Evidence map›Paper›PMID 31199049›Full record

ArticleMolecular oncology2019

Aberrantly expressed PLOD1 promotes cancer aggressiveness in bladder cancer: a potential prognostic marker and therapeutic target.

Yasutaka Yamada, Mayuko Kato, Takayuki Arai, Hiroki Sanada, Akifumi Uchida, Shunsuke Misono, Shinichi Sakamoto, Akira Komiya, Tomohiko Ichikawa, Naohiko Seki

Open access · goldAbstract read
In one paragraph

Article in Molecular oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
4.3field-weighted citation impact, top 5% 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

24 citing papers in PubMed, 62 citations in OpenAlex.

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  16. Integrated Profiling IdentifiesFrontiers in immunology · 2021
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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 2 institutions in 1 country.

Yasutaka YamadaDepartment of Functional Genomics, Chiba University Graduate School of Medicine, Japan.
Mayuko KatoDepartment of Functional Genomics, Chiba University Graduate School of Medicine, Japan.
Takayuki AraiDepartment of Functional Genomics, Chiba University Graduate School of Medicine, Japan.
Hiroki SanadaDepartment of Pulmonary Medicine, Graduate School of Medical and Dental Sciences, Kagoshima University, Japan.
Akifumi UchidaDepartment of Pulmonary Medicine, Graduate School of Medical and Dental Sciences, Kagoshima University, Japan.
Shunsuke MisonoDepartment of Pulmonary Medicine, Graduate School of Medical and Dental Sciences, Kagoshima University, Japan.
Shinichi SakamotoDepartment of Urology, Chiba University Graduate School of Medicine, Japan.
Akira KomiyaDepartment of Urology, Chiba University Graduate School of Medicine, Japan.
Tomohiko IchikawaDepartment of Urology, Chiba University Graduate School of Medicine, Japan.
Naohiko SekiDepartment of Functional Genomics, Chiba University Graduate School of Medicine, Japan.
Chiba University · JPKagoshima University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bladder cancer (BC) is the ninth most malignant tumor worldwide. Some BC patients will develop muscle-invasive BC (MIBC), which has a 5-year survival rate of approximately 60% due to metastasis. As such, there is an urgent need for novel therapeutic and diagnostic targets for MIBC. Analysis of novel antitumor microRNA (miRNA)-mediated cancer networks is an effective strategy for exploring therapeutic targets and prognostic markers in cancers. Our previous miRNA analysis revealed that miR-140-5p acts as an antitumor miRNA in BC cells. Here, we investigated miR-140-5p regulation of BC molecular pathogenesis. Procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1 (PLOD1) was found to be directly regulated by miR-140-5p, and aberrant expression of PLOD1 was observed in BC clinical specimens. High PLOD1 expression was significantly associated with a poor prognosis (disease-free survival: P = 0.0204; overall survival: P = 0.000174). Multivariate analysis showed PLOD1 expression to be an independent prognostic factor in BC patients (hazard ratio = 1.51, P = 0.0099). Furthermore, downregulation of PLOD1 by siRNAs and a specific inhibitor significantly decreased BC cell aggressiveness. Aberrant expression of PLOD1 was closely associated with BC pathogenesis. In summary, the present study showed that PLOD1 may be a potential prognostic marker and therapeutic target for BC.

Indexed as

Gene Expression Regulation, DevelopmentalGene Expression Regulation, NeoplasticBiomarkers, TumorCell Line, TumorDisease-Free SurvivalFemaleHumansMaleMicroRNAsNeoplasm ProteinsProcollagen-Lysine, 2-Oxoglutarate 5-DioxygenaseRNA, NeoplasmSurvival RateUrinary Bladder NeoplasmsBiomarkers, TumorMicroRNAsMirn140 microRNA, humanNeoplasm ProteinsPLOD1 protein, humanProcollagen-Lysine, 2-Oxoglutarate 5-DioxygenaseRNA, Neoplasmbladder cancerinhibitormicroRNAmiR-140-5ppassenger strandPLOD1

Identifiers

PMID31199049
PMCPMC6717764
OpenAlexW2951611253

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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.