Evidence map›Paper›PMID 33078596›Full record

ArticleJournal of gynecologic oncology2020

High mobility group box 3 promotes cervical cancer proliferation by regulating Wnt/β-catenin pathway.

Shichao Zhuang, Xiaohui Yu, Ming Lu, Yujiao Li, Ning Ding, Yumei Ding

Open access · diamondAbstract read
In one paragraph

Article in Journal of gynecologic oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

13 citing papers in PubMed, 19 citations in OpenAlex.

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  6. Structure and Functions of HMGB3 Protein.International journal of molecular sciences · 2024
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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 1 institution in 1 country.

Shichao ZhuangDepartment of Gynaecology, ZIBO Central Hospital, Zibo, Shandong, China.ORCID https://orcid.org/0000-0001-9383-6787
Xiaohui YuDepartment of Gynaecology, ZIBO Central Hospital, Zibo, Shandong, China.ORCID https://orcid.org/0000-0002-7381-9709
Ming LuDepartment of Gynaecology, ZIBO Central Hospital, Zibo, Shandong, China.ORCID https://orcid.org/0000-0003-3258-3274
Yujiao LiDepartment of Gynaecology, ZIBO Central Hospital, Zibo, Shandong, China.ORCID https://orcid.org/0000-0003-3851-830X
Ning DingDepartment of Gynaecology, ZIBO Central Hospital, Zibo, Shandong, China.ORCID https://orcid.org/0000-0002-2729-6126
Yumei DingDepartment of Gynaecology, ZIBO Central Hospital, Zibo, Shandong, China. meihua1072@126.com.ORCID https://orcid.org/0000-0002-2666-7386
Central Hospital of Zibo · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveHigh mobility group box 3 (HMGB3) plays an important role in the development of various cancer. This study aims to explore whether HMGB3 regulates cervical cancer (CC) progression and elucidate the underlying mechanism.

methodsHMGB3 expression in clinical patients' tumor samples were determined by real-time quantitative polymerase chain reaction (qRT-PCR) and western blot. HMGB3 overexpression/knockdown were used to investigate its function. Cell apoptosis and cycle were detected by Annexin V/PI staining and flow cytometry. In vivo tumor model was made by subcutaneous injection of HeLa cells transfected with shRNAs targeting HMGB3 (sh-HMGB31) into the flank area of nude mice. Western blot was used to detect the levels of β-catenin, c-Myc, and matrix metalloproteinase-7 (MMP-7) in Hela and CaSki cells transfected with sh-HMGB3 or shRNAs targeting β-catenin.

resultsBoth messenger RNA and protein levels of HMGB3 were upregulated in CC tissues from patients. High expression level of HMGB3 had positive correlation with serosal invasion, lymph metastasis, and tumor sizes in CC patient. Functional experiments showed that HMGB3 could promote CC cell proliferation both in vitro and in vivo. The expression levels of c-Myc and MMP-7 were increased, resulting in regulating cell apoptosis, cell cycle, and activating Wnt/β-catenin pathway.

conclusionsOur data indicated that HMGB3 may serve as an oncoprotein. It could be used as a potential prognostic marker and represent a promising therapeutic strategy for CC treatment.

Indexed as

beta CateninUterine Cervical NeoplasmsAdultAnimalsApoptosisCell Line, TumorCell ProliferationFemaleGene Expression Regulation, NeoplasticHeLa CellsHMGB3 ProteinHumansMiceMice, NudeMiddle AgedWnt Signaling Pathwaybeta CateninHMGB3 Proteinbeta CateninCell ProliferationCervical CancerHMGB3 ProteinshRNA

Identifiers

PMID33078596
PMCPMC7593223
OpenAlexW3089166650

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.