Evidence map›Paper›PMID 31819189›Full record

ArticleBritish journal of cancer2020

MFN1-dependent alteration of mitochondrial dynamics drives hepatocellular carcinoma metastasis by glucose metabolic reprogramming.

Ze Zhang, Tian-En Li, Mo Chen, Da Xu, Ying Zhu, Bei-Yuan Hu, Zhi-Fei Lin, Jun-Jie Pan, Xuan Wang, Chao Wu and 6 more

Open access · hybridAbstract read
In one paragraph

Article in British journal of cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 111 papers.

0numbers the graph read from it
0cells of the map it votes in
111citing papers in PubMed
11.1field-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

111 citing papers in PubMed, 229 citations in OpenAlex.

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  11. Mitochondrial Calcium Signaling in Hepatocyte Health and Disease.Cold Spring Harbor perspectives in biology · 2026
    Review
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  20. Metabolic adaptations of brain metastasis.Nature reviews. Cancer · 2025
    Review

51 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 4 institutions in 1 country.

Ze Zhang *Department of General Surgery, Huashan Hospital, Fudan University, Shanghai, China.
Tian-En Li *Department of General Surgery, Huashan Hospital, Fudan University, Shanghai, China.
Mo Chen *Department of General Surgery, Huashan Hospital, Fudan University, Shanghai, China.
Da XuDepartment of General Surgery, Huashan Hospital, Fudan University, Shanghai, China.
Ying ZhuDepartment of General Surgery, Huashan Hospital, Fudan University, Shanghai, China.
Bei-Yuan HuDepartment of General Surgery, Huashan Hospital, Fudan University, Shanghai, China.
Zhi-Fei LinDepartment of General Surgery, Huashan Hospital, Fudan University, Shanghai, China.
Jun-Jie PanDepartment of General Surgery, Huashan Hospital, Fudan University, Shanghai, China.
Xuan WangDepartment of General Surgery, Huashan Hospital, Fudan University, Shanghai, China.
Chao WuDepartment of General Surgery, Huashan Hospital, Fudan University, Shanghai, China.
Yan ZhengDepartment of General Surgery, Huashan Hospital, Fudan University, Shanghai, China.
Lu LuDepartment of General Surgery, Huashan Hospital, Fudan University, Shanghai, China.
Hu-Liang JiaDepartment of General Surgery, Huashan Hospital, Fudan University, Shanghai, China.
Song GaoState Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-sen University Cancer Center, Guangzhou, China. gaosong@sysucc.org.cn.
Qiong-Zhu DongDepartment of General Surgery, Huashan Hospital, Fudan University, Shanghai, China. qzhdong@fudan.edu.cn.
Lun-Xiu QinDepartment of General Surgery, Huashan Hospital, Fudan University, Shanghai, China. qinlx@fudan.edu.cn.
Fudan University · CNHuashan Hospital · CNFudan University Shanghai Cancer Center · CNSun Yat-sen University · CN

Funding

National Natural Science Foundation of China (National Science Foundation of China) 31722016National Natural Science Foundation of China (National Science Foundation of China) 81672820National Natural Science Foundation of China (National Science Foundation of China) 81930074
6 · The paper itself

Abstract

backgroundMitochondrial dynamics plays an important role in tumour progression. However, how these dynamics integrate tumour metabolism in hepatocellular carcinoma (HCC) metastasis is still unclear.

methodsThe mitochondrial fusion protein mitofusin-1 (MFN1) expression and its prognostic value are detected in HCC. The effects and underlying mechanisms of MFN1 on HCC metastasis and metabolic reprogramming are analysed both in vitro and in vivo.

resultsMitochondrial dynamics, represented by constant fission and fusion, are found to be associated with HCC metastasis. High metastatic HCC displays excessive mitochondrial fission. Among genes involved in mitochondrial dynamics, MFN1 is identified as a leading downregulated candidate that is closely associated with HCC metastasis and poor prognosis. While promoting mitochondrial fusion, MFN1 inhibits cell proliferation, invasion and migration capacity both in vitro and in vivo. Mechanistically, disruption of mitochondrial dynamics by depletion of MFN1 triggers the epithelial-to-mesenchymal transition (EMT) of HCC. Moreover, MFN1 modulates HCC metastasis by metabolic shift from aerobic glycolysis to oxidative phosphorylation. Treatment with glycolytic inhibitor 2-Deoxy-D-glucose (2-DG) significantly suppresses the effects induced by depletion of MFN1.

conclusionsOur results reveal a critical involvement of mitochondrial dynamics in HCC metastasis via modulating glucose metabolic reprogramming. MFN1 may serve as a novel potential therapeutic target for HCC.

Indexed as

Carcinoma, HepatocellularCell ProliferationDeoxyglucoseEpithelial-Mesenchymal TransitionGene Expression Regulation, NeoplasticGlucoseGlycolysisGTP PhosphohydrolasesHumansLiver NeoplasmsMitochondriaMitochondrial DynamicsMitochondrial Membrane Transport ProteinsNeoplasm MetastasisOxidative PhosphorylationReactive Oxygen SpeciesDeoxyglucoseGlucoseGTP PhosphohydrolasesMfn1 protein, humanMitochondrial Membrane Transport ProteinsReactive Oxygen Species

Identifiers

PMID31819189
PMCPMC7052272
OpenAlexW2992585254

What OpenQuestion holds

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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.