Evidence map›Paper›PMID 32273758›Full record

ArticleCancer management and research2020

Down-regulation of USP8 Inhibits Cholangiocarcinoma Cell Proliferation and Invasion.

Xu Jing, Yingjie Chen, Ye Chen, Guangyan Shi, Shuanghao Lv, Nana Cheng, Chaolin Feng, Zhen Xin, Liping Zhang, Jing Wu

Open access · goldAbstract read
In one paragraph

Article in Cancer management and research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.5field-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

18 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
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  7. Deubiquitylating Enzymes in Cancer and Immunity.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2023
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  15. Deubiquitinases: Modulators of Different Types of Regulated Cell Death.International journal of molecular sciences · 2021
    Review
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  17. Article
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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

10 authors at 3 institutions in 1 country.

Xu JingDepartment of Clinical Laboratory, The Second Hospital of Shandong University, Jinan, People's Republic of China.
Yingjie ChenDepartment of Clinical Laboratory, The Second Hospital of Shandong University, Jinan, People's Republic of China.
Ye ChenDepartment of Physiology and Pathophysiology, School of Basic Medicine, Shandong University, Jinan, People's Republic of China.
Guangyan ShiDepartment of Clinical Laboratory, The Second Hospital of Shandong University, Jinan, People's Republic of China.
Shuanghao LvDepartment of Clinical Laboratory, The Second Hospital of Shandong University, Jinan, People's Republic of China.
Nana ChengDepartment of Clinical Laboratory, The Second Hospital of Shandong University, Jinan, People's Republic of China.
Chaolin FengDepartment of Clinical Laboratory, The Second Hospital of Shandong University, Jinan, People's Republic of China.
Zhen XinDepartment of Clinical Laboratory, The Second Hospital of Shandong University, Jinan, People's Republic of China.
Liping ZhangThe First Affiliated Hospital of Henan University of Chinese Medicine, Zhengzhou, People's Republic of China.
Jing WuDepartment of Pharmacy, The Second Hospital of Shandong University, Jinan, People's Republic of China.
Second Hospital of Shandong University · CNShandong University · CNFirst Affiliated Hospital of Henan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveCholangiocarcinoma is the second most common primary hepatobiliary malignancy with high incidence and recurrence rate. Ubiquitin-specific protease 8 (USP8) is recently reported to be involved in tumor progression. Herein, we aimed to investigate the effects of USP8 on the growth and metastasis abilities of cholangiocarcinoma cells.

methodsThe siRNA interference was used to knock down USP8 in cholangiocarcinoma cell lines QBC939 and RBE; Hucct-1 cells were transfected with pcDNA3.1-USP8 to up-regulate its expression. The effects of USP8 on cholangiocarcinoma were detected by cell function assays. We analyzed the expressions of USP8, Bcl2, Bax, cleaved caspase-3, cleaved caspase-9, Akt, p-Akt, Cyclin D1 and P70S6K by Western blot analysis.

resultsWe demonstrated that knockdown of USP8 significantly inhibited the proliferation, migration and invasion of QBC939 and RBE cells in vitro, while USP8 overexpression showed significant promoting effects on Hucct-1 cells. Moreover, silencing of USP8 also promoted apoptosis in cholangiocarcinoma cells by regulating the Bcl-2/Bax axis and Caspase cascade; up-regulation of USP8 decreased apoptosis in Hucct-1 cells. Importantly, knockdown of USP8 inhibited activation of the Akt signaling pathway by decreasing the phosphorylation level of Akt and up-regulated p53 expression, while USP8 overexpression increased activation of the Akt signaling pathway in Hucct-1 cells. Further, IGF-1 could reverse the inhibitory effects of USP8 knockdown on the Akt signaling pathway and the proliferation of QBC939 and RBE cells.

conclusionTaken together, our findings suggest that USP8 exerts an oncogenic role in the progression of cholangiocarcinoma and may be a potential therapeutic target for cholangiocarcinoma treatment.

Indexed as

Akt signaling pathwaycholangiocarcinomaubiquitin-specific protease 8

Identifiers

PMID32273758
PMCPMC7113805
OpenAlexW3012695620

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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.