Evidence map›Paper›PMID 33255748›Full record

ArticleInternational journal of molecular sciences2020

Knocking down USP39 Inhibits the Growth and Metastasis of Non-Small-Cell Lung Cancer Cells through Activating the p53 Pathway.

Jiahui Yuan, Gongye Zhang, Xiaomei Li, Qiujuan Ma, Weipeng Cheng, Weiwei Wang, Bing Zhang, Tianhui Hu, Gang Song

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 18% 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

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 31 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

9 authors at 1 institution in 1 country.

Jiahui YuanCancer Research Center, School of Medicine, Xiamen University, Xiamen 361102, China.ORCID 0000-0002-3183-5719
Gongye ZhangCancer Research Center, School of Medicine, Xiamen University, Xiamen 361102, China.
Xiaomei LiCancer Research Center, School of Medicine, Xiamen University, Xiamen 361102, China.
Qiujuan MaCancer Research Center, School of Medicine, Xiamen University, Xiamen 361102, China.
Weipeng ChengCancer Research Center, School of Medicine, Xiamen University, Xiamen 361102, China.
Weiwei WangCancer Research Center, School of Medicine, Xiamen University, Xiamen 361102, China.
Bing ZhangDepartment of Basic Medicine, School of Medicine, Xiamen University, Xiamen 361102, China.
Tianhui HuCancer Research Center, School of Medicine, Xiamen University, Xiamen 361102, China.
Gang SongCancer Research Center, School of Medicine, Xiamen University, Xiamen 361102, China.ORCID 0000-0003-2507-5853
Xiamen University · CN

Funding

the national natural science foundation of China 81872045the special fund for public welfare research institutes of Fujian Province 2020R11010032-3
6 · The paper itself

Abstract

Ubiquitin-specific protease 39 (USP39), a member of the deubiquitinating enzyme family, has been reported to participate in cytokinesis and metastasis. Previous studies determined that USP39 functions as an oncogenic factor in various types of cancer. Here, we reported that USP39 is frequently overexpressed in human lung cancer tissues and non-small-cell lung cancer (NSCLC) cell lines. USP39 knockdown inhibited the proliferation and colony formation of A549 and HCC827 cells and decreased tumorigenic potential in nude mice. Specifically, knocking down USP39 resulted in cell cycle arrest at G2/M and subsequent apoptosis through the activation of the p53 pathway, including upregulation of p21, cleaved-cas3, cleaved-cas9 and downregulation of CDC2 and CycinB1. Moreover, USP39 knockdown significantly inhibited migration and invasion of A549 and HCC827 cells, also via activation of the p53 pathway, and downregulation of MMP2 and MMP9. Importantly, we verified these results in metastasis models in vivo. Collectively, these results not only establish that USP39 functions as an oncogene in lung cancer, but reveal that USP39 has an essential role in regulating cell proliferation and metastasis via activation of the p53 pathway.

Indexed as

A549 CellsAnimalsApoptosisCarcinoma, Non-Small-Cell LungCell Cycle CheckpointsCell ProliferationGene Expression Regulation, NeoplasticGene Knockdown TechniquesHeterograftsHumansMatrix Metalloproteinase 2Matrix Metalloproteinase 9MiceNeoplasm MetastasisSignal TransductionTranscriptional ActivationMatrix Metalloproteinase 2Matrix Metalloproteinase 9MMP2 protein, humanMMP9 protein, humanTP53 protein, humanTumor Suppressor Protein p53Ubiquitin-Specific ProteasesUSP39 protein, humangrowthmetastasisp53 pathwayproliferationUSP39

Identifiers

PMID33255748
PMCPMC7728369
OpenAlexW3107889627

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.