Evidence map›Paper›PMID 38839752›Full record

ArticleNature communications2024

FBXO7 ubiquitinates PRMT1 to suppress serine synthesis and tumor growth in hepatocellular carcinoma.

Li Luo, Xingyun Wu, Jiawu Fan, Lixia Dong, Mao Wang, Yan Zeng, Sijia Li, Wenyong Yang, Jingwen Jiang, Kui Wang

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
–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

53 citing papers in PubMed.

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  14. PHGDH is a targetable driver of PDAC progression.bioRxiv : the preprint server for biology · 2026
    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

10 authors.

Li Luo *West China School of Basic Medical Sciences & Forensic Medicine, State Key Laboratory of Biotherapy, West China Hospital, West China School of Public Health and West China Fourth Hospital, Sichuan University, 610041, Chengdu, P. R. China.
Xingyun Wu *West China School of Basic Medical Sciences & Forensic Medicine, State Key Laboratory of Biotherapy, West China Hospital, West China School of Public Health and West China Fourth Hospital, Sichuan University, 610041, Chengdu, P. R. China.
Jiawu Fan *West China School of Basic Medical Sciences & Forensic Medicine, State Key Laboratory of Biotherapy, West China Hospital, West China School of Public Health and West China Fourth Hospital, Sichuan University, 610041, Chengdu, P. R. China.
Lixia DongWest China School of Basic Medical Sciences & Forensic Medicine, State Key Laboratory of Biotherapy, West China Hospital, West China School of Public Health and West China Fourth Hospital, Sichuan University, 610041, Chengdu, P. R. China.
Mao WangWest China School of Basic Medical Sciences & Forensic Medicine, State Key Laboratory of Biotherapy, West China Hospital, West China School of Public Health and West China Fourth Hospital, Sichuan University, 610041, Chengdu, P. R. China.
Yan ZengWest China School of Basic Medical Sciences & Forensic Medicine, State Key Laboratory of Biotherapy, West China Hospital, West China School of Public Health and West China Fourth Hospital, Sichuan University, 610041, Chengdu, P. R. China.
Sijia LiWest China School of Basic Medical Sciences & Forensic Medicine, State Key Laboratory of Biotherapy, West China Hospital, West China School of Public Health and West China Fourth Hospital, Sichuan University, 610041, Chengdu, P. R. China.
Wenyong YangDepartment of Neurosurgery, Medical Research Center, The Third People's Hospital of Chengdu, The Affiliated Hospital of Southwest Jiaotong University, The Second Chengdu Hospital Affiliated to Chongqing Medical University, 610014, Chengdu, P.R. China.
Jingwen JiangWest China School of Basic Medical Sciences & Forensic Medicine, State Key Laboratory of Biotherapy, West China Hospital, West China School of Public Health and West China Fourth Hospital, Sichuan University, 610041, Chengdu, P. R. China. jjwcn@foxmail.com.ORCID http://orcid.org/0009-0006-9768-0314
Kui WangWest China School of Basic Medical Sciences & Forensic Medicine, State Key Laboratory of Biotherapy, West China Hospital, West China School of Public Health and West China Fourth Hospital, Sichuan University, 610041, Chengdu, P. R. China. kuiwang@scu.edu.cn.ORCID http://orcid.org/0000-0003-3503-1563

Funding

National Natural Science Foundation of China (National Science Foundation of China) 82002963National Natural Science Foundation of China (National Science Foundation of China) 82003098National Natural Science Foundation of China (National Science Foundation of China) 82073081National Natural Science Foundation of China (National Science Foundation of China) 82303238National Natural Science Foundation of China (National Science Foundation of China) 82373122
6 · The paper itself

Abstract

Cancer cells are often addicted to serine synthesis to support growth. How serine synthesis is regulated in cancer is not well understood. We recently demonstrated protein arginine methyltransferase 1 (PRMT1) is upregulated in hepatocellular carcinoma (HCC) to methylate and activate phosphoglycerate dehydrogenase (PHGDH), thereby promoting serine synthesis. However, the mechanisms underlying PRMT1 upregulation and regulation of PRMT1-PHGDH axis remain unclear. Here, we show the E3 ubiquitin ligase F-box-only protein 7 (FBXO7) inhibits serine synthesis in HCC by binding PRMT1, inducing lysine 37 ubiquitination, and promoting proteosomal degradation of PRMT1. FBXO7-mediated PRMT1 downregulation cripples PHGDH arginine methylation and activation, resulting in impaired serine synthesis, accumulation of reactive oxygen species (ROS), and inhibition of HCC cell growth. Notably, FBXO7 is significantly downregulated in human HCC tissues, and inversely associated with PRMT1 protein and PHGDH methylation level. Overall, our study provides mechanistic insights into the regulation of cancer serine synthesis by FBXO7-PRMT1-PHGDH axis, and will facilitate the development of serine-targeting strategies for cancer therapy.

Indexed as

Carcinoma, HepatocellularF-Box ProteinsLiver NeoplasmsPhosphoglycerate DehydrogenaseProtein-Arginine N-MethyltransferasesSerineUbiquitinationAnimalsCell Line, TumorCell ProliferationFemaleGene Expression Regulation, NeoplasticHEK293 CellsHep G2 CellsHumansMaleF-Box ProteinsFBXO7 protein, humanPhosphoglycerate DehydrogenasePRMT1 protein, humanProtein-Arginine N-MethyltransferasesRepressor ProteinsSerine

Identifiers

PMID38839752
PMCPMC11153525

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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.