Evidence map›Paper›PMID 35313071›Full record

ArticleMolecular oncology2022

DRP1 contributes to head and neck cancer progression and induces glycolysis through modulated FOXM1/MMP12 axis.

Tai-Lin Huang, Chuang-Rung Chang, Chih-Yen Chien, Gong-Kai Huang, Yi-Fan Chen, Li-Jen Su, Hsin-Ting Tsai, Yu-Sheng Lin, Fu-Min Fang, Chang-Han Chen

Open access · goldAbstract read
In one paragraph

Article in Molecular oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

26 citing papers in PubMed, 36 citations in OpenAlex.

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  9. The Role of N6-Methyladenosine in Mitochondrial Dysfunction and Pathology.International journal of molecular sciences · 2025
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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 at 6 institutions in 2 countries.

Tai-Lin HuangDivision of Hematology-Oncology, Department of Internal Medicine, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Taiwan.
Chuang-Rung ChangInstitute of Biotechnology and Department of Medical Science, National Tsing Hua University, Hsinchu, Taiwan.ORCID 0000-0002-6124-5429
Chih-Yen ChienKaohsiung Chang Gung Head and Neck Oncology Group, Cancer Center, Kaohsiung Chang Gung Memorial Hospital, Taiwan.
Gong-Kai HuangDepartment of Anatomic Pathology, Chang Gung Memorial Hospital, Kaohsiung, Taiwan.
Yi-Fan ChenDepartment of Orthopedic Surgery, Chang Gung Memorial Hospital, Kaohsiung, Taiwan.
Li-Jen SuDepartment of Biomedical Sciences and Engineering, Education and Research Center for Technology Assisted Substance Abuse Prevention and Management, and Core Facilities for High Throughput Experimental Analysis, National Central University, Taoyuan County, Taiwan.
Hsin-Ting TsaiInstitute of Medicine, Chung Shan Medical University, Taichung, Taiwan.
Yu-Sheng LinState Key Laboratory of Optoelectronic Materials and Technologies, School of Electronics and Information Technology, Sun Yat-Sen University, Guangzhou, China.
Fu-Min FangKaohsiung Chang Gung Head and Neck Oncology Group, Cancer Center, Kaohsiung Chang Gung Memorial Hospital, Taiwan.
Chang-Han ChenInstitute of Medicine, Chung Shan Medical University, Taichung, Taiwan.ORCID 0000-0003-1892-6680
Chang Gung University · TWChung Shan Medical University Hospital · TWKaohsiung Chang Gung Memorial Hospital · TWNational Central University · TWNational Tsing Hua University · TWSun Yat-sen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Abnormal DRP1 expression has been identified in a variety of human cancers. However, the prognostic potential and mechanistic role of DRP1 in head and neck cancer (HNC) are currently poorly understood. Here, we demonstrated a significant upregulation of DRP1 in HNC tissues, and that DRP1 expression correlates with poor survival of HNC patients. Diminished DRP1 expression suppressed tumor growth and metastasis in both in vitro and in vivo models. DRP1 expression was positively correlated with FOXM1 and MMP12 expression in HNC patient samples, suggesting pathological relevance in the context of HNC development. Moreover, DRP1 depletion affected aerobic glycolysis through the downregulation of glycolytic genes, and overexpression of MMP12 in DRP1-depleted cells could help restore glucose consumption and lactate production. Using ChIP-qPCR, we showed that DRP1 modulates FOXM1 expression, which can enhance MMP12 transcription by binding to its promoter. We also showed that miR-575 could target 3'UTR of DRP1 mRNA and suppress DRP1 expression. Collectively, our study provides mechanistic insights into the role of DRP1 in HNC and highlights the potential of targeting the miR-575/DRP1/FOXM1/MMP12 axis as a novel therapy for the prevention of HNC progression.

Indexed as

DynaminsForkhead Box Protein M1Head and Neck NeoplasmsMatrix Metalloproteinase 12Cell Line, TumorCell ProliferationGene Expression Regulation, NeoplasticGlycolysisHumansMicroRNAsDNM1L protein, humanDynaminsForkhead Box Protein M1FOXM1 protein, humanMatrix Metalloproteinase 12MicroRNAsMIRN575 microRNA, humanMMP12 protein, humanDRP1FOXM1glycolysishead and neck cancermiR-575MMP12

Identifiers

PMID35313071
PMCPMC9251862
OpenAlexW4220831256

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.