Evidence map›Paper›PMID 25902835›Full record

ArticleBMB reports2015

DEPDC1 is a novel cell cycle related gene that regulates mitotic progression.

Yan Mi, Chundong Zhang, Youquan Bu, Ying Zhang, Longxia He, Hongxia Li, Huifang Zhu, Yi Li, Yunlong Lei, Jiang Zhu

Open access · goldAbstract read
In one paragraph

Article in BMB reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 11% 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

33 citing papers in PubMed, 1 synthesis or guideline pooled it, 61 citations in OpenAlex.

  1. Pooled it
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  19. Toxicity of TiOInternational journal of molecular sciences · 2020
    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 1 institution in 1 country.

Yan MiDepartment of Otolaryngology, The First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, China.
Chundong ZhangDepartment of Biochemistry and Molecular Biology, Chongqing Medical University; Molecular Medicine and Cancer Research Center, Chongqing Medical University, Chongqing 400016, China.
Youquan BuDepartment of Biochemistry and Molecular Biology, Chongqing Medical University; Molecular Medicine and Cancer Research Center, Chongqing Medical University, Chongqing 400016, China.
Ying ZhangDepartment of Biochemistry and Molecular Biology, Chongqing Medical University; Molecular Medicine and Cancer Research Center, Chongqing Medical University, Chongqing 400016, China.
Longxia HeDepartment of Otolaryngology, The First Affiliated Hospital of Chongqing Medical University; Molecular Medicine and Cancer Research Center, Chongqing Medical University, Chongqing 400016, China.
Hongxia LiDepartment of Otolaryngology, The First Affiliated Hospital of Chongqing Medical University; Molecular Medicine and Cancer Research Center, Chongqing Medical University, Chongqing 400016, China.
Huifang ZhuDepartment of Biochemistry and Molecular Biology, Chongqing Medical University; Molecular Medicine and Cancer Research Center, Chongqing Medical University, Chongqing 400016, China.
Yi LiDepartment of Biochemistry and Molecular Biology, Chongqing Medical University; Molecular Medicine and Cancer Research Center, Chongqing Medical University, Chongqing 400016, China.
Yunlong LeiDepartment of Biochemistry and Molecular Biology, Chongqing Medical University; Molecular Medicine and Cancer Research Center, Chongqing Medical University, Chongqing 400016, China.
Jiang ZhuDepartment of Otolaryngology, The First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, China.
Chongqing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

DEPDC1 is a recently identified novel tumor-related gene that is upregulated in several types of cancer and contributes to tumorigenesis. In this study, we have investigated the expression pattern and functional implications of DEPDC1 during cell cycle progression. Expression studies using synchronized cells demonstrated that DEPDC1 is highly expressed in the mitotic phase of the cell cycle. Immunofluorescence assays showed that DEPDC1 is predominantly localized in the nucleus during interphase and is redistributed into the whole cell upon nuclear membrane breakdown in metaphase. Subsequently, siRNA-mediated knockdown of DEPDC1 caused a significant mitotic arrest. Moreover, knockdown of DEPDC1 resulted in remarkable mitotic defects such as abnormal multiple nuclei and multipolar spindle structures accompanied by the upregulation of the A20 gene as well as several cell cycle-related genes such as CCNB1 and CCNB2. Taken together, our current observations strongly suggest that this novel cancerous gene, DEPDC1, plays a pivotal role in the regulation of proper mitotic progression.

Indexed as

Cell Cycle CheckpointsCentrosomeDNA-Binding ProteinsFluorescent Antibody TechniqueGene Knockdown TechniquesGTPase-Activating ProteinsHeLa CellsHumansIntracellular Signaling Peptides and ProteinsMitosisNeoplasm ProteinsNuclear ProteinsProtein TransportRNA, Small InterferingSubcellular FractionsTumor Necrosis Factor alpha-Induced Protein 3DEPDC1 protein, humanDNA-Binding ProteinsGTPase-Activating ProteinsIntracellular Signaling Peptides and ProteinsNeoplasm ProteinsNuclear ProteinsRNA, Small InterferingTNFAIP3 protein, humanTumor Necrosis Factor alpha-Induced Protein 3

Identifiers

PMID25902835
PMCPMC4577292
OpenAlexW2296717069

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.