Evidence map›Paper›PMID 26539909›Full record

ArticleCell death & disease2015

Downregulation of miR-320a/383-sponge-like long non-coding RNA NLC1-C (narcolepsy candidate-region 1 genes) is associated with male infertility and promotes testicular embryonal carcinoma cell proliferation.

M Lü, H Tian, Y-X Cao, X He, L Chen, X Song, P Ping, H Huang, F Sun

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

57 citing papers in PubMed, 84 citations in OpenAlex.

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  12. LncRNA Fendrr: involvement in the protective role of nucleolin against HRedox report : communications in free radical research · 2023
    Article
  13. Epigenetic Factors and ncRNAs in Testicular Cancer.International journal of molecular sciences · 2023
    Review
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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 6 institutions in 1 country.

M LüInternational Peace Maternity & Child Health Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai, China.
H TianInternational Peace Maternity & Child Health Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai, China.
Y-X CaoReproduction Medical Center, Department of Obstetrics and Gynecology, the First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.
X HeReproduction Medical Center, Department of Obstetrics and Gynecology, the First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.
L ChenInstitute of Biochemistry and Cell Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai, China.
X SongSchool of Life Sciences, University of Science and Technology of China, Hefei, Anhui, China.
P PingRenji Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai, China.
H HuangInternational Peace Maternity & Child Health Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai, China.
F SunInternational Peace Maternity & Child Health Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai, China.
International Peace Maternity & Child Health Hospital · CNAnhui Medical University · CNCenter for Excellence in Molecular Cell Science · CNFirst Affiliated Hospital of Anhui Medical University · CNRenji Hospital · CNUniversity of Science and Technology of China · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Long non-coding RNAs (lncRNAs), which are extensively transcribed from the genome, have been proposed to be key regulators of diverse biological processes. However, little is known about the role of lncRNAs in regulating spermatogenesis in human males. Here, using microarray technology, we show altered expression of lncRNAs in the testes of infertile men with maturation arrest (MA) or hypospermatogenesis (Hypo), with 757 and 2370 differentially down-regulated and 475 and 163 up-regulated lncRNAs in MA and Hypo, respectively. These findings were confirmed by quantitative real-time PCR (qRT-PCR) assays on select lncRNAs, including HOTTIP, imsrna320, imsrna292 and NLC1-C (narcolepsy candidate-region 1 genes). Interestingly, NLC1-C, also known as long intergenic non-protein-coding RNA162 (LINC00162), was down-regulated in the cytoplasm and accumulated in the nucleus of spermatogonia and primary spermatocytes in the testes of infertile men with mixed patterns of MA compared with normal control. The accumulation of NLC1-C in the nucleus repressed miR-320a and miR-383 transcript and promoted testicular embryonal carcinoma cell proliferation by binding to Nucleolin. Here, we define a novel mechanism by which lncRNAs modulate miRNA expression at the transcriptional level by binding to RNA-binding proteins to regulate human spermatogenesis.

Indexed as

AdultCarcinoma, EmbryonalCase-Control StudiesCell ProliferationDown-RegulationEmbryonal Carcinoma Stem CellsHumansInfertility, MaleMaleMicroRNAsMiddle AgedNeoplasms, Germ Cell and EmbryonalNucleolinPhosphoproteinsRNA-Binding ProteinsRNA, Long NoncodingMicroRNAsMIRN320 microRNA, humanMIRN383 microRNA, humanNLC1C lncRNA, humanNucleolinPhosphoproteinsRNA-Binding ProteinsRNA, Long Noncoding

Identifiers

PMID26539909
PMCPMC4670917
OpenAlexW2210113090

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.