Evidence map›Paper›PMID 29915327›Full record

ArticleCell death & disease2018

Long intergenic non-coding RNA 00324 promotes gastric cancer cell proliferation via binding with HuR and stabilizing FAM83B expression.

Zigui Zou, Tianshi Ma, Xuezhi He, Jinxing Zhou, Hongwei Ma, Min Xie, Yanhua Liu, Die Lu, Shihao Di, Zhihong Zhang

Erratum issuedAbstract read
In one paragraph

Article in Cell death & disease, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 66 papers.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed
–field-weighted citation impact
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

66 citing papers in PubMed.

  1. Review
  2. Article
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  5. Review
  6. Article
  7. Article
  8. Article
  9. Relationship between HuR and tumor drug resistance.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2023
    Review
  10. Article
  11. Review
  12. Long non-coding RNAs involved in retinoblastoma.Journal of cancer research and clinical oncology · 2023
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

6 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Zigui Zou *Department of Pathology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Tianshi Ma *Department of Pathology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Xuezhi HeDepartment of Anatomy, Histology and Embryology, Research Centre for Bone and Stem Cells, Nanjing Medical University, Nanjing, China.
Jinxing ZhouDepartment of Pathology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Hongwei MaDepartment of Pathology, Zhenjiang First people's hospital, Zhenjiang, China.
Min XieCentral Laboratory, Suzhou Municipal Hospital, Nanjing Medical University Affiliated Suzhou Hospital, Suzhou, China.
Yanhua LiuDepartment of Oncology, Affiliated Xuzhou Central Hospital, Xuzhou Medical College, Xuzhou, China.
Die LuDepartment of Pathology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Shihao DiDepartment of Pathology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Zhihong ZhangDepartment of Pathology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China. zhangzh@njmu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Substantial evidence shows that long non-coding RNAs (lncRNAs) participate in many biological mechanisms, and their dysregulation are also involved in the development and progression of cancers, including gastric cancer (GC). Long intergenic non-coding RNA 00324 (LINC00324), a 2115 bp ncRNA, is located on chromosome 17p13.1. The biological function and molecular mechanisms of LINC00324 in GC remains undiscovered. In this paper, we found that the expression level of LINC00324 was significantly upregulated in GC tissues compared with the corresponding normal tissues. The overexpression of LINC00324 was correlated with advanced TNM stage, larger tumor size, and lymph node metastasis as well as poor prognosis. Further experiments revealed that knockdown of LINC00324 could suppress the proliferation of GC cells. RNA transcriptome sequencing technology revealed that FAM83B may be a significant downstream target gene of LINC00324. LINC00324 could combine with the RNA-binding protein (RBP) human antigen R (HuR) and thus stabilize the expression of FAM83B. Moreover, rescue assays showed that the reduced FAM83B expression partially reversed the promotion of cell growth in GC induced by the overexpression of LINC00324. In conclusion, our study revealed that LINC00324 acted as an oncogene in tumorigenesis and progression, suggesting that it could be a new biomarker in diagnosis and prognosis of GC.

Indexed as

AnimalsCell ProliferationCells, CulturedCell Transformation, NeoplasticDisease ProgressionDNA, IntergenicELAV-Like Protein 1Gene Expression Regulation, NeoplasticHumansLymphatic MetastasisMaleMiceMice, Inbred BALB CMice, NudeNeoplasm ProteinsProtein BindingDNA, IntergenicELAV-Like Protein 1FAM83B protein, humanNeoplasm ProteinsRNA, Long Noncoding

Identifiers

PMID29915327
PMCPMC6006375

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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.