (HAAO) significantly blocks 3-HA mediated ferroptosis inhibition by consuming 3-HA. In addition, the expression level of HAAO is positively correlated with lipid peroxidation and clinical outcome. Together, the findings demonstrate that tryptophan metabolism works as a new anti-ferroptotic pathway to promote tumour growth, and targeting this pathway will be a promising therapeutic approach for cancer treatment.

Indexed as

NeoplasmsTryptophanCysteineHumansLipid PeroxidationSerotoninCysteineSerotoninTryptophan3-HA3-hydroxyanthranilate 3,4-dioxygenase (HAAO)5-HTferroptosiskynureninase (KYNUmonoamine oxidase A (MAOA)tryptophan

Identifiers

PMID36627132
PMCPMC9951368
OpenAlexW4315471136

What OpenQuestion holds

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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.