Evidence map›Paper›PMID 27030811›Full record

ArticleCell discovery

Ubiquitin-specific protease 22 is a deubiquitinase of CCNB1.

Zhenghong Lin, Can Tan, Quan Qiu, Sinyi Kong, Heeyoung Yang, Fang Zhao, Zhaojian Liu, Jinping Li, Qingfei Kong, Beixue Gao and 4 more

Open access · goldAbstract read
In one paragraph

Article in Cell discovery. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

62 citing papers in PubMed, 83 citations in OpenAlex.

  1. Article
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  8. Bioinformatic analysis of the role of USP22 expression in hepatocellular carcinoma.International journal of clinical and experimental pathology · 2025
    Article
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2 more citing papers are in PubMed but not listed here.

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

14 authors at 3 institutions in 2 countries.

Zhenghong LinDepartment of Pathology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Can TanDepartment of Pathology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Quan QiuDepartment of Pathology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Sinyi KongDepartment of Pathology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Heeyoung YangDepartment of Pathology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Fang ZhaoDepartment of Pathology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Zhaojian LiuDepartment of Pathology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Jinping LiDepartment of Pathology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Qingfei KongDepartment of Pathology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Beixue GaoDepartment of Pathology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Terry BarrettDepartment of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Guang-Yu YangDepartment of Pathology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Jianing ZhangSchool of Life Science and Medicine, Dalian University of Technology, Panjin, China.
Deyu FangDepartment of Pathology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA; School of Life Science and Medicine, Dalian University of Technology, Panjin, China.
Northwestern University · USDalian University · CNDalian University of Technology · CN

Funding

The roles of Sirt1, a deacetylase, in immune tolerance and autoimmunityR01AI079056 · NIAID · UNIVERSITY OF MISSOURI-COLUMBIA · PI FANG, DEYU · 2008 to 2017
$3.3M
A novel target for type 1 diabetesDP2DK083050 · NIDDK · UNIVERSITY OF MISSOURI-COLUMBIA · PI FANG, DEYU · 2008 to 2010
$2.4M
Simultaneous Targeting of IRE1a in B Cells and Macrophages for Lupus TherapyR01AR066634 · NIAMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI FANG, DEYU, ZHANG, KEZHONG · 2014 to 2018
$1.7M
The roles of Synoviolin in immune tolerance and autoimmunityR01AI108634 · NIAID · NORTHWESTERN UNIVERSITY AT CHICAGO · PI FANG, DEYU · 2014 to 2017
$1.5M
The roles of Sirt1, a deacetylase, in immune tolerance and autoimmunityR56AI079056 · NIAID · NORTHWESTERN UNIVERSITY AT CHICAGO · PI FANG, DEYU · 2012 to 2012
$386k
NIAID NIH HHS R01 AI079056NIAID NIH HHS R01 AI108634NIAID NIH HHS R56 AI079056NIAMS NIH HHS R01 AR066634NIDDK NIH HHS DP2 DK083050
6 · The paper itself

Abstract

The elevated level of CCNB1 indicates more aggressive cancer and poor prognosis. However, the factors that cause CCNB1 upregulation remain enigmatic. Herein, we identify USP22 as a CCNB1 interactor and discover that both USP22 and CCNB1 are dramatically elevated with a strong positive correlation in colon cancer tissues. USP22 stabilizes CCNB1 by antagonizing proteasome-mediated degradation in a cell cycle-specific manner. Phosphorylation of USP22 by CDK1 enhances its activity in deubiquitinating CCNB1. The ubiquitin ligase anaphase-promoting complex (APC/C) targets USP22 for degradation by using the substrate adapter CDC20 during cell exit from M phase, presumably allowing CCNB1 degradation. Finally, we discover that USP22 knockdown leads to slower cell growth and reduced tumor size. Our study demonstrates that USP22 is a CCNB1 deubiquitinase, suggesting that targeting USP22 might be an effective approach to treat cancers with elevated CCNB1 expression.

Indexed as

APC8CCNB1cell cycletumorigenesisUSP22

Identifiers

PMID27030811
PMCPMC4809424
OpenAlexW2413323956

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.