Evidence map›Paper›PMID 39763353›Full record

ArticleThe Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology2024

WISP1 Inhibits Hepatocellular Carcinoma Cell Proliferation by Promoting CyclinD1 Ubiquitination and Downregulating its Expression.

Jinlong Yan, Jun Wen Hu, Na Cheng, Nuoya Li, Anqi Xin, Zhipeng Wu, Zhengyi Wu, Jun Lei, Shouhua Zhang, Jinping Yao

Abstract read
In one paragraph

Article in The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Article
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.

Jinlong YanDepartment of General Surgery, The Second AffiliatedHospital, Jiangxi Medical College, Nanchang University, Jiangxi, ChinaORCID 0000-0002-7040-0275
Jun Wen HuDepartment of General Surgery, The Second AffiliatedHospital, Jiangxi Medical College, Nanchang University, Jiangxi, China
Na ChengDepartment of Hospital Infection Control, The First Affiliated Hospital of Nanchang University, Jiangxi, China
Nuoya LiDepartment of Hepatobiliary Surgery, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou ChinaORCID 0000-0001-7323-0825
Anqi XinDepartment of Operation Room, The Second Affiliated Hospital, Nanchang University Jiangxi Medical College, Jiangxi, ChinaORCID 0000-0002-2009-4492
Zhipeng WuDepartment of General Surgery, The Second AffiliatedHospital, Jiangxi Medical College, Nanchang University, Jiangxi, ChinaORCID 0000-0002-6011-1840
Zhengyi WuDepartment of General Surgery, The Second AffiliatedHospital, Jiangxi Medical College, Nanchang University, Jiangxi, ChinaORCID 0000-0002-8371-6885
Jun LeiDepartment of General Surgery, The Second AffiliatedHospital, Jiangxi Medical College, Nanchang University, Jiangxi, China
Shouhua ZhangDepartment of General Surgery, The Second AffiliatedHospital, Jiangxi Medical College, Nanchang University, Jiangxi, ChinaORCID 0000-0002-8225-1350
Jinping YaoDepartment of Endocrinology, the Fourth Affiliated Hospital of Nanchang University Jiangxi Medical College, Jiangxi, ChinaORCID 0009-0007-8205-0237

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background/Aims: Hepatocellular carcinoma (HCC), a leading cause of cancer-related deaths, is often linked to dysregulated cell cycle proteins. This study focuses on the role of WISP1 in modulating Cyclin D1, a key cell cycle regulator, in HCC. Materials and Methods: The study used HCCLM3 and Hep3B cells to assess the expression of Cyclin D1 and cell proliferation following the treatment of WISP1. This was achieved through Western blot, qRT-PCR, and EdU assays. Additionally, animal studies were conducted to evaluate the effects of WISP1 treatment on Cyclin D1 expression and cell proliferation. Results: Overexpression of WISP1 in HCC cells led to a marked decrease in Cyclin D1 protein levels and reduced cell proliferation. WISP1 influences Cyclin D1 through post-translational modifications, particularly ubiquitination and proteasomal degradation. Conclusion: The findings revealed that WISP1’s modulation of Cyclin D1 plays a critical role in inhibiting HCC cell growth, highlighting a potential therapeutic target for HCC treatment.

Indexed as

Carcinoma, HepatocellularCCN Intercellular Signaling ProteinsCell ProliferationCyclin D1Liver NeoplasmsProto-Oncogene ProteinsAnimalsCell Line, TumorDown-RegulationGene Expression Regulation, NeoplasticHumansMiceUbiquitinationCCN4 protein, humanCCND1 protein, humanCCN Intercellular Signaling ProteinsCyclin D1Proto-Oncogene ProteinsCyclinD1hepatocellular carcinomaUbiquitinationWISP1

Identifiers

PMID39763353
PMCPMC12001460

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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.