Evidence map›Paper›PMID 30485574›Full record

ArticleCell proliferation2019

CSE1L participates in regulating cell mitosis in human seminoma.

Chunyan Liu, Jiajing Wei, Kang Xu, Xiaosong Sun, Huiping Zhang, Chengliang Xiong

Open access · hybridAbstract read
In one paragraph

Article in Cell proliferation, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

14 citing papers in PubMed, 17 citations in OpenAlex.

  1. CSE1L Silencing Enhances Cytarabine-mediated Cytotoxicity in Acute Myeloid Leukemia.Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion · 2024
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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

6 authors at 4 institutions in 1 country.

Chunyan LiuFamily Planning Research Institute, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.ORCID http://orcid.org/0000-0003-4322-3063
Jiajing WeiFamily Planning Research Institute, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Kang XuThe First People's Hospital of Tianmen City, Tianmen, China.
Xiaosong SunXiangyang Central Hospital, Affiliated Hospital of Hubei University of Arts and Science, Xiangyang, China.
Huiping ZhangFamily Planning Research Institute, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Chengliang XiongFamily Planning Research Institute, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Huazhong University of Science and Technology · CNTongji Hospital · CNHubei University of Arts and Science · CNThe First People's Hospital of Tianmen · CN

Funding

The China Postdoctoral Science Foundation 2016M600597the Fundamental Research Funds for the Central Universities 2016YXMS163the National Natural Science Foundation of China 81601282
6 · The paper itself

Abstract

objectivesCSE1L has been reported to be highly expressed in various tumours. Testicular germ cell tumours are common among young males, and seminoma is the major type. However, whether CSE1L has functions in the seminoma is unclear. MATERIALS AND

methodsThe expression of CSE1L was detected by immunohistochemistry in seminoma tissues and non-tumour normal testis tissues from patients. CSE1L distribution during cell mitosis was determined by immunofluorescent staining with CSE1L, α-tubulin and γ-tubulin antibodies. The effects of Cse1L knockdown on cell proliferation and cell cycle progression were determined by Cell Counting Kit-8 assay, flow cytometry, PH3 staining and bromodeoxyuridine incorporation assay.

resultsCSE1L was significantly enriched in the seminoma tissue compared with the non-tumour normal testis tissue. CSE1L also co-localized with α-tubulin in the cells with a potential to divide. In the seminoma cell line TCam-2, CSE1L was associated with the spindles and the centrosomes during cell division. The knockdown of CSE1L in TCam-2 cells attenuated the cells' proliferative capacity. Cell cycle assay revealed that the CSE1L-deficient cells were mainly arrested in the G0/G1 phase and moderately delayed in the G2/M phase. The proportion of cells with multipolar spindle and abnormal spindle geometry was obviously increased by CSE1L expression silencing in the TCam-2 cells.

conclusionsOverall, these findings showed that CSE1L plays a pivotal role in maintaining cell proliferation and cell division in seminomas.

Indexed as

MitosisCell CycleCell Line, TumorCell ProliferationCellular Apoptosis Susceptibility ProteinGene DeletionHumansMaleSeminomaTesticular NeoplasmsTestisCellular Apoptosis Susceptibility Proteincell mitosiscell proliferationCSE1Lseminomaspindle

Identifiers

PMID30485574
PMCPMC6496685
OpenAlexW2902866774

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.