Evidence map›Paper›PMID 35880246›Full record

ArticleCancer science2022

Ubiquitin-specific protease 28 deubiquitinates TCF7L2 to govern the action of the Wnt signaling pathway in hepatic carcinoma.

Xiao Sun, Mengjiao Cai, Lingzhi Wu, Xinghua Zhen, Yuetong Chen, Jin Peng, Suxia Han, Pumin Zhang

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

17 citing papers in PubMed, 21 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

8 authors at 3 institutions in 1 country.

Xiao SunDepartment of Oncology, The First Affiliated Hospital, Xi'an Jiaotong University Medical College, Xi'an, China.
Mengjiao CaiDepartment of Oncology, The First Affiliated Hospital, Xi'an Jiaotong University Medical College, Xi'an, China.
Lingzhi WuZhejiang Provincial Key Laboratory of Pancreatic Disease, The First Affiliated Hospital of Zhejiang University, Hangzhou, China.
Xinghua ZhenZhejiang Provincial Key Laboratory of Pancreatic Disease, The First Affiliated Hospital of Zhejiang University, Hangzhou, China.
Yuetong ChenDepartment of Oncology, The First Affiliated Hospital, Xi'an Jiaotong University Medical College, Xi'an, China.
Jin PengZhejiang Provincial Key Laboratory of Pancreatic Disease, The First Affiliated Hospital of Zhejiang University, Hangzhou, China.
Suxia HanDepartment of Oncology, The First Affiliated Hospital, Xi'an Jiaotong University Medical College, Xi'an, China.ORCID https://orcid.org/0000-0003-0842-3908
Pumin ZhangZhejiang Provincial Key Laboratory of Pancreatic Disease, The First Affiliated Hospital of Zhejiang University, Hangzhou, China.ORCID https://orcid.org/0000-0003-4063-3008
First Affiliated Hospital of Xi'an Jiaotong University · CNFirst Affiliated Hospital Zhejiang University · CNZhejiang Chinese Medical University · CN

Funding

Innovation Capacity Support Plan of Shaanxi Province 2018TD-002National Key R&D Program of China 2018YFA0507500National Natural Science Foundation of China 81773032
6 · The paper itself

Abstract

Overexpression of ubiquitin-specific protease 28 (USP28) is found in hepatic carcinoma. It is unclear whether the deubiquitinase plays a role in hepatocarcinogenesis. Deregulation of the Wnt signaling pathway is frequently associated with liver cancer. Transcription factor 7-like 2 (TCF7L2) is an important downstream transcription factor of the Wnt/β-catenin signaling pathway, but the mechanisms by which TCF7L2 itself is regulated have not yet been revealed. Here, we report that USP28 promotes the activity of the Wnt signaling pathway through maintaining the stability of TCF7L2. We further show that FBXW7 is the E3 ubiquitin ligase for TCF7L2. By regulating the levels of TCF7L2, USP28 modulates the Wnt/β-catenin signaling in liver cancer and USP28 depletion or inhibition by a small molecule inhibitor leads to a halt of growth in liver cancer cells. These results suggest that USP28 could be a potential therapeutic target for liver cancer.

Indexed as

Carcinoma, HepatocellularLiver Neoplasmsbeta CateninCell Line, TumorDeubiquitinating EnzymesF-Box-WD Repeat-Containing Protein 7HumansT Cell Transcription Factor 1Transcription Factor 7-Like 2 ProteinUbiquitin-Protein LigasesUbiquitin-Specific ProteasesUbiquitin ThiolesteraseWnt Signaling Pathwaybeta CateninDeubiquitinating EnzymesF-Box-WD Repeat-Containing Protein 7T Cell Transcription Factor 1TCF7L2 protein, humanTranscription Factor 7-Like 2 ProteinUbiquitin-Protein LigasesUbiquitin-Specific ProteasesUbiquitin ThiolesteraseUSP28 protein, humandeubiquitinationliver cancerTCF7L2USP28Wnt signaling

Identifiers

PMID35880246
PMCPMC9530868
OpenAlexW4287877810

What OpenQuestion holds

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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.