Evidence map›Paper›PMID 30793486›Full record

ArticleJournal of cellular and molecular medicine2019

MARCH1 encourages tumour progression of hepatocellular carcinoma via regulation of PI3K-AKT-β-catenin pathways.

Lulu Xie, Hanhan Dai, Minjing Li, Wei Yang, Guohua Yu, Xia Wang, Peiyuan Wang, Wei Liu, Xuemei Hu, Mingdong Zhao

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2019. 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
1.9field-weighted citation impact, top 14% 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, 33 citations in OpenAlex.

  1. Review
  2. Article
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  4. Curcumin Inhibits the Growth of Hepatocellular CarcinomaRecent patents on anti-cancer drug discovery · 2025
    Article
  5. Review
  6. E3 ubiquitin ligase MARCH1 reduces inflammation and pyroptosis in cerebral ischemia-reperfusion injury via PCSK9 downregulation.Mammalian genome : official journal of the International Mammalian Genome Society · 2024
    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 at 2 institutions in 1 country.

Lulu XieDepartment of Imaging, Binzhou Medical University, Yantai, China.
Hanhan DaiDepartment of Imaging, Binzhou Medical University, Yantai, China.
Minjing LiMedicine and Pharmacy Research Center, Binzhou Medical University, Yantai, China.
Wei YangDepartment of Imaging, Binzhou Medical University, Yantai, China.
Guohua YuDepartment of Pathology, Yu Huang Ding Hospital, Yantai, China.
Xia WangDepartment of Oral Pathology, Binzhou Medical University, Yantai, China.
Peiyuan WangDepartment of Imaging, Binzhou Medical University, Yantai, China.
Wei LiuDepartment of Imaging, Binzhou Medical University, Yantai, China.
Xuemei HuDepartment of Immunology, Binzhou Medical University, Yantai, China.
Mingdong ZhaoDepartment of Imaging, Binzhou Medical University, Yantai, China.ORCID 0000-0002-9984-0506
Binzhou Medical University · CNYuhuangding Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Membrane-associated RING-CH-1 (MARCH1) is a membrane-anchored E3 ubiquitin ligase that is involved in a variety of cellular processes. MARCH1 was aberrantly expressed as a tumour promoter in ovarian cancer, but the signalling about the molecular mechanism has not yet been fully illuminated. Here, we first determined that MARCH1 was obviously highly expressed in human hepatocellular carcinoma samples and cells. In addition, our findings demonstrated that the proliferation, migration and invasion of hepatocellular carcinoma were suppressed, but the apoptosis was increased, as a result of MARCH1 knockdown by either siRNA targeting MARCH1 or pirarubicin treatment. Conversely, the proliferation, migration and invasion of hepatocellular carcinoma were obviously accelerated, and the apoptosis was decreased, by transfecting the MARCH1 plasmid to make MARCH1 overexpressed. Moreover, in vivo, the results exhibited a significant inhibition of the growth of hepatocellular carcinoma in nude mice, which were given an intra-tumour injection of siRNA targeting MARCH1. Furthermore, our study concluded that MARCH1 functions as a tumour promoter, and its role was up-regulated the PI3K-AKT-β-catenin pathways both in vitro and in vivo. In summary, our work determined that MARCH1 has an important role in the development and progression of hepatocellular carcinoma and may be used as a novel potential molecular therapeutic target in the future treatment of hepatocellular carcinoma.

Indexed as

Disease ProgressionAnimalsApoptosisbeta CateninCarcinoma, HepatocellularCell Line, TumorCell MovementCell ProliferationDown-RegulationFemaleGene Expression Regulation, NeoplasticGene SilencingHumansLiver NeoplasmsMagnetic Resonance ImagingMice, Inbred BALB Cbeta CateninMARCHF1 protein, humanPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktUbiquitin-Protein Ligasesapoptosishepatocellular carcinomaInvasionMARCH1migrationnude mouse modelpathwayspirarubicinproliferation

Identifiers

PMID30793486
PMCPMC6484336
OpenAlexW2918113937

What Socratic 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 Socratic graph.