Evidence map›Paper›PMID 34036684›Full record

ArticleCancer science2021

Fucosyltransferase 8 regulation and breast cancer suppression by transcription factor activator protein 2γ.

Minxing Ma, Dong Guo, Zengqi Tan, Jun Du, Feng Guan, Xiang Li

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

21 citing papers in PubMed, 34 citations in OpenAlex.

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  11. Core fucosylation and its roles in gastrointestinal glycoimmunology.World journal of gastrointestinal oncology · 2023
    Review
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  15. Effect and Mechanism Analysis of PigInternational journal of molecular sciences · 2022
    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

6 authors at 4 institutions in 1 country.

Minxing MaDepartment of Oncology, The Fifth People's Hospital of Qinghai Province, Xining, China.ORCID https://orcid.org/0000-0003-1765-3932
Dong GuoDepartment of Central Lab, Cheeloo College of Medicine, Weihai Municipal Hospital, Shandong University, Weihai, China.
Zengqi TanKey Laboratory of Resource Biology and Biotechnology in Western China, Ministry of Education, Joint International Research Laboratory of Glycobiology and Medicinal Chemistry, College of Life Sciences, Northwest University, Xi'an, China.
Jun DuDepartment of Oncology, The Fifth People's Hospital of Qinghai Province, Xining, China.
Feng GuanKey Laboratory of Resource Biology and Biotechnology in Western China, Ministry of Education, Joint International Research Laboratory of Glycobiology and Medicinal Chemistry, College of Life Sciences, Northwest University, Xi'an, China.
Xiang LiInstitute of Hematology, School of Medicine, Northwest University, Xi'an, China.
Ministry of Education of the People's Republic of China · CNQinghai No.3 People's Hospital · CNNorthwest University · CNShandong University · CN

Funding

National Natural Science Foundation of China 31971211National Natural Science Foundation of China 81802654National Science and Technology Major Project of China 2018ZX10302205Natural Science Foundation of Shaanxi Province 2019JZ-22Youth Science Foundation of the Fifth People's Hospital of Qinghai province 2017-Y-01
6 · The paper itself

Abstract

Alterations of glycosyltransferase expression are often associated with tumor occurrence and progression. Among the many glycosyltransferases, increased expression of fucosyltransferase 8 (FUT8) has been frequently observed to be involved in progression and metastasis of various types of cancer. The regulatory mechanisms of FUT8 expression remain unclear. FUT8 expression was shown, in this study, to be elevated in breast cancer. Systematic analysis revealed that transcription factor activator protein 2γ (AP-2γ) is the target gene of microRNA-10b (miR-10b), which we previously identified as a positive regulator of FUT8. Overexpression of AP-2γ inhibited FUT8 expression, with associated reduction of cell invasiveness and migration ability. AP-2γ was capable of binding to transcription factor STAT3, and phosphorylation of STAT3 induced transcription of the FUT8 gene. On the basis of our findings, we propose that binding of AP-2γ to STAT3 results in formation of the AP-2γ/STAT3 complex and consequent inhibition of STAT3 phosphorylation, thereby preventing entry of p-STAT3 into the nucleus to initiate FUT8 transcription. This study clarifies the molecular mechanisms whereby transcription factor AP-2γ regulates FUT8 expression in breast cancer.

Indexed as

AnimalsBreast NeoplasmsCell Line, TumorCell MovementCell NucleusFemaleFucosyltransferasesGene Expression Regulation, NeoplasticHumansMCF-7 CellsMembrane GlycoproteinsMiceNeoplasm InvasivenessNeoplasm TransplantationPhosphorylationReceptors, ImmunologicFucosyltransferasesGlycoprotein 6-alpha-L-fucosyltransferaseLILRB2 protein, humanMembrane GlycoproteinsReceptors, ImmunologicSTAT3 protein, humanSTAT3 Transcription FactorTFAP2C protein, humanTranscription Factor AP-2AP-2γbreast cancerfucosyltransferase 8miR-10bSTAT3

Identifiers

PMID34036684
PMCPMC8353918
OpenAlexW3163977479

What OpenQuestion holds

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LicenceCC BY-NC
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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.