Evidence map›Paper›PMID 26835714›Full record

ArticleCancer biomarkers : section A of Disease markers2016

Knockdown of USP39 by lentivirus-mediated RNA interference suppresses the growth of oral squamous cell carcinoma.

Ke-Yi Li, Jie Zhang, Li-Cheng Jiang, Bin Zhang, Chun-Peng Xia, Kai Xu, Hai-Ying Chen, Qiao-Zhi Yang, Shu-Wei Liu, Hong Zhu

RetractedAbstract readRetracted Publication
In one paragraph

Article in Cancer biomarkers : section A of Disease markers, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.7field-weighted citation impact, top 27% 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

8 citing papers in PubMed, 13 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

Ke-Yi LiDepartment of Anatomy, Shandong University School of Medicine, Jinan, Shandong, China.
Jie ZhangDepartment of Pathology, Liaocheng People's Hospital, Liaocheng, Shandong, China.
Li-Cheng JiangDepartment of Oral and Maxillofacial Surgery, Liaocheng People's Hospital, Liaocheng, Shandong, China.
Bin ZhangDepartment of Anatomy, Shandong University School of Medicine, Jinan, Shandong, China.
Chun-Peng XiaDepartment of Oral and Maxillofacial Surgery, Liaocheng People's Hospital, Liaocheng, Shandong, China.
Kai XuDepartment of Oral and Maxillofacial Surgery, Liaocheng People's Hospital, Liaocheng, Shandong, China.
Hai-Ying ChenKey Lab of Oral and Maxillofacial Medicine, Liaocheng People's Hospital, Liaocheng, Shandong, China.
Qiao-Zhi YangDepartment of Oral and Maxillofacial Surgery, Liaocheng People's Hospital, Liaocheng, Shandong, China.
Shu-Wei LiuDepartment of Anatomy, Shandong University School of Medicine, Jinan, Shandong, China.
Hong ZhuDepartment of Stomatology, Beijing Pediatric Hospital, Beijing, China.
Liaocheng People's Hospital · CNShandong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOral squamous cell carcinoma (OSCC) is a frequently diagnosed life-threatening oral cancer worldwide and has become one of the leading causes of cancer-related mortality. However, the pathogenesis of this disease is very limited.

objectiveIn this study, we aimed to investigate the functional relationship between OSCC and a potential tumor related gene ubiquitin-specific proteases 39 (USP39).

methodsThe lentivirus-based RNA interference was utilized to knock down USP39 expression in human OSCC CAL27 cells. The effect of USP39 on cell proliferation was detected by MTT and colony formation assays.

resultsThe results uncovered that the proliferation rate was significantly decreased in specific USP39-targeting lentivirus infected cells compared to control lentivirus infected cells. The colony formation capacity was also attenuated in CAL27 cells after USP39 knockdown. Moreover, knockdown of USP39 arrested CAL27 cells in S and G1/M phases of the cell cycle. Furthermore, USP39 silencing induced apoptosis of CAL27 cells via activations of Caspase 3 and PARP.

conclusionsIn conclusion, the inhibition of USP39 in CAL27 cells suppressed cell growth probably via induction cell cycle arrest and apoptosis. USP39 might act as an oncogenic factor in OSCC and could be a potential molecular target for OSCC gene therapy.

Indexed as

RNA InterferenceApoptosisCarcinoma, Squamous CellCell CycleCell Line, TumorCell ProliferationGene Knockdown TechniquesGene SilencingGenetic VectorsHumansLentivirusMouth NeoplasmsRNA, Small InterferingUbiquitin-Specific ProteasesRNA, Small InterferingUbiquitin-Specific ProteasesUSP39 protein, humanDrug targetoral squamous cell carcinomaRNA interferenceubiquitin-specific proteases 39

Identifiers

PMID26835714
PMCPMC13016538
OpenAlexW2182985743

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.