Evidence map›Paper›PMID 31911859›Full record

ArticleAmerican journal of cancer research2019

USP37 is a SNAI1 deubiquitinase.

Zhenna Xiao, Liang Chang, Jongchan Kim, Peijing Zhang, Qinglei Hang, Shannon Yap, Youming Guo, Zhicheng Zhou, Liyong Zeng, Xiaoyu Hu and 3 more

Open access · greenAbstract read
In one paragraph

Article in American journal of cancer research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.5field-weighted citation impact, top 34% 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

12 citing papers in PubMed, 16 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

13 authors at 1 institution in 3 countries.

Zhenna XiaoDepartment of Experimental Radiation Oncology, The University of Texas MD Anderson Cancer Center Houston 77030, Texas, USA.
Liang ChangDepartment of Experimental Radiation Oncology, The University of Texas MD Anderson Cancer Center Houston 77030, Texas, USA.
Jongchan KimDepartment of Experimental Radiation Oncology, The University of Texas MD Anderson Cancer Center Houston 77030, Texas, USA.
Peijing ZhangDepartment of Experimental Radiation Oncology, The University of Texas MD Anderson Cancer Center Houston 77030, Texas, USA.
Qinglei HangDepartment of Experimental Radiation Oncology, The University of Texas MD Anderson Cancer Center Houston 77030, Texas, USA.
Shannon YapDepartment of Experimental Radiation Oncology, The University of Texas MD Anderson Cancer Center Houston 77030, Texas, USA.
Youming GuoDepartment of Experimental Radiation Oncology, The University of Texas MD Anderson Cancer Center Houston 77030, Texas, USA.
Zhicheng ZhouDepartment of Experimental Radiation Oncology, The University of Texas MD Anderson Cancer Center Houston 77030, Texas, USA.
Liyong ZengDepartment of Experimental Radiation Oncology, The University of Texas MD Anderson Cancer Center Houston 77030, Texas, USA.
Xiaoyu HuDepartment of Experimental Radiation Oncology, The University of Texas MD Anderson Cancer Center Houston 77030, Texas, USA.
Ashley SiverlyDepartment of Experimental Radiation Oncology, The University of Texas MD Anderson Cancer Center Houston 77030, Texas, USA.
Yutong SunDepartment of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center Houston 77030, Texas, USA.
Li MaDepartment of Experimental Radiation Oncology, The University of Texas MD Anderson Cancer Center Houston 77030, Texas, USA.
The University of Texas MD Anderson Cancer Center · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
Regulation of metastasis and epithelial-mesenchymal transition by microRNAsR01CA166051 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI MA, LI · 2012 to 2023
$3.4M
Epithelial-mesenchymal transition regulators in radioresistance and DNA repairR01CA181029 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI MA, LI · 2014 to 2018
$1.7M
NCI NIH HHS P30 CA016672NCI NIH HHS R01 CA166051NCI NIH HHS R01 CA181029
6 · The paper itself

Abstract

SNAI1, an epithelial-mesenchymal transition (EMT)-inducing transcription factor, promotes tumor metastasis and resistance to apoptosis and chemotherapy. SNAI1 protein levels are tightly regulated by proteolytic ubiquitination. Here, we identified USP37 as a SNAI1 deubiquitinase that removes the polyubiquitination chain from SNAI1 and prevents its proteasomal degradation. USP37 directly binds, deubiquitinates, and stabilizes SNAI1. Overexpression of wild-type USP37, but not its catalytically inactive mutant C350S, promotes cancer cell migration. Importantly, depletion of USP37 downregulates endogenous SNAI1 protein and suppresses cell migration, which can be reversed by re-expression of SNAI1. Taken together, our findings suggest that USP37 is a SNAI1 deubiquitinase and a potential therapeutic target to inhibit tumor metastasis.

Indexed as

degradationdeubiquitinaseEMTSNAI1USP37

Identifiers

PMID31911859
PMCPMC6943346
OpenAlexW3008024970

What OpenQuestion holds

Textmetadata
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.