Evidence map›Paper›PMID 30609030›Full record

ArticleJournal of cellular physiology2019

Microarray expression profiles analysis revealed lncRNA OXCT1-AS1 promoted bladder cancer cell aggressiveness via miR-455-5p/JAK1 signaling.

Jin-Bo Chen, Ye-Wen Zhu, Xi Guo, Cui Yu, Pei-Hua Liu, Chao Li, Jiao Hu, Hui-Huang Li, Long-Fei Liu, Min-Feng Chen and 2 more

Abstract read
In one paragraph

Article in Journal of cellular physiology, 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
2.0field-weighted citation impact, top 14% 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, 35 citations in OpenAlex.

  1. Review
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  7. Comprehensive analysis of ERCC3 prognosis value and ceRNA network in AML.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2023
    Article
  8. LncRNATranslational cancer research · 2022
    Article
  9. Article
  10. mTheranostics · 2022
    Article
  11. Review
  12. Article
  13. Role of Long Non-coding RNAs on Bladder Cancer.Frontiers in cell and developmental biology · 2021
    Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. 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

12 authors at 1 institution in 2 countries.

Jin-Bo ChenDepartment of Urology, Xiangya Hospital, Central South University, Changsha, China.
Ye-Wen ZhuDepartment of Urology, Xiangya Hospital, Central South University, Changsha, China.
Xi GuoDepartment of Urology, Xiangya Hospital, Central South University, Changsha, China.
Cui YuDepartment of Urology, Xiangya Hospital, Central South University, Changsha, China.ORCID 0000-0002-9608-8996
Pei-Hua LiuDepartment of Urology, Xiangya Hospital, Central South University, Changsha, China.
Chao LiDepartment of Urology, Xiangya Hospital, Central South University, Changsha, China.
Jiao HuDepartment of Urology, Xiangya Hospital, Central South University, Changsha, China.
Hui-Huang LiDepartment of Urology, Xiangya Hospital, Central South University, Changsha, China.
Long-Fei LiuDepartment of Urology, Xiangya Hospital, Central South University, Changsha, China.
Min-Feng ChenDepartment of Urology, Xiangya Hospital, Central South University, Changsha, China.
He-Qun ChenDepartment of Urology, Xiangya Hospital, Central South University, Changsha, China.
Zu Xiong-BingDepartment of Urology, Xiangya Hospital, Central South University, Changsha, China.
Central South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bladder cancer (BCa) is one of the most prevalent cancers of the urinary system worldwide. Accumulating evidence suggests that long noncoding RNAs (lncRNAs) perform a vital function in the pathogenesis and progression of BCa. In the current study, we identified a novel lncRNA OXCT1-AS1 and investigated its role and potential mechanisms in BCa. The microarray results showed the expression of lncRNAs, microRNAs, and messenger RNAs between BCa primary tumor tissues and metastatic lymph nodes were significantly different. The quantitative polymerase chain reaction verification was performed to ensure the reliability of the screening results. The Cell Counting Kit 8 and transwell assay were used to assess the tumor cell proliferation and invasion abilities in vitro, respectively. The dual-luciferase activity assay was performed to investigate the potential mechanism of competing endogenous RNA network. lncRNA OXCT1-AS1, which elevated in metastasis lymph node, was significantly upregulated in BCa cell lines compared with SVHUC-1. We demonstrated OXCT1-AS1 inhibited miR-455-5p to decrease its binding to the JAK1 3'-untranslated region, which could upregulate the expression of JAK1 at the protein level, thus promoting BCa proliferation and invasion. Therefore, lncRNA OXCT1-AS1 could act as a potential biomarker and therapeutic target for patients with BCa.

Indexed as

Cell ProliferationGene Expression ProfilingGene Expression Regulation, NeoplasticHumansJanus Kinase 1MicroRNAsOligonucleotide Array Sequence AnalysisRNA, Long NoncodingSignal TransductionUrinary Bladder NeoplasmsJAK1 protein, humanJanus Kinase 1MicroRNAsMIRN455 microRNA, humanRNA, Long Noncodingbladder cancer (BCa)competing endogenous RNA (ceRNA)long noncoding RNA (lncRNA)OXCT1-AS1

Identifiers

PMID30609030
PMCPMC13483269
OpenAlexW2906950171

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.