Evidence map›Paper›PMID 34273954›Full record

ArticleBMC cancer2021

MARCH6 promotes hepatocellular carcinoma development through up-regulation of ATF2.

Jie Sun, Zheng Dong, Zhengyao Chang, Hongfei Liu, Qiyu Jiang, Deyuan Zhang, Shanshan Lu, Xiaodong Jia, Dawei Wu, Aaron Ge and 3 more

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

12 citing papers in PubMed, 14 citations in OpenAlex.

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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

13 authors at 3 institutions in 2 countries.

Jie Sun *Comprehensive Liver Cancer Center, The Fifth Medical Center of PLA General Hospital, Beijing, 100039, China.
Zheng Dong *Comprehensive Liver Cancer Center, The Fifth Medical Center of PLA General Hospital, Beijing, 100039, China.
Zhengyao Chang *Department of General Surgery, The Fifth Medical Center of PLA General Hospital, Beijing, 100039, China.
Hongfei LiuBeijing Syngentech Co., Ltd., Beijing, 102206, China.
Qiyu JiangResearch Center for Clinical and Translational Medicine, The Fifth Medical Center of PLA General Hospital, Beijing, 100039, China.
Deyuan ZhangComprehensive Liver Cancer Center, The Fifth Medical Center of PLA General Hospital, Beijing, 100039, China.
Shanshan LuComprehensive Liver Cancer Center, The Fifth Medical Center of PLA General Hospital, Beijing, 100039, China.
Xiaodong JiaComprehensive Liver Cancer Center, The Fifth Medical Center of PLA General Hospital, Beijing, 100039, China.
Dawei WuComprehensive Liver Cancer Center, The Fifth Medical Center of PLA General Hospital, Beijing, 100039, China.
Aaron GeComprehensive Liver Cancer Center, The Fifth Medical Center of PLA General Hospital, Beijing, 100039, China.
Pan ZhaoDepartment of Infectious Diseases, The Fifth Medical Center of PLA General Hospital, Beijing, 100039, China. doczhaopan@126.com.
Jing WangState key Laboratory of Toxicology and Medical Countermeasures, Beijing Institute of Pharmacology and Toxicology, Beijing, 100850, China. JingWang@bmi.ac.cn.ORCID http://orcid.org/0000-0003-3278-6346
Yinying LuComprehensive Liver Cancer Center, The Fifth Medical Center of PLA General Hospital, Beijing, 100039, China. Luyinying1973@163.com.
Chinese PLA General Hospital · CNInstitute of Pharmacology · CZSyngenta (China) · CN

Funding

Ministry of Science and Technology of China 2018ZX09J18107National Natural Science Foundation of China 81672467, 81672368, 81501652Natural Science Foundation of Beijing 7172207, 5162026, 7202193
6 · The paper itself

Abstract

backgroundHepatocellular carcinoma (HCC) is a common cause of cancer mortality worldwide. Recent studies have shown that the polytopic enzyme membrane associated ring-CH-type finger 6 (MARCH6) participates in tumorigenesis, but its function in HCC development needs to be investigated. This study aimed to explore the role of MARCH6 in HCC.

methodsExpression of MARCH6 in human HCC samples was checked by immunohistochemical staining assay. Clinical relevance of MARCH6 and activating transcription factor 2 (ATF2) was analyzed from TCGA database. CCK-8, EdU staining, colony formation and transwell were performed to assess cell proliferation, growth and migration. Xenografted tumorigenesis was used to examine in vivo role MARCH6. Immunoblotting was applied to detect protein abundance.

resultsWe found that MARCH6 expression was elevated in human HCC samples. Over-expression of MARCH6 was associated with poor prognosis of HCC patients. Up-expression of MARCH6 promoted cell growth and migration of HCC cells. In contrast, the HCC cell growth and migration were suppressed by MARCH6 knockdown. Furthermore, the DNA synthesis was enhanced by MARCH6. The expression of ATF2 was potentiated by MARCH6 over-expression, while it was suppressed by MARCH6 silencing. TCGA database showed positive correlation between the expression of MARCH6 and ATF2. Importantly, ATF2 expression contributed to the oncogenic function of HCC cells.

conclusionOur findings suggest that MARCH6-mediated ATF2 up-regulation contributes to HCC development. MARCH6 may be a promising target for the diagnosis and treatment of HCC.

Indexed as

Activating Transcription Factor 2AnimalsCarcinoma, HepatocellularCell MovementCell ProliferationFemaleHumansLiver NeoplasmsMembrane ProteinsMiceMice, NudeUbiquitin-Protein LigasesUp-RegulationActivating Transcription Factor 2ATF2 protein, humanMARCHF6 protein, humanMembrane ProteinsUbiquitin-Protein LigasesATF2Hepatocellular carcinomaMARCH6MigrationProliferation

Identifiers

PMID34273954
PMCPMC8285810
OpenAlexW3197201158

What OpenQuestion holds

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LicenceCC BY
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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.